---
OA_place: publisher
_id: '19903'
abstract:
- lang: eng
  text: "Cooperation, that is, one person paying a cost for another's benefit, is
    a fundamental principle without which no form of society could exist. The extent
    to which humans cooperate with each other is also an essential feature that differentiates
    them from other animals. Cooperation occurs even in the absence of altruistic
    motivations, when it is selfishly incentivised by the expectation of a future
    reward. For example, many economic interactions are well described that way. This
    kind of cooperation requires that people exhibit reciprocal behaviour that acts
    as a mechanism that rewards cooperation.\r\nWith game-theoretic models, it is
    possible to formally study potential such mechanisms and under what conditions
    they can exist. This thesis contributes to this effort by analysing recently introduced
    models of cooperation that advance on previous work by taking into account the
    potential for pre-existing inequality among cooperating individuals as well as
    the different forms that reciprocity can take.\r\nIndividuals may differ both
    intrinsically, in their abilities, as well as extrinsically, in the amount of
    resources they have available. Allowing for such differences in a model of cooperation
    helps to understand how inequality affects the potential for, and outcomes of,
    cooperation among unequals. In this thesis, it is shown that in the presence of
    intrinsic inequality, a similar unequal distribution of resources can increase
    the potential for cooperation. This effect is stronger the smaller the group is
    in which cooperation takes place. It is also shown that under particular assumptions,
    if the unequal members of a group vary the size of their contributions to a cooperative
    effort over time, they can thereby increase their efficiency and improve the collective
    outcome.\r\nCooperative behaviour in a two-person interaction can be rewarded
    either by direct reciprocation whenever the same two people interact again, or
    indirectly by a third party who observed the interaction. In the latter case of
    indirect reciprocity, individuals are proximally rewarded by a good reputation,
    which ultimately translates to being rewarded with cooperative behaviour by others.
    This mechanism can enable selfishly motivated cooperation even in circumstances
    where individuals are unlikely to meet again, akin to how money facilitates trade.
    While these two forms of reciprocity have mostly been studied in isolation, this
    thesis analyses both direct and indirect reciprocity in a general model in order
    to compare their relative effectiveness under different circumstances. The contribution
    of this thesis is an extension of previous work regarding a specific kind of interaction,
    whose parameters allow for convenient mathematical analysis, to the most general
    set of possible interactions."
acknowledgement: "The research for this thesis was supported by the European Research
  Council\r\n(grant agreements No. 863818 and No. 850529), the European Union’s Horizon
  2020 research and innovation programme (Marie Skłodowska-Curie grant agreement No.
  754411),\r\nthe Austrian Science Fund (grant DOI 10.55776/COE12), the French Agence
  Nationale\r\nde la Recherche under the Programme d’investissements d’avenir (project
  reference 17-\r\nEURE-0010) and the Australian Government through the Australian
  Research Council\r\n(grant No. SR200100005, “Securing Antarctica’s Environmental
  Future”)."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Valentin
  full_name: Hübner, Valentin
  id: 2c8aa207-dc7d-11ea-9b2f-f22972ecd910
  last_name: Hübner
  orcid: 0009-0001-5009-4987
citation:
  ama: Hübner V. Reciprocity and inequality in social dilemmas. 2025. doi:<a href="https://doi.org/10.15479/AT-ISTA-19903">10.15479/AT-ISTA-19903</a>
  apa: Hübner, V. (2025). <i>Reciprocity and inequality in social dilemmas</i>. Institute
    of Science and Technology Austria. <a href="https://doi.org/10.15479/AT-ISTA-19903">https://doi.org/10.15479/AT-ISTA-19903</a>
  chicago: Hübner, Valentin. “Reciprocity and Inequality in Social Dilemmas.” Institute
    of Science and Technology Austria, 2025. <a href="https://doi.org/10.15479/AT-ISTA-19903">https://doi.org/10.15479/AT-ISTA-19903</a>.
  ieee: V. Hübner, “Reciprocity and inequality in social dilemmas,” Institute of Science
    and Technology Austria, 2025.
  ista: Hübner V. 2025. Reciprocity and inequality in social dilemmas. Institute of
    Science and Technology Austria.
  mla: Hübner, Valentin. <i>Reciprocity and Inequality in Social Dilemmas</i>. Institute
    of Science and Technology Austria, 2025, doi:<a href="https://doi.org/10.15479/AT-ISTA-19903">10.15479/AT-ISTA-19903</a>.
  short: V. Hübner, Reciprocity and Inequality in Social Dilemmas, Institute of Science
    and Technology Austria, 2025.
corr_author: '1'
date_created: 2025-06-25T13:50:10Z
date_published: 2025-06-25T00:00:00Z
date_updated: 2026-10-15T10:10:25Z
day: '25'
ddc:
- '519'
degree_awarded: PhD
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- _id: KrCh
doi: 10.15479/AT-ISTA-19903
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- iso: eng
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month: '06'
oa: 1
oa_version: Published Version
page: '157'
project:
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: 4029cfc7-b034-11f1-9e55-88ab2ff3b6ee
  grant_number: COE12
  name: Bilateral Artificial Intelligence (Chatterjee)
publication_identifier:
  issn:
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publication_status: published
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- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
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---
OA_place: publisher
_id: '20138'
abstract:
- lang: eng
  text: "The evolution shapes the world around us.\r\nNot only in biology, where the
    fittest individuals spread their genes but also in physics and social dynamics,
    the evolutionary forces determine the development of a state of matter or public
    opinions.\r\nMany models describe these dynamics.\r\nThis thesis examines the
    role of the structure in the models of selection.\r\nThe population structure
    is represented as a graph or a network, and each vertex is occupied by one individual.\r\nEvery
    individual has a type and fitness that represents the reproductive potential and
    depends on the type, occupied vertex, and the arrangement of the neighbors.\r\nThe
    evolution is modeled in discrete steps; in one step, one individual is replaced
    by a neighbor selected randomly with the influence of fitness.\r\n\r\n\r\n\r\nThe
    role of the networks is widely examined in the literature.\r\nThe structures that
    promote the spread of the desired type compared to the structureless case are
    called amplifiers.\r\nThe existence of amplifiers in various settings is an intensively
    studied topic, and in some settings, the amplifiers have been identified.\r\nMoreover,
    there are other important questions about the number of steps until one type spreads
    over the whole network (fixation time), the computational complexity, and the
    questions about the robustness of these processes.\r\n\r\n\r\nThis thesis explores
    the role of structure in evolution from many perspectives.\r\nFirst, it introduces
    different models and various choices that can be made in the models of evolution.\r\nIt
    highlights the role of the structure in the real world and how this is reflected
    in these models.\r\nThen, it describes the previous results and open problems.\r\nSecond,
    the thesis describes an amplifier for two variants of the Moran process: one with
    a constant birth rate and the other with a constant death rate.\r\nThis is an
    important contribution to the robustness of the amplification.\r\nThird, the thesis
    determines the complexity of spatial games.\r\nThese are processes where the fitness
    comes from a game, and the strength of selection is high.\r\nIt shows that determining
    the fate of cooperation in these games is a PSPACE-complete problem.\r\nFourth,
    the thesis describes the amplifier of cooperation for spatial games.\r\nThis is
    the first amplifier in this setting.\r\nFifth, the thesis examines the coexistence
    in the Moran process with environmental heterogeneity.\r\nIn this setting, the
    fitness depends not only on the type of the individual but also on the occupied
    vertex.\r\nThe chapter determines the relationship between the interactions of
    vertices of different types and the coexistence time.\r\nSixth, the thesis examines
    the social balance on networks and proposes a stochastic dynamic partially aware
    of the state of the graph, which reaches a balanced position quickly.\r\nFinally,
    the thesis presents conclusions and outlines the directions for future work.\r\n\r\n\r\n"
acknowledgement: "This work was supported by the European Research Council CoG 863818
  (ForMSMArt) and Austrian Science Fund 10.55776/COE12.\r\n"
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Jakub
  full_name: Svoboda, Jakub
  id: 130759D2-D7DD-11E9-87D2-DE0DE6697425
  last_name: Svoboda
  orcid: 0000-0002-1419-3267
citation:
  ama: Svoboda J. Structural properties of games on graphs. 2025. doi:<a href="https://doi.org/10.15479/AT-ISTA-20138">10.15479/AT-ISTA-20138</a>
  apa: Svoboda, J. (2025). <i>Structural properties of games on graphs</i>. Institute
    of Science and Technology Austria. <a href="https://doi.org/10.15479/AT-ISTA-20138">https://doi.org/10.15479/AT-ISTA-20138</a>
  chicago: Svoboda, Jakub. “Structural Properties of Games on Graphs.” Institute of
    Science and Technology Austria, 2025. <a href="https://doi.org/10.15479/AT-ISTA-20138">https://doi.org/10.15479/AT-ISTA-20138</a>.
  ieee: J. Svoboda, “Structural properties of games on graphs,” Institute of Science
    and Technology Austria, 2025.
  ista: Svoboda J. 2025. Structural properties of games on graphs. Institute of Science
    and Technology Austria.
  mla: Svoboda, Jakub. <i>Structural Properties of Games on Graphs</i>. Institute
    of Science and Technology Austria, 2025, doi:<a href="https://doi.org/10.15479/AT-ISTA-20138">10.15479/AT-ISTA-20138</a>.
  short: J. Svoboda, Structural Properties of Games on Graphs, Institute of Science
    and Technology Austria, 2025.
corr_author: '1'
das_tickbox: '1'
date_created: 2025-08-05T14:33:59Z
date_published: 2025-08-05T00:00:00Z
date_updated: 2026-10-16T08:00:05Z
day: '05'
ddc:
- '000'
- '519'
degree_awarded: PhD
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license: https://creativecommons.org/licenses/by-nc-sa/4.0/
month: '08'
oa: 1
oa_version: Published Version
page: '167'
project:
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
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  grant_number: COE12
  name: Bilateral Artificial Intelligence (Chatterjee)
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publisher_comment: "Chapter 4 is copyrighted by CC BY-NC-ND\r\n4.0, which prohibits
  derivatives. Chapter 6 is copyrighted: Copyright (2025) by the American\r\nPhysical
  Society. For a copy, redistribution, or modification needs to be permitted by the\r\nAmerican
  Physical Society.\r\n"
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  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
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  orcid: 0000-0002-4561-241X
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OA_place: publisher
_id: '20575'
abstract:
- lang: eng
  text: "This thesis deals with eigenvalue and eigenvector universality results for
    random matrix ensembles equipped with non-trivial spatial structure. We consider
    both mean-field models with a general variance profile (Wigner-type matrices)
    and correlation structure (correlated matrices) among the entries, as well as
    non-mean-field random band matrices with bandwidth W >> N^(1/2).\r\n\r\nTo extract
    the universal properties of random matrix spectra and eigenvectors, we obtain
    concentration estimates for their resolvent, the local laws, which generalize
    the celebrated Wigner semicircle law for a broad class of random matrices to much
    finer spectral scales. The local laws hold for both a single resolvent as well
    as for products of multiple resolvents, known as resolvent chains, and express
    the remarkable approximately-deterministic behavior of these objects down to the
    microscopic scale.\r\n\r\nOur primary tool for establishing the local laws is
    the dynamical Zigzag strategy, which we develop in the setting of spatially-inhomogeneous
    random matrices. Our proof method systematically addresses the challenges arising
    from non-trivial spatial structures and is robust to all types of singularities
    in the spectrum, as we demonstrate in the correlated setting. Furthermore, we
    incorporate the analysis of the deterministic resolvent chain approximations into
    the dynamical framework of the Zigzag strategy, synthesizing a unified toolkit
    for establishing multi-resolvent local laws.\r\n\r\nUsing these methods, we prove
    complete eigenvector delocalization, the Eigenstate Thermalization Hypothesis,
    and Wigner-Dyson universality in the bulk for random band matrices down to the
    optimal bandwidth W >> N^(1/2). For mean-field ensembles, we establish universality
    of local eigenvalue statistics at the cups for random matrices with correlated
    entries, and the Eigenstate Thermalization Hypothesis for Wigner-type matrices
    in the bulk of the spectrum.\r\n\r\nFinally, this thesis also contains other applications
    of the multi-resolvent local laws to spatially-inhomogeneous random matrices,
    obtained prior to the development of the Zigzag strategy. In particular, we provide
    a complete analysis of mesoscopic linear-eigenvalue statistics of Wigner-type
    matrices in all spectral regimes, including the novel cusps, and rigorously establish
    the prethermalization phenomenon for deformed Wigner matrices.\r\n\r\nThe main
    body of this thesis consists of seven research papers (listed on page xi), each
    presented in a separate chapter with its own introduction and all relevant context,
    suitable to be read independently. We ask the reader’s indulgence for the repetitions
    in the historical overviews and other minor redundancies that remain among the
    chapters as a result. The overall Introduction, preceding the chapters, provides
    a condensed, informal summary of the main ideas and concepts at the core of these
    works.\r\n"
acknowledgement: "The work comprising this thesis was supported by the ERC Advanced
  Grant \"RMTBeyond\"\r\nNo.101020331 awarded to my advisor."
alternative_title:
- ISTA Thesis
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author:
- first_name: Volodymyr
  full_name: Riabov, Volodymyr
  id: 1949f904-edfb-11eb-afb5-e2dfddabb93b
  last_name: Riabov
citation:
  ama: Riabov V. Universality in random matrices with spatial structure. 2025. doi:<a
    href="https://doi.org/10.15479/AT-ISTA-20575">10.15479/AT-ISTA-20575</a>
  apa: Riabov, V. (2025). <i>Universality in random matrices with spatial structure</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT-ISTA-20575">https://doi.org/10.15479/AT-ISTA-20575</a>
  chicago: Riabov, Volodymyr. “Universality in Random Matrices with Spatial Structure.”
    Institute of Science and Technology Austria, 2025. <a href="https://doi.org/10.15479/AT-ISTA-20575">https://doi.org/10.15479/AT-ISTA-20575</a>.
  ieee: V. Riabov, “Universality in random matrices with spatial structure,” Institute
    of Science and Technology Austria, 2025.
  ista: Riabov V. 2025. Universality in random matrices with spatial structure. Institute
    of Science and Technology Austria.
  mla: Riabov, Volodymyr. <i>Universality in Random Matrices with Spatial Structure</i>.
    Institute of Science and Technology Austria, 2025, doi:<a href="https://doi.org/10.15479/AT-ISTA-20575">10.15479/AT-ISTA-20575</a>.
  short: V. Riabov, Universality in Random Matrices with Spatial Structure, Institute
    of Science and Technology Austria, 2025.
corr_author: '1'
date_created: 2025-10-29T19:12:24Z
date_published: 2025-11-03T00:00:00Z
date_updated: 2026-10-16T08:41:47Z
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  call_identifier: H2020
  grant_number: '101020331'
  name: Random matrices beyond Wigner-Dyson-Mehta
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  issn:
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  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
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abstract:
- lang: eng
  text: "This thesis deals with several different models for complex quantum mechanical
    systems and is structured in three main parts. \r\n\t\r\nIn Part I, we study mean
    field random matrices as models for quantum Hamiltonians. Our focus lies on proving
    concentration estimates for resolvents of random matrices, so-called local laws,
    mostly in the setting of multiple resolvents. These estimates have profound consequences
    for eigenvector overlaps and thermalization problems. More concretely, we obtain,
    e.g., the optimal eigenstate thermalization hypothesis (ETH) uniformly in the
    spectrum for Wigner matrices, an optimal lower bound on non-Hermitian eigenvector
    overlaps, and prethermalization for deformed Wigner matrices.\tIn order to prove
    our novel multi-resolvent local laws, we develop and devise two main methods,
    the static Psi-method and the dynamical Zigzag strategy. \r\n\t\r\nIn Part II,
    we study Bardeen-Cooper-Schrieffer (BCS) theory, the standard mean field microscopic
    theory of superconductivity. We focus on asymptotic formulas for the characteristic
    critical temperature and energy gap of a superconductor and prove universality
    of their ratio in various physical regimes. Additionally, we investigate multi-band
    superconductors and show that inter-band coupling effects can only enhance the
    critical temperature. \r\n\t\r\nIn Part III, we study quantum lattice systems.
    On the one hand, we show a strong version of the local-perturbations-perturb-locally
    (LPPL) principle for the ground state of weakly interacting quantum spin systems
    with a uniform on-site gap. On the other hand, we introduce a notion of a local
    gap and rigorously justify response theory and the Kubo formula under the weakened
    assumption of a local gap. \r\n\t\r\nAdditionally, we discuss two classes of problems
    which do not fit into the three main parts of the thesis. These are deformational
    rigidity of Liouville metrics on the torus and relativistic toy models of particle
    creation via interior-boundary-conditions (IBCs).  "
alternative_title:
- ISTA Thesis
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  full_name: Henheik, Sven Joscha
  id: 31d731d7-d235-11ea-ad11-b50331c8d7fb
  last_name: Henheik
  orcid: 0000-0003-1106-327X
citation:
  ama: 'Henheik SJ. Modeling complex quantum systems: Random matrices, BCS theory,
    and quantum lattice systems. 2025. doi:<a href="https://doi.org/10.15479/AT-ISTA-19540">10.15479/AT-ISTA-19540</a>'
  apa: 'Henheik, S. J. (2025). <i>Modeling complex quantum systems: Random matrices,
    BCS theory, and quantum lattice systems</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/AT-ISTA-19540">https://doi.org/10.15479/AT-ISTA-19540</a>'
  chicago: 'Henheik, Sven Joscha. “Modeling Complex Quantum Systems: Random Matrices,
    BCS Theory, and Quantum Lattice Systems.” Institute of Science and Technology
    Austria, 2025. <a href="https://doi.org/10.15479/AT-ISTA-19540">https://doi.org/10.15479/AT-ISTA-19540</a>.'
  ieee: 'S. J. Henheik, “Modeling complex quantum systems: Random matrices, BCS theory,
    and quantum lattice systems,” Institute of Science and Technology Austria, 2025.'
  ista: 'Henheik SJ. 2025. Modeling complex quantum systems: Random matrices, BCS
    theory, and quantum lattice systems. Institute of Science and Technology Austria.'
  mla: 'Henheik, Sven Joscha. <i>Modeling Complex Quantum Systems: Random Matrices,
    BCS Theory, and Quantum Lattice Systems</i>. Institute of Science and Technology
    Austria, 2025, doi:<a href="https://doi.org/10.15479/AT-ISTA-19540">10.15479/AT-ISTA-19540</a>.'
  short: 'S.J. Henheik, Modeling Complex Quantum Systems: Random Matrices, BCS Theory,
    and Quantum Lattice Systems, Institute of Science and Technology Austria, 2025.'
corr_author: '1'
date_created: 2025-04-10T21:21:18Z
date_published: 2025-04-10T00:00:00Z
date_updated: 2026-10-16T08:41:47Z
day: '10'
ddc:
- '519'
degree_awarded: PhD
department:
- _id: GradSch
- _id: LaEr
doi: 10.15479/AT-ISTA-19540
doi_confirm: '1'
ec_funded: 1
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language:
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month: '04'
oa: 1
oa_version: Published Version
page: '720'
project:
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  call_identifier: H2020
  grant_number: '101020331'
  name: Random matrices beyond Wigner-Dyson-Mehta
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  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
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    relation: part_of_dissertation
    status: public
  - id: '18764'
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status: public
supervisor:
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
title: 'Modeling complex quantum systems: Random matrices, BCS theory, and quantum
  lattice systems'
tmp:
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  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
_id: '18764'
abstract:
- lang: eng
  text: We prove that a class of weakly perturbed Hamiltonians of the form H_λ= H_0
    + λW, with W being a Wigner matrix, exhibits prethermalization. That is, the time
    evolution generated by H_λ relaxes to its ultimate thermal state via an intermediate
    prethermal state with a lifetime of order λ^{-2}. Moreover, we obtain a general
    relaxation formula, expressing the perturbed dynamics via the unperturbed dynamics
    and the ultimate thermal state. The proof relies on a two-resolvent law for the
    deformed Wigner matrix H_λ.
acknowledgement: "All authors were supported by the ERC Advanced Grant “RMTBeyond”
  No. 101020331.\r\nJ.R. was additionally supported by the ERC Advanced Grant “LDRaM”
  No. 884584.\r\nWe thank Peter Reimann and Lennart Dabelow for helpful comments.
  Open access funding provided by Institute of Science and Technology (IST Austria)."
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
- first_name: Sven Joscha
  full_name: Henheik, Sven Joscha
  id: 31d731d7-d235-11ea-ad11-b50331c8d7fb
  last_name: Henheik
  orcid: 0000-0003-1106-327X
- first_name: Jana
  full_name: Reker, Jana
  id: e796e4f9-dc8d-11ea-abe3-97e26a0323e9
  last_name: Reker
- first_name: Volodymyr
  full_name: Riabov, Volodymyr
  id: 1949f904-edfb-11eb-afb5-e2dfddabb93b
  last_name: Riabov
citation:
  ama: Erdös L, Henheik SJ, Reker J, Riabov V. Prethermalization for deformed Wigner
    matrices. <i>Annales Henri Poincare</i>. 2025;26:1991-2033. doi:<a href="https://doi.org/10.1007/s00023-024-01518-y">10.1007/s00023-024-01518-y</a>
  apa: Erdös, L., Henheik, S. J., Reker, J., &#38; Riabov, V. (2025). Prethermalization
    for deformed Wigner matrices. <i>Annales Henri Poincare</i>. Springer Nature.
    <a href="https://doi.org/10.1007/s00023-024-01518-y">https://doi.org/10.1007/s00023-024-01518-y</a>
  chicago: Erdös, László, Sven Joscha Henheik, Jana Reker, and Volodymyr Riabov. “Prethermalization
    for Deformed Wigner Matrices.” <i>Annales Henri Poincare</i>. Springer Nature,
    2025. <a href="https://doi.org/10.1007/s00023-024-01518-y">https://doi.org/10.1007/s00023-024-01518-y</a>.
  ieee: L. Erdös, S. J. Henheik, J. Reker, and V. Riabov, “Prethermalization for deformed
    Wigner matrices,” <i>Annales Henri Poincare</i>, vol. 26. Springer Nature, pp.
    1991–2033, 2025.
  ista: Erdös L, Henheik SJ, Reker J, Riabov V. 2025. Prethermalization for deformed
    Wigner matrices. Annales Henri Poincare. 26, 1991–2033.
  mla: Erdös, László, et al. “Prethermalization for Deformed Wigner Matrices.” <i>Annales
    Henri Poincare</i>, vol. 26, Springer Nature, 2025, pp. 1991–2033, doi:<a href="https://doi.org/10.1007/s00023-024-01518-y">10.1007/s00023-024-01518-y</a>.
  short: L. Erdös, S.J. Henheik, J. Reker, V. Riabov, Annales Henri Poincare 26 (2025)
    1991–2033.
corr_author: '1'
das_tickbox: '0'
date_created: 2025-01-05T23:01:59Z
date_published: 2025-06-01T00:00:00Z
date_updated: 2026-10-16T08:41:47Z
day: '01'
ddc:
- '510'
department:
- _id: LaEr
doi: 10.1007/s00023-024-01518-y
ec_funded: 1
external_id:
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  - '2310.06677'
  isi:
  - '001385326500001'
file:
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file_date_updated: 2025-06-25T05:38:34Z
fulldoi: https://doi.org/10.1007/s00023-024-01518-y
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intvolume: '        26'
isi: 1
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: 1991-2033
project:
- _id: 62796744-2b32-11ec-9570-940b20777f1d
  call_identifier: H2020
  grant_number: '101020331'
  name: Random matrices beyond Wigner-Dyson-Mehta
publication: Annales Henri Poincare
publication_identifier:
  issn:
  - 1424-0637
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
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researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: yes
title: Prethermalization for deformed Wigner matrices
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 26
year: '2025'
...
---
OA_type: closed access
_id: '18707'
abstract:
- lang: eng
  text: Lead Sulfide (PbS) has garnered attention as a promising thermoelectric (TE)
    material due to its natural abundance and cost-effectiveness. However, its practical
    application is hindered by inherently high lattice thermal conductivity and low
    electrical conductivity. In this study, we address these challenges by surface
    functionalization of PbS nanocrystals using Cu2S molecular complexes-based ligand
    displacement. The molecular complexes facilitate the incorporation of Cu into
    the PbS matrix and leads to the formation of nanoscale defects, dislocations,
    and strain fields while optimizing the charge carrier transport. The structural
    modulations enhance the phonon scattering and lead to a significant reduction
    in lattice thermal conductivity of 0.60 W m−1K−1 at 867 K in the PbS-Cu2S system.
    Simultaneously, the Cu incorporation improves electrical conductivity by increasing
    both carrier concentration and mobility with carefully optimized the content of
    Cu2S molecular complexes. These synergistic modifications yield a peak figure-of-merit
    (zT) of 1.05 at 867 K for the PbS-1.0 %Cu2S sample, representing an almost twofold
    enhancement in TE performance compared to pristine PbS. This work highlights the
    effectiveness of surface treatment in overcoming the intrinsic limitations of
    PbS-based materials and presents a promising strategy for the development of high-efficiency
    TE systems.
acknowledgement: Y.L. acknowledges funding from the National Natural Science Foundation
  of China (NSFC) (Grants No. 22209034), the Innovation and Entrepreneurship Project
  of Overseas Returnees in Anhui Province (Grant No. 2022LCX002) and the Fundamental
  Research Funds for the Central Universities (JZ2024HGTB0239). M.I. acknowledges
  financial support from ISTA and the Werner Siemens Foundation. K.H.L. acknowledges
  financial support from the National Natural Science Foundation of China (NSFC) (Grant
  No. 22208293). M.H acknowledges funding from Australian Research Council (FT230100316
  and IH200100035) and iLAuNCH, Trailblazer Universities Program. L. H. and S. W.
  acknowledge the Fundamental Research Funds for the Central Universities (JZ2023HGTA0179,
  JZ2024HGTA0170).
article_processing_charge: No
article_type: original
author:
- first_name: Haibo
  full_name: Shu, Haibo
  last_name: Shu
- first_name: Mingjun
  full_name: Zhao, Mingjun
  last_name: Zhao
- first_name: Shaoqing
  full_name: Lu, Shaoqing
  last_name: Lu
- first_name: Shanhong
  full_name: Wan, Shanhong
  last_name: Wan
- first_name: Aziz
  full_name: Genç, Aziz
  last_name: Genç
- first_name: Lulu
  full_name: Huang, Lulu
  last_name: Huang
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
- first_name: Khak Ho
  full_name: Lim, Khak Ho
  last_name: Lim
- first_name: Min
  full_name: Hong, Min
  last_name: Hong
- first_name: Yu
  full_name: Liu, Yu
  id: 2A70014E-F248-11E8-B48F-1D18A9856A87
  last_name: Liu
  orcid: 0000-0001-7313-6740
citation:
  ama: Shu H, Zhao M, Lu S, et al. Influence of surface engineering on the transport
    properties of lead sulfide nanomaterials. <i>Journal of Colloid and Interface
    Science</i>. 2025;683:703-712. doi:<a href="https://doi.org/10.1016/j.jcis.2024.12.067">10.1016/j.jcis.2024.12.067</a>
  apa: Shu, H., Zhao, M., Lu, S., Wan, S., Genç, A., Huang, L., … Liu, Y. (2025).
    Influence of surface engineering on the transport properties of lead sulfide nanomaterials.
    <i>Journal of Colloid and Interface Science</i>. Elsevier. <a href="https://doi.org/10.1016/j.jcis.2024.12.067">https://doi.org/10.1016/j.jcis.2024.12.067</a>
  chicago: Shu, Haibo, Mingjun Zhao, Shaoqing Lu, Shanhong Wan, Aziz Genç, Lulu Huang,
    Maria Ibáñez, Khak Ho Lim, Min Hong, and Yu Liu. “Influence of Surface Engineering
    on the Transport Properties of Lead Sulfide Nanomaterials.” <i>Journal of Colloid
    and Interface Science</i>. Elsevier, 2025. <a href="https://doi.org/10.1016/j.jcis.2024.12.067">https://doi.org/10.1016/j.jcis.2024.12.067</a>.
  ieee: H. Shu <i>et al.</i>, “Influence of surface engineering on the transport properties
    of lead sulfide nanomaterials,” <i>Journal of Colloid and Interface Science</i>,
    vol. 683. Elsevier, pp. 703–712, 2025.
  ista: Shu H, Zhao M, Lu S, Wan S, Genç A, Huang L, Ibáñez M, Lim KH, Hong M, Liu
    Y. 2025. Influence of surface engineering on the transport properties of lead
    sulfide nanomaterials. Journal of Colloid and Interface Science. 683, 703–712.
  mla: Shu, Haibo, et al. “Influence of Surface Engineering on the Transport Properties
    of Lead Sulfide Nanomaterials.” <i>Journal of Colloid and Interface Science</i>,
    vol. 683, Elsevier, 2025, pp. 703–12, doi:<a href="https://doi.org/10.1016/j.jcis.2024.12.067">10.1016/j.jcis.2024.12.067</a>.
  short: H. Shu, M. Zhao, S. Lu, S. Wan, A. Genç, L. Huang, M. Ibáñez, K.H. Lim, M.
    Hong, Y. Liu, Journal of Colloid and Interface Science 683 (2025) 703–712.
das_tickbox: '1'
dataavailabilitystatement: Data will be made available on request.
date_created: 2024-12-29T23:01:56Z
date_published: 2025-04-01T00:00:00Z
date_updated: 2026-10-16T09:22:32Z
day: '01'
department:
- _id: MaIb
doi: 10.1016/j.jcis.2024.12.067
external_id:
  isi:
  - '001393340800001'
  pmid:
  - '39706089'
fulldoi: https://doi.org/10.1016/j.jcis.2024.12.067
intvolume: '       683'
isi: 1
language:
- iso: eng
month: '04'
oa_version: None
page: 703-712
pmid: 1
project:
- _id: 9B8F7476-BA93-11EA-9121-9846C619BF3A
  name: 'HighTE: The Werner Siemens Laboratory for the High Throughput Discovery of
    Semiconductors for Waste Heat Recovery'
publication: Journal of Colloid and Interface Science
publication_identifier:
  eissn:
  - 1095-7103
  issn:
  - 0021-9797
publication_status: published
publisher: Elsevier
quality_controlled: '1'
researchdata_availability: upon request
scopus_import: '1'
status: public
supplementarymaterial: yes
title: Influence of surface engineering on the transport properties of lead sulfide
  nanomaterials
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 683
year: '2025'
...
---
OA_type: closed access
_id: '18558'
abstract:
- lang: eng
  text: The current investigation presents a facile and cost-effective sol-gel approach
    for the synthesis of phase-pure multiferroic bismuth ferrite (BiFeO3) nanoparticles
    (BFO NPs) by using propylene glycol as a complexing agent, intended for use as
    a photocatalyst to efficiently degrade organic dyes in aqueous solutions under
    natural sunlight. Characterization techniques, including thermogravimetric analysis
    (TGA), Fourier transform infrared spectroscopy (FT-IR), and X-ray diffraction
    (XRD), elucidated a plausible reaction pathway for the formation of phase-pure
    BFO NPs. Rietveld refinement of the XRD data, in conjunction with transmission
    electron microscopy (TEM) and Raman spectroscopy, confirmed the synthesis of single-phase
    BFO NPs at 400 °C, displaying a space group of R3c and an average crystallite
    size of 25 nm. UV–visible diffuse reflectance spectroscopy revealed an absorption
    cut-off wavelength near 590 nm, corresponding to a band gap of 2.08 eV, indicating
    the capability of BFO NPs to absorb visible light within the 400–590 nm range.
    BFO NPs have shown efficient and rapid photocatalytic degradation of methylene
    blue (MB) in acidic, neutral, and basic pH conditions under natural sunlight.
    This is attributed to the intrinsic ferroelectric and ferromagnetic ordering present
    in synthesized BFO NPs which facilitates the separation and migration of photoinduced
    charges through band bending phenomena at the interface.
acknowledgement: "Simant Kumar Srivastav greatly acknowledges the University Grant
  Commission (UGC), New Delhi, India for providing BSR start-up grant to carry out
  this research work.\r\nThis research was supported by start-up grant of the University
  Grant Commission (UGC), New Delhi, India through project no F-30-500/2019 (BSR)."
article_processing_charge: No
article_type: original
author:
- first_name: Madhu
  full_name: Verma, Madhu
  last_name: Verma
- first_name: Ajay
  full_name: Kumar, Ajay
  last_name: Kumar
- first_name: Vijay Kumar
  full_name: Thakur, Vijay Kumar
  last_name: Thakur
- first_name: Akanksha
  full_name: Maurya, Akanksha
  last_name: Maurya
- first_name: Sachin
  full_name: Kumar, Sachin
  last_name: Kumar
- first_name: Saurabh
  full_name: Singh, Saurabh
  id: 12d625da-9cb3-11ed-9667-af09d37d3f0a
  last_name: Singh
  orcid: 0000-0003-2209-5269
- first_name: Simant Kumar
  full_name: Srivastav, Simant Kumar
  last_name: Srivastav
citation:
  ama: Verma M, Kumar A, Thakur VK, et al. Efficient and rapid sunlight-driven photocatalytic
    degradation of methylene blue dye using multiferroic BiFeO3 nanoparticles. <i>Journal
    of Sol-Gel Science and Technology</i>. 2025;113:356-373. doi:<a href="https://doi.org/10.1007/s10971-024-06607-2">10.1007/s10971-024-06607-2</a>
  apa: Verma, M., Kumar, A., Thakur, V. K., Maurya, A., Kumar, S., Singh, S., &#38;
    Srivastav, S. K. (2025). Efficient and rapid sunlight-driven photocatalytic degradation
    of methylene blue dye using multiferroic BiFeO3 nanoparticles. <i>Journal of Sol-Gel
    Science and Technology</i>. Springer Nature. <a href="https://doi.org/10.1007/s10971-024-06607-2">https://doi.org/10.1007/s10971-024-06607-2</a>
  chicago: Verma, Madhu, Ajay Kumar, Vijay Kumar Thakur, Akanksha Maurya, Sachin Kumar,
    Saurabh Singh, and Simant Kumar Srivastav. “Efficient and Rapid Sunlight-Driven
    Photocatalytic Degradation of Methylene Blue Dye Using Multiferroic BiFeO3 Nanoparticles.”
    <i>Journal of Sol-Gel Science and Technology</i>. Springer Nature, 2025. <a href="https://doi.org/10.1007/s10971-024-06607-2">https://doi.org/10.1007/s10971-024-06607-2</a>.
  ieee: M. Verma <i>et al.</i>, “Efficient and rapid sunlight-driven photocatalytic
    degradation of methylene blue dye using multiferroic BiFeO3 nanoparticles,” <i>Journal
    of Sol-Gel Science and Technology</i>, vol. 113. Springer Nature, pp. 356–373,
    2025.
  ista: Verma M, Kumar A, Thakur VK, Maurya A, Kumar S, Singh S, Srivastav SK. 2025.
    Efficient and rapid sunlight-driven photocatalytic degradation of methylene blue
    dye using multiferroic BiFeO3 nanoparticles. Journal of Sol-Gel Science and Technology.
    113, 356–373.
  mla: Verma, Madhu, et al. “Efficient and Rapid Sunlight-Driven Photocatalytic Degradation
    of Methylene Blue Dye Using Multiferroic BiFeO3 Nanoparticles.” <i>Journal of
    Sol-Gel Science and Technology</i>, vol. 113, Springer Nature, 2025, pp. 356–73,
    doi:<a href="https://doi.org/10.1007/s10971-024-06607-2">10.1007/s10971-024-06607-2</a>.
  short: M. Verma, A. Kumar, V.K. Thakur, A. Maurya, S. Kumar, S. Singh, S.K. Srivastav,
    Journal of Sol-Gel Science and Technology 113 (2025) 356–373.
das_tickbox: '1'
dataavailabilitystatement: No datasets were generated or analyzed during the current
  study.
date_created: 2024-11-17T23:01:47Z
date_published: 2025-02-01T00:00:00Z
date_updated: 2026-10-16T09:21:57Z
day: '01'
department:
- _id: MaIb
doi: 10.1007/s10971-024-06607-2
external_id:
  isi:
  - '001348590700001'
fulldoi: https://doi.org/10.1007/s10971-024-06607-2
intvolume: '       113'
isi: 1
language:
- iso: eng
month: '02'
oa_version: None
page: 356-373
publication: Journal of Sol-Gel Science and Technology
publication_identifier:
  eissn:
  - 1573-4846
  issn:
  - 0928-0707
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
researchdata_availability: not applicable
scopus_import: '1'
status: public
supplementarymaterial: yes
title: Efficient and rapid sunlight-driven photocatalytic degradation of methylene
  blue dye using multiferroic BiFeO3 nanoparticles
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 113
year: '2025'
...
---
OA_type: closed access
_id: '18701'
abstract:
- lang: eng
  text: We developed in-situ engineered polycrystalline polythiophene (PTh) and its
    composite with reduced graphene oxide (PTh-rGO) via a simple chemical synthesis.
    The PTh-rGO-based electrodes in a symmetrical device with xanthan gum in 1 M aq.
    Na2SO4 as an electrolyte, delivers a specific capacitance (Csp) of 114.7 F g–1
    (electrode) and 28.7 F g–1 (cell) at an applied current density of 0.2 A g−1.
    The maximum energy and power densities recorded from the device were 588.0 mWh
    kg−1 and 1.1 kW kg−1 at 1.5 A g−1. The device exhibited a remarkable retention
    of Csp of 98.9 % over 10,000 continuous galvanostatic charge–discharge cycles
    highlighting an excellent performance. Electrochemical impedance spectroscopy
    analysis emphasizes material’s excellent structural integrity. This is attributed
    to the crystalline phases present in the matrix.
acknowledgement: This work was partly supported by the Institute of Information &
  Communications Technology Planning & Evaluation (IITP) grant funded by the Korea
  government (MSIT) (No.RS-2021-II210077) and Korea Institute of Energy Technology
  Evaluation and Planning (KETEP) grant funded by the Korea government (MOTIE)(RS-2024-00398346,
  ESS BigData-Based O&M and Asset Management Technical Manpower Training).
article_number: '137869'
article_processing_charge: No
article_type: original
author:
- first_name: Neelima
  full_name: Mahato, Neelima
  last_name: Mahato
- first_name: Saurabh
  full_name: Singh, Saurabh
  id: 12d625da-9cb3-11ed-9667-af09d37d3f0a
  last_name: Singh
  orcid: 0000-0003-2209-5269
- first_name: T. V.M.
  full_name: Sreekanth, T. V.M.
  last_name: Sreekanth
- first_name: Kisoo
  full_name: Yoo, Kisoo
  last_name: Yoo
- first_name: Jonghoon
  full_name: Kim, Jonghoon
  last_name: Kim
citation:
  ama: 'Mahato N, Singh S, Sreekanth TVM, Yoo K, Kim J. In-situ engineered highly-crystalline
    Polythiophene empowered electrochemical capacitor-II: Anomalous electrochemical
    charge storage behavior of Polythiophene-rGO composite. <i>Materials Letters</i>.
    2025;382. doi:<a href="https://doi.org/10.1016/j.matlet.2024.137869">10.1016/j.matlet.2024.137869</a>'
  apa: 'Mahato, N., Singh, S., Sreekanth, T. V. M., Yoo, K., &#38; Kim, J. (2025).
    In-situ engineered highly-crystalline Polythiophene empowered electrochemical
    capacitor-II: Anomalous electrochemical charge storage behavior of Polythiophene-rGO
    composite. <i>Materials Letters</i>. Elsevier. <a href="https://doi.org/10.1016/j.matlet.2024.137869">https://doi.org/10.1016/j.matlet.2024.137869</a>'
  chicago: 'Mahato, Neelima, Saurabh Singh, T. V.M. Sreekanth, Kisoo Yoo, and Jonghoon
    Kim. “In-Situ Engineered Highly-Crystalline Polythiophene Empowered Electrochemical
    Capacitor-II: Anomalous Electrochemical Charge Storage Behavior of Polythiophene-RGO
    Composite.” <i>Materials Letters</i>. Elsevier, 2025. <a href="https://doi.org/10.1016/j.matlet.2024.137869">https://doi.org/10.1016/j.matlet.2024.137869</a>.'
  ieee: 'N. Mahato, S. Singh, T. V. M. Sreekanth, K. Yoo, and J. Kim, “In-situ engineered
    highly-crystalline Polythiophene empowered electrochemical capacitor-II: Anomalous
    electrochemical charge storage behavior of Polythiophene-rGO composite,” <i>Materials
    Letters</i>, vol. 382. Elsevier, 2025.'
  ista: 'Mahato N, Singh S, Sreekanth TVM, Yoo K, Kim J. 2025. In-situ engineered
    highly-crystalline Polythiophene empowered electrochemical capacitor-II: Anomalous
    electrochemical charge storage behavior of Polythiophene-rGO composite. Materials
    Letters. 382, 137869.'
  mla: 'Mahato, Neelima, et al. “In-Situ Engineered Highly-Crystalline Polythiophene
    Empowered Electrochemical Capacitor-II: Anomalous Electrochemical Charge Storage
    Behavior of Polythiophene-RGO Composite.” <i>Materials Letters</i>, vol. 382,
    137869, Elsevier, 2025, doi:<a href="https://doi.org/10.1016/j.matlet.2024.137869">10.1016/j.matlet.2024.137869</a>.'
  short: N. Mahato, S. Singh, T.V.M. Sreekanth, K. Yoo, J. Kim, Materials Letters
    382 (2025).
das_tickbox: '1'
dataavailabilitystatement: Data will be made available on request.
date_created: 2024-12-22T23:01:47Z
date_published: 2025-03-01T00:00:00Z
date_updated: 2026-10-16T10:00:45Z
day: '01'
department:
- _id: MaIb
doi: 10.1016/j.matlet.2024.137869
external_id:
  isi:
  - '001433664000001'
fulldoi: https://doi.org/10.1016/j.matlet.2024.137869
intvolume: '       382'
isi: 1
language:
- iso: eng
month: '03'
oa_version: None
publication: Materials Letters
publication_identifier:
  eissn:
  - 1873-4979
  issn:
  - 0167-577X
publication_status: published
publisher: Elsevier
quality_controlled: '1'
researchdata_availability: upon request
scopus_import: '1'
status: public
supplementarymaterial: yes
title: 'In-situ engineered highly-crystalline Polythiophene empowered electrochemical
  capacitor-II: Anomalous electrochemical charge storage behavior of Polythiophene-rGO
  composite'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 382
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
_id: '18753'
abstract:
- lang: eng
  text: "We continue a line of research which studies which hereditary families of
    digraphs have bounded dichromatic number. For a class of digraphs  C, a hero in
    \ C  is any digraph  H\r\n  such that  H -free digraphs in  C  have bounded dichromatic
    number. We show that if  F\r\n  is an oriented star of degree at least five, the
    only heroes for the class of  F -free digraphs are transitive tournaments. For
    oriented stars  F  of degree exactly four, we show the only heroes in  F -free
    digraphs are transitive tournaments, or possibly special joins of transitive tournaments.
    Aboulker et al. characterized the set of heroes of  {H,K1+P2→} -free digraphs
    almost completely, and we show the same characterization for the class of  {H,rK1+P3→}
    -free digraphs. Lastly, we show that if we forbid two \"valid\" orientations of
    brooms, then every transitive tournament is a hero for this class of digraphs."
acknowledgement: "We thank the anonymous referees for their careful proofreading which
  helped improve the presentation of this paper. We also thank one of the anonymous
  referees for pointing out our construction implies Theorem 1.7!\r\nBenjamin Moore
  finished this project while a postdoctoral researcher at Charles University, and
  was supported by project 22-17398S (Flows and cycles in graphs on surfaces) of the
  Czech Science Foundation. Benjamin Moore is currently funded by RANDSTRUCT No. 101076777,
  and appreciates the gracious support. We acknowledge the support of the Natural
  Sciences and Engineering Research Council of Canada (NSERC), [funding reference
  number RGPIN-2020-03912]. Cette recherche a été financée par le Conseil de recherches
  en sciences naturelles et en génie du Canada (CRSNG), [numéro de référence RGPIN-2020-03912].
  This project was funded in part by the Government of Ontario ."
article_number: '104104'
article_processing_charge: Yes (in subscription journal)
article_type: original
arxiv: 1
author:
- first_name: Alvaro
  full_name: Carbonero, Alvaro
  last_name: Carbonero
- first_name: Hidde
  full_name: Koerts, Hidde
  last_name: Koerts
- first_name: Benjamin
  full_name: Moore, Benjamin
  id: 6dc1a1be-bf1c-11ed-8d2b-d044840f49d6
  last_name: Moore
- first_name: Sophie
  full_name: Spirkl, Sophie
  last_name: Spirkl
citation:
  ama: Carbonero A, Koerts H, Moore B, Spirkl S. On heroes in digraphs with forbidden
    induced forests. <i>European Journal of Combinatorics</i>. 2025;125. doi:<a href="https://doi.org/10.1016/j.ejc.2024.104104">10.1016/j.ejc.2024.104104</a>
  apa: Carbonero, A., Koerts, H., Moore, B., &#38; Spirkl, S. (2025). On heroes in
    digraphs with forbidden induced forests. <i>European Journal of Combinatorics</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.ejc.2024.104104">https://doi.org/10.1016/j.ejc.2024.104104</a>
  chicago: Carbonero, Alvaro, Hidde Koerts, Benjamin Moore, and Sophie Spirkl. “On
    Heroes in Digraphs with Forbidden Induced Forests.” <i>European Journal of Combinatorics</i>.
    Elsevier, 2025. <a href="https://doi.org/10.1016/j.ejc.2024.104104">https://doi.org/10.1016/j.ejc.2024.104104</a>.
  ieee: A. Carbonero, H. Koerts, B. Moore, and S. Spirkl, “On heroes in digraphs with
    forbidden induced forests,” <i>European Journal of Combinatorics</i>, vol. 125.
    Elsevier, 2025.
  ista: Carbonero A, Koerts H, Moore B, Spirkl S. 2025. On heroes in digraphs with
    forbidden induced forests. European Journal of Combinatorics. 125, 104104.
  mla: Carbonero, Alvaro, et al. “On Heroes in Digraphs with Forbidden Induced Forests.”
    <i>European Journal of Combinatorics</i>, vol. 125, 104104, Elsevier, 2025, doi:<a
    href="https://doi.org/10.1016/j.ejc.2024.104104">10.1016/j.ejc.2024.104104</a>.
  short: A. Carbonero, H. Koerts, B. Moore, S. Spirkl, European Journal of Combinatorics
    125 (2025).
corr_author: '1'
das_tickbox: '0'
date_created: 2025-01-05T23:01:55Z
date_published: 2025-03-01T00:00:00Z
date_updated: 2026-10-16T10:13:50Z
day: '01'
ddc:
- '510'
department:
- _id: MaKw
doi: 10.1016/j.ejc.2024.104104
external_id:
  arxiv:
  - '2306.04710'
  isi:
  - '001400113700001'
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  date_created: 2025-04-16T09:16:25Z
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  file_size: 1110657
  relation: main_file
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file_date_updated: 2025-04-16T09:16:25Z
fulldoi: https://doi.org/10.1016/j.ejc.2024.104104
has_accepted_license: '1'
intvolume: '       125'
isi: 1
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
project:
- _id: bd95085b-d553-11ed-ba76-e55d3349be45
  grant_number: '101076777'
  name: Randomness and structure in combinatorics
publication: European Journal of Combinatorics
publication_identifier:
  issn:
  - 0195-6698
publication_status: published
publisher: Elsevier
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: no
title: On heroes in digraphs with forbidden induced forests
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 125
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
_id: '19603'
abstract:
- lang: eng
  text: "MaxCut is a classical NP-complete problem and a crucial building block in
    many\r\ncombinatorial algorithms. The famousEdwards-Erdös bound states that any
    connected\r\ngraph on n vertices with m edges contains a cut of size at least
    m/2 + n−1/4 . Crowston,\r\nJones and Mnich [Algorithmica, 2015] showed that the
    MaxCut problem on simple\r\nconnected graphs admits an FPT algorithm, where the
    parameter k is the difference\r\nbetween the desired cut size c and the lower
    bound given by the Edwards-Erdös\r\nbound. This was later improved by Etscheid
    and Mnich [Algorithmica, 2017] to run\r\nin parameterized linear time, i.e., f
    (k) · O(m). We improve upon this result in two\r\nways: Firstly, we extend the
    algorithm to work also for multigraphs (alternatively,\r\ngraphs with positive
    integer weights). Secondly, we change the parameter; instead of\r\nthe difference
    to the Edwards-Erdös bound, we use the difference to the Poljak-Turzík\r\nbound.
    The Poljak-Turzík bound states that any weighted graph G has a cut of weight\r\nat
    least w(G)/2 + wMSF (G)/4 , where w(G) denotes the total weight of G, and wMSF
    (G)\r\ndenotes the weight of its minimum spanning forest. In connected simple
    graphs the\r\ntwo bounds are equivalent, but for multigraphs the Poljak-Turzík
    bound can be larger\r\nand thus yield a smaller parameter k. Our algorithm also
    runs in parameterized linear\r\ntime, i.e., f (k) · O(m + n)."
acknowledgement: "Kalina Petrova is supported by the Swiss National Science Foundation,
  grant no. CRSII5 173721, and also receives funding from the European Union’s Horizon
  2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement
  No 101034413. Simon Weber is supported by the Swiss National Science Foundation
  under project no. 204320.\r\nOpen access funding provided by Swiss Federal Institute
  of Technology Zurich."
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Jonas
  full_name: Lill, Jonas
  last_name: Lill
- first_name: Kalina H
  full_name: Petrova, Kalina H
  id: 554ff4e4-f325-11ee-b0c4-a10dbd523381
  last_name: Petrova
- first_name: Simon
  full_name: Weber, Simon
  last_name: Weber
citation:
  ama: Lill J, Petrova KH, Weber S. Linear-time MaxCut in multigraphs parameterized
    above the Poljak-Turzík bound. <i>Algorithmica</i>. 2025;87:983-1007. doi:<a href="https://doi.org/10.1007/s00453-025-01306-y">10.1007/s00453-025-01306-y</a>
  apa: Lill, J., Petrova, K. H., &#38; Weber, S. (2025). Linear-time MaxCut in multigraphs
    parameterized above the Poljak-Turzík bound. <i>Algorithmica</i>. Springer Nature.
    <a href="https://doi.org/10.1007/s00453-025-01306-y">https://doi.org/10.1007/s00453-025-01306-y</a>
  chicago: Lill, Jonas, Kalina H Petrova, and Simon Weber. “Linear-Time MaxCut in
    Multigraphs Parameterized above the Poljak-Turzík Bound.” <i>Algorithmica</i>.
    Springer Nature, 2025. <a href="https://doi.org/10.1007/s00453-025-01306-y">https://doi.org/10.1007/s00453-025-01306-y</a>.
  ieee: J. Lill, K. H. Petrova, and S. Weber, “Linear-time MaxCut in multigraphs parameterized
    above the Poljak-Turzík bound,” <i>Algorithmica</i>, vol. 87. Springer Nature,
    pp. 983–1007, 2025.
  ista: Lill J, Petrova KH, Weber S. 2025. Linear-time MaxCut in multigraphs parameterized
    above the Poljak-Turzík bound. Algorithmica. 87, 983–1007.
  mla: Lill, Jonas, et al. “Linear-Time MaxCut in Multigraphs Parameterized above
    the Poljak-Turzík Bound.” <i>Algorithmica</i>, vol. 87, Springer Nature, 2025,
    pp. 983–1007, doi:<a href="https://doi.org/10.1007/s00453-025-01306-y">10.1007/s00453-025-01306-y</a>.
  short: J. Lill, K.H. Petrova, S. Weber, Algorithmica 87 (2025) 983–1007.
date_created: 2025-04-20T22:01:28Z
date_published: 2025-07-01T00:00:00Z
date_updated: 2026-10-16T10:13:33Z
day: '01'
ddc:
- '510'
department:
- _id: MaKw
doi: 10.1007/s00453-025-01306-y
ec_funded: 1
external_id:
  isi:
  - '001463103800001'
file:
- access_level: open_access
  checksum: eab3f1834b0ba347b05ae9897729c0ad
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  creator: dernst
  date_created: 2026-01-05T13:45:57Z
  date_updated: 2026-01-05T13:45:57Z
  file_id: '20957'
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  file_size: 448554
  relation: main_file
  success: 1
file_date_updated: 2026-01-05T13:45:57Z
fulldoi: https://doi.org/10.1007/s00453-025-01306-y
has_accepted_license: '1'
intvolume: '        87'
isi: 1
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 983-1007
project:
- _id: fc2ed2f7-9c52-11eb-aca3-c01059dda49c
  call_identifier: H2020
  grant_number: '101034413'
  name: 'IST-BRIDGE: International postdoctoral program'
publication: Algorithmica
publication_identifier:
  eissn:
  - 1432-0541
  issn:
  - 0178-4617
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  record:
  - id: '18758'
    relation: earlier_version
    status: public
scopus_import: '1'
status: public
title: Linear-time MaxCut in multigraphs parameterized above the Poljak-Turzík bound
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 87
year: '2025'
...
---
OA_place: publisher
_id: '20741'
abstract:
- lang: eng
  text: "Life on Earth emerged when biomacromolecules were membrane-enclosed in a
    confined space where many essential chemical reactions were more likely to happen
    and thereby accelerate evolution. These kinds of membranes separated internal
    reactions from the outside chaos while staying flexible so that those primordial
    cells can move, adopt their shape and, most importantly, propagate. Such membrane
    plasticity still remains a defining feature of all modern cell types. This remarkable
    ability to change their shape is most prominently observed during their propagation
    (i.e., cell division). Throughout division, a cell undergoes drastic change in
    its shape, usually at the middle of the cell, pulling the two opposite membrane
    sides inward, closer to each other, and, finally, culminating in pinching off
    to separate the cell into two daughter cells. To achieve this, a cell needs to
    employ a protein machinery, usually termed divisome, that can coordinate all necessary
    intracellular processes with membrane remodelling and synthesis of other extracellular
    structures that decorate a cell. The focus of this dissertation is a membrane-remodelling
    FtsZ system that is present across all domains of life. FtsZ forms filaments that
    further self-organize into ring-like structures at the cell septum and together
    with other division proteins perform cell envelope synthesis and constriction.
    However, there are still knowledge gaps in our mechanistic understanding of division
    in both archaea and bacteria. My work presented in this dissertation centres around
    a simple yet not well understood question: How is the divisome positioned correctly
    at the mid-cell? To achieve the proper positioning, the divisome needs to (i)
    be recruited to the mid-cell and (ii) localized orthogonally to the long cell
    axis. I tackle these processes in two different systems by applying an in vitro
    biochemical bottom-up reconstitution approach. I use purified components of Haloferax
    volcanii and Escherichia coli divisome to explore how divisome is recruited to
    the mid-cell in archaea and how the Z-ring positions orthogonally to the long
    cell axis in bacteria, respectively. \r\n\r\nFirstly, I collaborate with archaeal
    cell and structural biologists to explore the assembly of early division proteins
    in two FtsZ-containing archaeon H. volcanii, a standard model system for understudied
    archaeal organisms. I particularly address the hierarchy of interactions that
    allow a tripartite complex formation (SepF-CdpB1-CdpB2) and how the hierarchy
    of interactions ultimately leads to the recruitment of FtsZ filaments to the septum.
    This part of work has been published in (Nußbaum et al., 2024). In collaboration
    with evolutionary biologists, I shed light on ancient features that archaeal divisome
    has retained to this day and also speculate on a property that it might have lost
    during the course of evolution. \r\n\r\nNext, I switch my attention to E. coli
    divisome. Particularly, I address the FtsZ’s intrinsic biophysical property that
    drives the Z-ring diameter, and thereby the perpendicular orientation of the Z-ring
    to the long cell axis based on suggested membrane curvature sensing mechanism
    (Vanhille-Campos et al., 2024). This property allows formation of different Z-ring
    diameters that match the variety of cell diameters present in prokaryotes. The
    results showcase that the distribution of charged amino acids in the intrinsically
    disordered linker at the C-terminus (CTL) of FtsZ is the major determining factor
    of Z-ring diameter with inter-CTL interactions as an underlying mechanism. \r\n\r\nFinally,
    I thoroughly explain the methodology I used to address the abovementioned projects,
    and I finish with a discussion on how early archaeal divisome assembly and curvature
    sensing mechanism in bacteria, at first sight unrelated topics, are interconnected
    and important groundwork for both fundamental and translational research. "
acknowledged_ssus:
- _id: Bio
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Marko
  full_name: Kojic, Marko
  id: 73e7ecd4-dc85-11ea-9058-88a16394b160
  last_name: Kojic
  orcid: 0000-0001-7244-8128
citation:
  ama: Kojic M. Towards understanding the assembly mechanisms of the Z-ring in Archaea
    and Bacteria. 2025. doi:<a href="https://doi.org/10.15479/AT-ISTA-20741">10.15479/AT-ISTA-20741</a>
  apa: Kojic, M. (2025). <i>Towards understanding the assembly mechanisms of the Z-ring
    in Archaea and Bacteria</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT-ISTA-20741">https://doi.org/10.15479/AT-ISTA-20741</a>
  chicago: Kojic, Marko. “Towards Understanding the Assembly Mechanisms of the Z-Ring
    in Archaea and Bacteria.” Institute of Science and Technology Austria, 2025. <a
    href="https://doi.org/10.15479/AT-ISTA-20741">https://doi.org/10.15479/AT-ISTA-20741</a>.
  ieee: M. Kojic, “Towards understanding the assembly mechanisms of the Z-ring in
    Archaea and Bacteria,” Institute of Science and Technology Austria, 2025.
  ista: Kojic M. 2025. Towards understanding the assembly mechanisms of the Z-ring
    in Archaea and Bacteria. Institute of Science and Technology Austria.
  mla: Kojic, Marko. <i>Towards Understanding the Assembly Mechanisms of the Z-Ring
    in Archaea and Bacteria</i>. Institute of Science and Technology Austria, 2025,
    doi:<a href="https://doi.org/10.15479/AT-ISTA-20741">10.15479/AT-ISTA-20741</a>.
  short: M. Kojic, Towards Understanding the Assembly Mechanisms of the Z-Ring in
    Archaea and Bacteria, Institute of Science and Technology Austria, 2025.
corr_author: '1'
date_created: 2025-12-09T13:08:11Z
date_published: 2025-12-09T00:00:00Z
date_updated: 2026-10-16T10:35:47Z
day: '09'
ddc:
- '572'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MaLo
doi: 10.15479/AT-ISTA-20741
file:
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fulldoi: https://doi.org/10.15479/AT-ISTA-20741
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language:
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month: '12'
oa: 1
oa_version: Published Version
publication_identifier:
  isbn:
  - 978-3-99078-073-2
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '15118'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
title: Towards understanding the assembly mechanisms of the Z-ring in Archaea and
  Bacteria
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2025'
...
---
OA_place: publisher
OA_type: gold
_id: '19393'
abstract:
- lang: eng
  text: "Rotations constitute one of the fundamental symmetries in physics, characterized
    by their intricate group structure and infinite dimensional representations. In
    contrast to classical rotations, quantum mechanics unveils the SO(3) symmetry
    group structure, manifesting in phenomena without classical counterparts, from
    angular momentum quantization to non-trivial addition of angular momenta.\r\nWhile
    most studies of topological physics have focused on two-band systems, the SO(3)
    symmetry group of quantum rotors offers an inherently more complex platform with
    unprecedented possibilities for exploring topological phenomena. Despite their
    ubiquity in nature– from molecules to nanorotors– their potential for hosting
    topological phases has remained largely unexamined.\r\nIn this thesis, we mainly
    focus on periodically driven linear molecules as a prototype for studying topological
    phenomena in quantum rotors. Recent technological advances in coherent control
    of molecules, particularly through precisely shaped laser pulses, have made it
    possible to investigate linear rotors in the context of topology. While planar
    rotors have received some attention in recent years, threedimensional rotors–particularly
    linear molecules–harbor substantially richer topological phenomena due to their
    non-abelian nature and their additional angular degrees of freedom. We demonstrate
    that these systems can host novel edge states and topological features fundamentally
    impossible in planar systems.\r\nWe begin by establishing a theoretical bridge
    between periodically kicked rotors and \"crystalline\" lattices in angular momentum
    space. Using non-interacting linear molecules as our primary example, we show
    how quantum interference and revival patterns lead to the possibility to simulate
    band models with arbitrary number of bands N. While our framework applies to various
    quantum rotors, including nanorotors and kicked Bose-Einstein condensates, linear\r\nmolecules
    provide an ideal experimental platform due to their abovementioned precise controllability.\r\nThe
    core of this work examines adiabatic dynamics of 3D quantum rotors, establishing
    a geometric framework based on the Euler class to characterize its non-abelian
    topology. The non-Hermitian nature of the system enables novel braiding behaviors
    and topological transitions impossible in static systems, leading to an anomalous
    Dirac string phase with edge states in each gap, even though the Berry phases
    are all zero. These features can be directly observed through\r\nmolecular alignment
    and rotational level populations.\r\nThese findings establish quantum rotors as
    an alternative platform for studying multi-band topological physics, while suggesting
    practical implementations for quantum computation where topological protection
    could offer natural resilience against decoherence. The rich structure of three-dimensional
    rotation groups, combined with the tunability of topological features through
    driving parameters, makes this platform particularly valuable for exploring fundamental\r\nphysics
    and developing quantum technologies."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Volker
  full_name: Karle, Volker
  id: D7C012AE-D7ED-11E9-95E8-1EC5E5697425
  last_name: Karle
  orcid: 0000-0002-6963-0129
citation:
  ama: Karle V. Non-equilibrium topological phases with periodically driven molecules
    and quantum rotors. 2025. doi:<a href="https://doi.org/10.15479/AT-ISTA-19393">10.15479/AT-ISTA-19393</a>
  apa: Karle, V. (2025). <i>Non-equilibrium topological phases with periodically driven
    molecules and quantum rotors</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/AT-ISTA-19393">https://doi.org/10.15479/AT-ISTA-19393</a>
  chicago: Karle, Volker. “Non-Equilibrium Topological Phases with Periodically Driven
    Molecules and Quantum Rotors.” Institute of Science and Technology Austria, 2025.
    <a href="https://doi.org/10.15479/AT-ISTA-19393">https://doi.org/10.15479/AT-ISTA-19393</a>.
  ieee: V. Karle, “Non-equilibrium topological phases with periodically driven molecules
    and quantum rotors,” Institute of Science and Technology Austria, 2025.
  ista: Karle V. 2025. Non-equilibrium topological phases with periodically driven
    molecules and quantum rotors. Institute of Science and Technology Austria.
  mla: Karle, Volker. <i>Non-Equilibrium Topological Phases with Periodically Driven
    Molecules and Quantum Rotors</i>. Institute of Science and Technology Austria,
    2025, doi:<a href="https://doi.org/10.15479/AT-ISTA-19393">10.15479/AT-ISTA-19393</a>.
  short: V. Karle, Non-Equilibrium Topological Phases with Periodically Driven Molecules
    and Quantum Rotors, Institute of Science and Technology Austria, 2025.
corr_author: '1'
date_created: 2025-03-12T13:04:59Z
date_published: 2025-03-13T00:00:00Z
date_updated: 2026-10-16T12:16:52Z
day: '13'
ddc:
- '530'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MiLe
doi: 10.15479/AT-ISTA-19393
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  file_id: '19394'
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  file_size: 10625143
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  file_id: '19400'
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fulldoi: https://doi.org/10.15479/AT-ISTA-19393
has_accepted_license: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '03'
oa: 1
oa_version: Published Version
page: '192'
publication_identifier:
  eissn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '12788'
    relation: part_of_dissertation
    status: public
  - id: '9903'
    relation: part_of_dissertation
    status: public
  - id: '19425'
    relation: part_of_dissertation
    status: public
  - id: '14851'
    relation: part_of_dissertation
    status: public
  - id: '15004'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Mikhail
  full_name: Lemeshko, Mikhail
  id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
  last_name: Lemeshko
  orcid: 0000-0002-6990-7802
title: Non-equilibrium topological phases with periodically driven molecules and quantum
  rotors
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
_id: '18879'
abstract:
- lang: eng
  text: 'Our brain has remarkable computational power, generating sophisticated behaviors,
    storing memories over an individual’s lifetime, and producing higher cognitive
    functions. However, little of our neuroscience knowledge covers the human brain.
    Is this organ truly unique, or is it a scaled version of the extensively studied
    rodent brain? Combining multicellular patch-clamp recording with expansion-based
    superresolution microscopy and full-scale modeling, we determined the cellular
    and microcircuit properties of the human hippocampal CA3 region, a fundamental
    circuit for memory storage. In contrast to neocortical networks, human hippocampal
    CA3 displayed sparse connectivity, providing a circuit architecture that maximizes
    associational power. Human synapses showed unique reliability, high precision,
    and long integration times, exhibiting both species- and circuit-specific properties.
    Together with expanded neuronal numbers, these circuit characteristics greatly
    enhanced the memory storage capacity of CA3. Our results reveal distinct microcircuit
    properties of the human hippocampus and begin to unravel the inner workings of
    our most complex organ. '
acknowledged_ssus:
- _id: Bio
- _id: PreCl
- _id: LifeSc
- _id: M-Shop
- _id: ScienComp
acknowledgement: We thank Florian Marr for excellent technical assistance, Christina
  Altmutter and Julia Flor for technical support, Alois Schlögl for programming, Todor
  Asenov for development of the transportation box for human brain tissue, Tim Vogels
  for guidance on simulations, Marcus Huber for mathematical advice, Walter Kaufmann
  for assistance with handling frozen tissue, and Eleftheria Kralli-Beller for manuscript
  editing. This research was supported by the Scientific Services Units (SSUs) of
  ISTA, and we are grateful for assistance from Christoph Sommer and the Imaging and
  Optics Facility, Preclinical Facility, Lab Support Facility, Miba Machine Shop,
  and Scientific Computing. We are particularly grateful to the patient donors for
  their support of this project and also acknowledge the excellent support of the
  Medical University of Vienna Department of Neurosurgery staff; Romana Hoeftberger
  and the Division of Neuropathology and Neurochemistry; Gregor Kasprian and the Division
  of Neuroradiology and Musculoskeletal Radiology; and Christoph Baumgartner, Martha
  Feucht, and Ekaterina Pataraia for their clinical care of the patients included
  in this study. We thank Laura Jonkman, the NABCA biobank, and postmortem brain sample
  donors for their support of this research. The project received funding from the
  European Research Council (ERC) under the European Union’s Horizon 2020 research
  and innovation programme (advanced grant no. 692692 to P.J. and Marie Skłodowska-Curie
  Actions Individual Fellowship no. 101026635 to J.F.W.), the Austrian Science Fund
  (FWF; grant PAT 4178023 to P.J. and grant DK W1232 to M.R.T. and J.G.D.), the Austrian
  Academy of Sciences (DOC fellowship 26137 to M.R.T.), and a NOMIS-ISTA fellowship
  (to A.N.-O.).
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Jake
  full_name: Watson, Jake
  id: 63836096-4690-11EA-BD4E-32803DDC885E
  last_name: Watson
  orcid: 0000-0002-8698-3823
- first_name: Victor M
  full_name: Vargas Barroso, Victor M
  id: 2F55A9DE-F248-11E8-B48F-1D18A9856A87
  last_name: Vargas Barroso
- first_name: Rebecca
  full_name: Morse, Rebecca
  id: ceb89ae7-dc8d-11ea-abe3-da3301d0eab4
  last_name: Morse
- first_name: Andrea C
  full_name: Navas Olivé, Andrea C
  id: 739d26c9-52e8-11ee-8d72-f14d3893b4ce
  last_name: Navas Olivé
  orcid: 0000-0002-9280-8597
- first_name: Mojtaba
  full_name: Tavakoli, Mojtaba
  id: 3A0A06F4-F248-11E8-B48F-1D18A9856A87
  last_name: Tavakoli
  orcid: 0000-0002-7667-6854
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
- first_name: Matthias
  full_name: Tomschik, Matthias
  last_name: Tomschik
- first_name: Karl
  full_name: Rössler, Karl
  last_name: Rössler
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Watson J, Vargas Barroso VM, Morse R, et al. Human hippocampal CA3 uses specific
    functional connectivity rules for efficient associative memory. <i>Cell</i>. 2025;188(2):501-514.e18.
    doi:<a href="https://doi.org/10.1016/j.cell.2024.11.022">10.1016/j.cell.2024.11.022</a>
  apa: Watson, J., Vargas Barroso, V. M., Morse, R., Navas Olivé, A. C., Tavakoli,
    M., Danzl, J. G., … Jonas, P. M. (2025). Human hippocampal CA3 uses specific functional
    connectivity rules for efficient associative memory. <i>Cell</i>. Cell Press.
    <a href="https://doi.org/10.1016/j.cell.2024.11.022">https://doi.org/10.1016/j.cell.2024.11.022</a>
  chicago: Watson, Jake, Victor M Vargas Barroso, Rebecca Morse, Andrea C Navas Olivé,
    Mojtaba Tavakoli, Johann G Danzl, Matthias Tomschik, Karl Rössler, and Peter M
    Jonas. “Human Hippocampal CA3 Uses Specific Functional Connectivity Rules for
    Efficient Associative Memory.” <i>Cell</i>. Cell Press, 2025. <a href="https://doi.org/10.1016/j.cell.2024.11.022">https://doi.org/10.1016/j.cell.2024.11.022</a>.
  ieee: J. Watson <i>et al.</i>, “Human hippocampal CA3 uses specific functional connectivity
    rules for efficient associative memory,” <i>Cell</i>, vol. 188, no. 2. Cell Press,
    p. 501–514.e18, 2025.
  ista: Watson J, Vargas Barroso VM, Morse R, Navas Olivé AC, Tavakoli M, Danzl JG,
    Tomschik M, Rössler K, Jonas PM. 2025. Human hippocampal CA3 uses specific functional
    connectivity rules for efficient associative memory. Cell. 188(2), 501–514.e18.
  mla: Watson, Jake, et al. “Human Hippocampal CA3 Uses Specific Functional Connectivity
    Rules for Efficient Associative Memory.” <i>Cell</i>, vol. 188, no. 2, Cell Press,
    2025, p. 501–514.e18, doi:<a href="https://doi.org/10.1016/j.cell.2024.11.022">10.1016/j.cell.2024.11.022</a>.
  short: J. Watson, V.M. Vargas Barroso, R. Morse, A.C. Navas Olivé, M. Tavakoli,
    J.G. Danzl, M. Tomschik, K. Rössler, P.M. Jonas, Cell 188 (2025) 501–514.e18.
corr_author: '1'
date_created: 2025-01-26T23:01:49Z
date_published: 2025-01-23T00:00:00Z
date_updated: 2026-10-20T08:20:04Z
day: '23'
ddc:
- '570'
department:
- _id: JoDa
- _id: PeJo
- _id: GradSch
doi: 10.1016/j.cell.2024.11.022
ec_funded: 1
external_id:
  isi:
  - '001408395600001'
  pmid:
  - '39667938'
file:
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  checksum: d5a818edc32d249cdf75e1bb5b70a4b7
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  creator: dernst
  date_created: 2025-01-27T08:46:33Z
  date_updated: 2025-01-27T08:46:33Z
  file_id: '18884'
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  file_size: 14082343
  relation: main_file
  success: 1
file_date_updated: 2025-01-27T08:46:33Z
fulldoi: https://doi.org/10.1016/j.cell.2024.11.022
has_accepted_license: '1'
intvolume: '       188'
isi: 1
issue: '2'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 501-514.e18
pmid: 1
project:
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '692692'
  name: Biophysics and circuit function of a giant cortical glutamatergic synapse
- _id: fc2be41b-9c52-11eb-aca3-faa90aa144e9
  call_identifier: H2020
  grant_number: '101026635'
  name: Synaptic computations of the hippocampal CA3 circuitry
- _id: 6285a163-2b32-11ec-9570-8e204ca2dba5
  grant_number: '26137'
  name: Studying Organelle Structure and Function at Nanoscale Resolution with Expansion
    Microscopy
- _id: 2548AE96-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W1232
  name: Molecular Drug Targets
- _id: 8d9195e9-16d5-11f0-9cad-d075be887a1e
  grant_number: PAT 4178023
  name: Synaptic networks of human brain
- _id: 9B861AAC-BA93-11EA-9121-9846C619BF3A
  name: NOMIS Fellowship Program
publication: Cell
publication_identifier:
  eissn:
  - 1097-4172
  issn:
  - 0092-8674
publication_status: published
publisher: Cell Press
quality_controlled: '1'
related_material:
  record:
  - id: '18688'
    relation: earlier_version
    status: public
scopus_import: '1'
status: public
title: Human hippocampal CA3 uses specific functional connectivity rules for efficient
  associative memory
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 188
year: '2025'
...
---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '19404'
abstract:
- lang: eng
  text: Cell migration is a fundamental process during embryonic development. Most
    studies in vivo have focused on the migration of cells using the extracellular
    matrix (ECM) as their substrate for migration. In contrast, much less is known
    about how cells migrate on other cells, as found in early embryos when the ECM
    has not yet formed. Here, we show that lateral mesendoderm (LME) cells in the
    early zebrafish gastrula use the ectoderm as their substrate for migration. We
    show that the lateral ectoderm is permissive for the animal-pole-directed migration
    of LME cells, while the ectoderm at the animal pole halts it. These differences
    in permissiveness depend on the lateral ectoderm being more cohesive than the
    animal ectoderm, a property controlled by bone morphogenetic protein (BMP) signaling
    within the ectoderm. Collectively, these findings identify ectoderm tissue cohesion
    as one critical factor in regulating LME migration during zebrafish gastrulation.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: ScienComp
acknowledgement: 'We are grateful to the colleagues who contributed to this work with
  discussions, technical advice, and feedback on the manuscript: Irene Steccari, David
  Labrousse Arias and the other members of the Heisenberg lab, Nicole Amberg, Florian
  Pauler, Nicoletta Petridou, Elena Scarpa, and Edouard Hannezo. We also thank the
  Imaging and Optics Facility, the Life Science Facility, and the Scientific Computing
  Unit at ISTA for support. The Next Generation Sequencing Facility at Vienna BioCenter
  Core Facilities performed the RNA-seq for animal and lateral ectoderm. D.B.B. was
  supported by the NOMIS Foundation as a NOMIS Fellow and by an EMBO Postdoctoral
  Fellowship (ALTF 343-2022). S. Tavano was supported by an EMBO Postdoctoral Fellowship
  (ALTF 1159-2018).'
article_number: '115387'
article_processing_charge: Yes
article_type: original
author:
- first_name: Ste
  full_name: Tavano, Ste
  id: 2F162F0C-F248-11E8-B48F-1D18A9856A87
  last_name: Tavano
  orcid: 0000-0001-9970-7804
- first_name: David
  full_name: Brückner, David
  id: e1e86031-6537-11eb-953a-f7ab92be508d
  last_name: Brückner
  orcid: 0000-0001-7205-2975
- first_name: Saren
  full_name: Tasciyan, Saren
  id: 4323B49C-F248-11E8-B48F-1D18A9856A87
  last_name: Tasciyan
  orcid: 0000-0003-1671-393X
- first_name: Xin
  full_name: Tong, Xin
  id: 50F65CDC-AA30-11E9-A72B-8A12E6697425
  last_name: Tong
- first_name: Roland
  full_name: Kardos, Roland
  id: 4039350E-F248-11E8-B48F-1D18A9856A87
  last_name: Kardos
- first_name: Alexandra
  full_name: Schauer, Alexandra
  id: 30A536BA-F248-11E8-B48F-1D18A9856A87
  last_name: Schauer
  orcid: 0000-0001-7659-9142
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
citation:
  ama: Tavano S, Brückner D, Tasciyan S, et al. BMP-dependent patterning of ectoderm
    tissue material properties modulates lateral mesendoderm cell migration during
    early zebrafish gastrulation. <i>Cell Reports</i>. 2025;44(3). doi:<a href="https://doi.org/10.1016/j.celrep.2025.115387">10.1016/j.celrep.2025.115387</a>
  apa: Tavano, S., Brückner, D., Tasciyan, S., Tong, X., Kardos, R., Schauer, A.,
    … Heisenberg, C.-P. J. (2025). BMP-dependent patterning of ectoderm tissue material
    properties modulates lateral mesendoderm cell migration during early zebrafish
    gastrulation. <i>Cell Reports</i>. Cell Press. <a href="https://doi.org/10.1016/j.celrep.2025.115387">https://doi.org/10.1016/j.celrep.2025.115387</a>
  chicago: Tavano, Ste, David Brückner, Saren Tasciyan, Xin Tong, Roland Kardos, Alexandra
    Schauer, Robert Hauschild, and Carl-Philipp J Heisenberg. “BMP-Dependent Patterning
    of Ectoderm Tissue Material Properties Modulates Lateral Mesendoderm Cell Migration
    during Early Zebrafish Gastrulation.” <i>Cell Reports</i>. Cell Press, 2025. <a
    href="https://doi.org/10.1016/j.celrep.2025.115387">https://doi.org/10.1016/j.celrep.2025.115387</a>.
  ieee: S. Tavano <i>et al.</i>, “BMP-dependent patterning of ectoderm tissue material
    properties modulates lateral mesendoderm cell migration during early zebrafish
    gastrulation,” <i>Cell Reports</i>, vol. 44, no. 3. Cell Press, 2025.
  ista: Tavano S, Brückner D, Tasciyan S, Tong X, Kardos R, Schauer A, Hauschild R,
    Heisenberg C-PJ. 2025. BMP-dependent patterning of ectoderm tissue material properties
    modulates lateral mesendoderm cell migration during early zebrafish gastrulation.
    Cell Reports. 44(3), 115387.
  mla: Tavano, Ste, et al. “BMP-Dependent Patterning of Ectoderm Tissue Material Properties
    Modulates Lateral Mesendoderm Cell Migration during Early Zebrafish Gastrulation.”
    <i>Cell Reports</i>, vol. 44, no. 3, 115387, Cell Press, 2025, doi:<a href="https://doi.org/10.1016/j.celrep.2025.115387">10.1016/j.celrep.2025.115387</a>.
  short: S. Tavano, D. Brückner, S. Tasciyan, X. Tong, R. Kardos, A. Schauer, R. Hauschild,
    C.-P.J. Heisenberg, Cell Reports 44 (2025).
corr_author: '1'
date_created: 2025-03-16T23:01:24Z
date_published: 2025-03-25T00:00:00Z
date_updated: 2026-10-20T08:20:45Z
day: '25'
ddc:
- '570'
department:
- _id: CaHe
- _id: EdHa
- _id: MiSi
- _id: Bio
doi: 10.1016/j.celrep.2025.115387
external_id:
  isi:
  - '001443652700001'
  pmid:
  - '40057955'
file:
- access_level: open_access
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  content_type: application/pdf
  creator: dernst
  date_created: 2025-03-17T10:26:54Z
  date_updated: 2025-03-17T10:26:54Z
  file_id: '19413'
  file_name: 2025_CellReports_Tavano.pdf
  file_size: 9067797
  relation: main_file
  success: 1
file_date_updated: 2025-03-17T10:26:54Z
fulldoi: https://doi.org/10.1016/j.celrep.2025.115387
has_accepted_license: '1'
intvolume: '        44'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 34e2a5b5-11ca-11ed-8bc3-b2265616ef0b
  grant_number: ALTF 343-2022
  name: A mechano-chemical theory for stem cell fate decisions in organoid development
- _id: 269CD5C4-B435-11E9-9278-68D0E5697425
  grant_number: ALTF 1159-2018
  name: 'Mechanosensation in cell migration: the role of friction forces in cell polarization
    and directed migration'
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
  issn:
  - 2639-1856
publication_status: published
publisher: Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: BMP-dependent patterning of ectoderm tissue material properties modulates lateral
  mesendoderm cell migration during early zebrafish gastrulation
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 44
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
PlanS_conform: '1'
_id: '19602'
abstract:
- lang: eng
  text: N4-methylcytosine (4mC) is an important DNA modification in prokaryotes, but
    its relevance and even its presence in eukaryotes have been mysterious. Here we
    show that spermatogenesis in the liverwort Marchantia polymorpha involves two
    waves of extensive DNA methylation reprogramming. First, 5-methylcytosine (5mC)
    expands from transposons to the entire genome. Notably, the second wave installs
    4mC throughout genic regions, covering over 50% of CG sites in sperm. 4mC requires
    a methyltransferase (MpDN4MT1a) that is specifically expressed during late spermiogenesis.
    Deletion of MpDN4MT1a alters the sperm transcriptome, causes sperm swimming and
    fertility defects, and impairs post-fertilization development. Our results reveal
    extensive 4mC in a eukaryote, identify a family of eukaryotic methyltransferases,
    and elucidate the biological functions of 4mC in reproductive development, thereby
    expanding the repertoire of functional eukaryotic DNA modifications.
acknowledged_ssus:
- _id: Bio
- _id: ScienComp
acknowledgement: We thank Sir Richard Roberts (NEB) for the kind gift of anti-4mC
  antibodies. We are also grateful to the JIC Small Molecule Mass Spectrometry (Lionel
  Hill) and Chemistry (Martin Rejzek) platforms as well as the High Resolution Metabolomics
  Laboratory (Manfred Beckmann, Aberystwyth University) for their assistance with
  LC-MS. Additionally, we acknowledge the assistance of the JIC Bioimaging Facility
  and ISTA Imaging and Optics Facility for microscopy. Finally, we appreciate the
  High Performance Computing resources provided by the ISTA Scientific Computing Facility
  and Norwich BioScience Institute Partnership Computing Infrastructure. This work
  was funded by a Sainsbury Charitable Foundation studentship (J.W.), a UKRI-BBSRC
  Doctoral Training Partnerships studentship (BBT0087171 to J.T.), a European Research
  Council Starting Grant (“SexMeth” 804981 to J.W., S.X., and X.F.), two Biotechnology
  and Biological Sciences Research Council (BBSRC) grants (BBS0096201 and BBP0135111
  to J.Z., M.V., and X.F.), an EMBO Long Term Fellowship (Y.L.), an ISTA Bridge Fellowship
  (S.X.), and ISTA core funding (Y.Y. and X.F.).
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: James
  full_name: Walker, James
  last_name: Walker
- first_name: Jingyi
  full_name: Zhang, Jingyi
  last_name: Zhang
- first_name: Yalin
  full_name: Liu, Yalin
  last_name: Liu
- first_name: Shujuan
  full_name: Xu, Shujuan
  id: 9724dd9d-f591-11ee-bd51-e97ed0652286
  last_name: Xu
- first_name: Yiming
  full_name: Yu, Yiming
  id: 318e643b-8b61-11ed-b69e-aafa103ec8dd
  last_name: Yu
  orcid: 0000-0002-9919-7282
- first_name: Martin
  full_name: Vickers, Martin
  last_name: Vickers
- first_name: Weizhi
  full_name: Ouyang, Weizhi
  id: fec73395-8b60-11ed-b69e-927fda99c743
  last_name: Ouyang
- first_name: Judit
  full_name: Tálas, Judit
  last_name: Tálas
- first_name: Liam
  full_name: Dolan, Liam
  last_name: Dolan
- first_name: Keiji
  full_name: Nakajima, Keiji
  last_name: Nakajima
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
citation:
  ama: Walker J, Zhang J, Liu Y, et al. Extensive N4 cytosine methylation is essential
    for Marchantia sperm function. <i>Cell</i>. 2025;188(11):2890-2906.e14. doi:<a
    href="https://doi.org/10.1016/j.cell.2025.03.014">10.1016/j.cell.2025.03.014</a>
  apa: Walker, J., Zhang, J., Liu, Y., Xu, S., Yu, Y., Vickers, M., … Feng, X. (2025).
    Extensive N4 cytosine methylation is essential for Marchantia sperm function.
    <i>Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.cell.2025.03.014">https://doi.org/10.1016/j.cell.2025.03.014</a>
  chicago: Walker, James, Jingyi Zhang, Yalin Liu, Shujuan Xu, Yiming Yu, Martin Vickers,
    Weizhi Ouyang, et al. “Extensive N4 Cytosine Methylation Is Essential for Marchantia
    Sperm Function.” <i>Cell</i>. Cell Press, 2025. <a href="https://doi.org/10.1016/j.cell.2025.03.014">https://doi.org/10.1016/j.cell.2025.03.014</a>.
  ieee: J. Walker <i>et al.</i>, “Extensive N4 cytosine methylation is essential for
    Marchantia sperm function,” <i>Cell</i>, vol. 188, no. 11. Cell Press, p. 2890–2906.e14,
    2025.
  ista: Walker J, Zhang J, Liu Y, Xu S, Yu Y, Vickers M, Ouyang W, Tálas J, Dolan
    L, Nakajima K, Feng X. 2025. Extensive N4 cytosine methylation is essential for
    Marchantia sperm function. Cell. 188(11), 2890–2906.e14.
  mla: Walker, James, et al. “Extensive N4 Cytosine Methylation Is Essential for Marchantia
    Sperm Function.” <i>Cell</i>, vol. 188, no. 11, Cell Press, 2025, p. 2890–2906.e14,
    doi:<a href="https://doi.org/10.1016/j.cell.2025.03.014">10.1016/j.cell.2025.03.014</a>.
  short: J. Walker, J. Zhang, Y. Liu, S. Xu, Y. Yu, M. Vickers, W. Ouyang, J. Tálas,
    L. Dolan, K. Nakajima, X. Feng, Cell 188 (2025) 2890–2906.e14.
corr_author: '1'
date_created: 2025-04-20T22:01:28Z
date_published: 2025-05-29T00:00:00Z
date_updated: 2026-10-20T08:22:21Z
day: '29'
ddc:
- '570'
department:
- _id: XiFe
doi: 10.1016/j.cell.2025.03.014
ec_funded: 1
external_id:
  isi:
  - '001504744800006'
  pmid:
  - '40209706'
file:
- access_level: open_access
  checksum: 0dcc2feb368dfe7c4890093366b2dacb
  content_type: application/pdf
  creator: dernst
  date_created: 2025-12-29T13:40:32Z
  date_updated: 2025-12-29T13:40:32Z
  file_id: '20871'
  file_name: 2025_Cell_Walker.pdf
  file_size: 11622960
  relation: main_file
  success: 1
file_date_updated: 2025-12-29T13:40:32Z
fulldoi: https://doi.org/10.1016/j.cell.2025.03.014
has_accepted_license: '1'
intvolume: '       188'
isi: 1
issue: '11'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 2890-2906.e14
pmid: 1
project:
- _id: bdb51a6e-d553-11ed-ba76-c2025f3d5725
  call_identifier: H2020
  grant_number: '804981'
  name: Establishment, modulation and inheritance of sexual lineage specific DNA methylation
    in plants
publication: Cell
publication_identifier:
  eissn:
  - 1097-4172
  issn:
  - 0092-8674
publication_status: published
publisher: Cell Press
quality_controlled: '1'
related_material:
  link:
  - description: News on ISTA website
    relation: press_release
    url: https://ista.ac.at/en/news/from-bacterial-immunity-to-plant-sex/
scopus_import: '1'
status: public
title: Extensive N4 cytosine methylation is essential for Marchantia sperm function
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 188
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
PlanS_conform: '1'
_id: '19703'
abstract:
- lang: eng
  text: An enlarged brain underlies the complex central nervous system of vertebrates.
    The dramatic expansion of the brain that diverges its shape from the spinal cord
    follows neural tube closure during embryonic development. Here, we show that this
    differential deformation is encoded by a pre-pattern of tissue material properties
    in chicken embryos. Using magnetic droplets and atomic force microscopy, we demonstrate
    that the dorsal hindbrain is more fluid than the dorsal spinal cord, resulting
    in a thinning versus a resisting response to increasing lumen pressure, respectively.
    The dorsal hindbrain exhibits reduced apical actin and a disorganized laminin
    matrix consistent with tissue fluidization. Blocking the activity of neural-crest-associated
    matrix metalloproteinases inhibits hindbrain expansion. Transplanting dorsal hindbrain
    cells to the spinal cord can locally create an expanded brain-like morphology
    in some cases. Our findings raise questions in vertebrate head evolution and suggest
    a general role of mechanical pre-patterning in sculpting epithelial tubes.
acknowledgement: 'We thank A. Dimitracopoulos, K. Kawaguchi, J. Vidigueira, B. Baum,
  I. McLaren, D. St Johnston, and members of the Buckley, Scarpa, Steventon, Kawaguchi,
  and Xiong labs for technical assistance and constructive feedback. We thank Ryan
  Greenhalgh for methods developed to obtain fluidity values from AFM data. We thank
  Nicola Lawrence, Alex Sossick, and Sargon Gross-Thebing from the Gurdon Institute
  Imaging Facility for microscopy support. Funding: this work was supported by a Wellcome
  Trust/Royal Society Sir Henry Dale Fellowship (215439/Z/19/Z) and UKRI-EPSRC Frontier
  Research Grant (EP/X023761/1, originally selected as an ERC Starting Grant) to F.X.;
  an ERC Consolidator Grant (772426), ERC Synergy Grant 101118729 UNFOLD, and Alexander
  von Humboldt Professorship ( Alexander von Humboldt Foundation) to K.F.; and an
  ERC Starting Grant (851288) to E.H.'
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Susannah B.P.
  full_name: Mclaren, Susannah B.P.
  last_name: Mclaren
- first_name: Shi-lei
  full_name: Xue, Shi-lei
  id: 31D2C804-F248-11E8-B48F-1D18A9856A87
  last_name: Xue
- first_name: Siyuan
  full_name: Ding, Siyuan
  last_name: Ding
- first_name: Alexander K.
  full_name: Winkel, Alexander K.
  last_name: Winkel
- first_name: Oscar
  full_name: Baldwin, Oscar
  last_name: Baldwin
- first_name: Shreya
  full_name: Dwarakacherla, Shreya
  last_name: Dwarakacherla
- first_name: Kristian
  full_name: Franze, Kristian
  last_name: Franze
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
- first_name: Fengzhu
  full_name: Xiong, Fengzhu
  last_name: Xiong
citation:
  ama: Mclaren SBP, Xue S, Ding S, et al. Differential tissue deformability underlies
    fluid pressure-driven shape divergence of the avian embryonic brain and spinal
    cord. <i>Developmental Cell</i>. 2025;60(17):2237-2247.e4. doi:<a href="https://doi.org/10.1016/j.devcel.2025.04.010">10.1016/j.devcel.2025.04.010</a>
  apa: Mclaren, S. B. P., Xue, S., Ding, S., Winkel, A. K., Baldwin, O., Dwarakacherla,
    S., … Xiong, F. (2025). Differential tissue deformability underlies fluid pressure-driven
    shape divergence of the avian embryonic brain and spinal cord. <i>Developmental
    Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.devcel.2025.04.010">https://doi.org/10.1016/j.devcel.2025.04.010</a>
  chicago: Mclaren, Susannah B.P., Shi-lei Xue, Siyuan Ding, Alexander K. Winkel,
    Oscar Baldwin, Shreya Dwarakacherla, Kristian Franze, Edouard B Hannezo, and Fengzhu
    Xiong. “Differential Tissue Deformability Underlies Fluid Pressure-Driven Shape
    Divergence of the Avian Embryonic Brain and Spinal Cord.” <i>Developmental Cell</i>.
    Cell Press, 2025. <a href="https://doi.org/10.1016/j.devcel.2025.04.010">https://doi.org/10.1016/j.devcel.2025.04.010</a>.
  ieee: S. B. P. Mclaren <i>et al.</i>, “Differential tissue deformability underlies
    fluid pressure-driven shape divergence of the avian embryonic brain and spinal
    cord,” <i>Developmental Cell</i>, vol. 60, no. 17. Cell Press, p. 2237–2247.e4,
    2025.
  ista: Mclaren SBP, Xue S, Ding S, Winkel AK, Baldwin O, Dwarakacherla S, Franze
    K, Hannezo EB, Xiong F. 2025. Differential tissue deformability underlies fluid
    pressure-driven shape divergence of the avian embryonic brain and spinal cord.
    Developmental Cell. 60(17), 2237–2247.e4.
  mla: Mclaren, Susannah B. P., et al. “Differential Tissue Deformability Underlies
    Fluid Pressure-Driven Shape Divergence of the Avian Embryonic Brain and Spinal
    Cord.” <i>Developmental Cell</i>, vol. 60, no. 17, Cell Press, 2025, p. 2237–2247.e4,
    doi:<a href="https://doi.org/10.1016/j.devcel.2025.04.010">10.1016/j.devcel.2025.04.010</a>.
  short: S.B.P. Mclaren, S. Xue, S. Ding, A.K. Winkel, O. Baldwin, S. Dwarakacherla,
    K. Franze, E.B. Hannezo, F. Xiong, Developmental Cell 60 (2025) 2237–2247.e4.
date_created: 2025-05-18T22:02:50Z
date_published: 2025-09-08T00:00:00Z
date_updated: 2026-10-20T08:25:00Z
day: '08'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1016/j.devcel.2025.04.010
ec_funded: 1
external_id:
  isi:
  - '001570502100005'
  pmid:
  - '40347948'
file:
- access_level: open_access
  checksum: 1ca6f0822c1cbd430686d5e2a4f96401
  content_type: application/pdf
  creator: dernst
  date_created: 2025-12-29T13:45:05Z
  date_updated: 2025-12-29T13:45:05Z
  file_id: '20872'
  file_name: 2025_DevelopmentalCell_McLaren.pdf
  file_size: 12564806
  relation: main_file
  success: 1
file_date_updated: 2025-12-29T13:45:05Z
fulldoi: https://doi.org/10.1016/j.devcel.2025.04.010
has_accepted_license: '1'
intvolume: '        60'
isi: 1
issue: '17'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 2237-2247.e4
pmid: 1
project:
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
publication: Developmental Cell
publication_identifier:
  eissn:
  - 1878-1551
  issn:
  - 1534-5807
publication_status: published
publisher: Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Differential tissue deformability underlies fluid pressure-driven shape divergence
  of the avian embryonic brain and spinal cord
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 60
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
PlanS_conform: '1'
_id: '20143'
abstract:
- lang: eng
  text: Bacteria and archaea deploy diverse antiviral defense systems, many of which
    remain mechanistically uncharacterized. Here, we characterize Kiwa, a widespread
    two-component system composed of the transmembrane sensor KwaA and the DNA-binding
    effector KwaB. Cryogenic electron microscopy (cryo-EM) analysis reveals that KwaA
    and KwaB assemble into a large, membrane-associated supercomplex. Upon phage binding,
    KwaA senses infection at the membrane, leading to KwaB binding of ejected phage
    DNA and inhibition of replication and late transcription, without inducing host
    cell death. Although KwaB can bind DNA independently, its antiviral activity requires
    association with KwaA, suggesting spatial or conformational regulation. We show
    that the phage-encoded DNA-mimic protein Gam directly binds and inhibits KwaB
    but that co-expression with the Gam-targeted RecBCD system restores protection
    by Kiwa. Our findings support a model in which Kiwa coordinates membrane-associated
    detection of phage infection with downstream DNA binding by its effector, forming
    a spatially coordinated antiviral mechanism.
acknowledgement: We thank Rotem Sorek (Weizmann Institute of Science) for the Lambda
  Gam mutant and Ian Molineux (University of Texas) for T4Δgp2. We thank You Yu (Zhejiang
  University-University of Edinburgh Institute) and J. De La Cruz (MSK) for assistance
  with cryo-EM data collection and Lyuqin Zheng (MSK) for discussions on structural
  analysis. We thank the Imaging and Microscopy Centre (IMC) at the University of
  Southampton. This work was supported by Royal Society grant RGS\R2\222312 to F.L.N.;
  Welch Foundation grant F-1938 and National Institutes of Health R35GM138348 to D.W.T.;
  Wessex Medical Research Innovation grant AE06 to T.A.; and NIH grant GM145888 and
  Maloris Foundation and Memorial Sloan-Kettering Core grant (P30-CA008748) to D.J.P.
  In addition to MSKCC cryo-EM resources, some of this work was performed at the National
  Center for CryoEM Access and Training (NCCAT) and the Simons Electron Microscopy
  Center located at the New York Structural Biology Center, supported by the NIH Common
  Fund Transformative High Resolution Cryo-Electron Microscopy program (U24 GM129539)
  and Simons Foundation (SF349247) and NY State Assembly grants. This research used
  NSLS-II MX X-ray User Resources (FMX) of the National Synchrotron Light Source II,
  operated for the DOE Office of Science by Brookhaven National Laboratory under contract
  no. DE-SC0012704. The Center for BioMolecular Structure (CBMS) is primarily supported
  by the NIH, the National Institute of General Medical Sciences (NIGMS) through a
  Center Core P30 Grant (P30GM133893), and by the DOE Office of Biological and Environmental
  Research (KP1605010). R.K. and E.V.K. are supported by the Intramural Research Program
  of the NIH (National Library of Medicine).
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Zhiying
  full_name: Zhang, Zhiying
  last_name: Zhang
- first_name: Thomas C.
  full_name: Todeschini, Thomas C.
  last_name: Todeschini
- first_name: Yi
  full_name: Wu, Yi
  last_name: Wu
- first_name: Roman
  full_name: Kogay, Roman
  last_name: Kogay
- first_name: Ameena
  full_name: Naji, Ameena
  last_name: Naji
- first_name: Joaquin
  full_name: Cardenas Rodriguez, Joaquin
  last_name: Cardenas Rodriguez
- first_name: Rupavidhya
  full_name: Mondi, Rupavidhya
  last_name: Mondi
- first_name: Daniel
  full_name: Kaganovich, Daniel
  last_name: Kaganovich
- first_name: David W.
  full_name: Taylor, David W.
  last_name: Taylor
- first_name: Jack Peter Kelly
  full_name: Bravo, Jack Peter Kelly
  id: 96aecfa5-8931-11ee-af30-aa6a5d6eee0e
  last_name: Bravo
  orcid: 0000-0003-0456-0753
- first_name: Marianna
  full_name: Teplova, Marianna
  last_name: Teplova
- first_name: Triana
  full_name: Amen, Triana
  last_name: Amen
- first_name: Eugene
  full_name: Koonin, Eugene
  last_name: Koonin
- first_name: Dinshaw J.
  full_name: Patel, Dinshaw J.
  last_name: Patel
- first_name: Franklin L.
  full_name: Nobrega, Franklin L.
  last_name: Nobrega
citation:
  ama: Zhang Z, Todeschini TC, Wu Y, et al. Kiwa is a membrane-embedded defense supercomplex
    activated at phage attachment sites. <i>Cell</i>. 2025;188(21):5862-5877.e23.
    doi:<a href="https://doi.org/10.1016/j.cell.2025.07.002">10.1016/j.cell.2025.07.002</a>
  apa: Zhang, Z., Todeschini, T. C., Wu, Y., Kogay, R., Naji, A., Cardenas Rodriguez,
    J., … Nobrega, F. L. (2025). Kiwa is a membrane-embedded defense supercomplex
    activated at phage attachment sites. <i>Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.cell.2025.07.002">https://doi.org/10.1016/j.cell.2025.07.002</a>
  chicago: Zhang, Zhiying, Thomas C. Todeschini, Yi Wu, Roman Kogay, Ameena Naji,
    Joaquin Cardenas Rodriguez, Rupavidhya Mondi, et al. “Kiwa Is a Membrane-Embedded
    Defense Supercomplex Activated at Phage Attachment Sites.” <i>Cell</i>. Cell Press,
    2025. <a href="https://doi.org/10.1016/j.cell.2025.07.002">https://doi.org/10.1016/j.cell.2025.07.002</a>.
  ieee: Z. Zhang <i>et al.</i>, “Kiwa is a membrane-embedded defense supercomplex
    activated at phage attachment sites,” <i>Cell</i>, vol. 188, no. 21. Cell Press,
    p. 5862–5877.e23, 2025.
  ista: Zhang Z, Todeschini TC, Wu Y, Kogay R, Naji A, Cardenas Rodriguez J, Mondi
    R, Kaganovich D, Taylor DW, Bravo JPK, Teplova M, Amen T, Koonin E, Patel DJ,
    Nobrega FL. 2025. Kiwa is a membrane-embedded defense supercomplex activated at
    phage attachment sites. Cell. 188(21), 5862–5877.e23.
  mla: Zhang, Zhiying, et al. “Kiwa Is a Membrane-Embedded Defense Supercomplex Activated
    at Phage Attachment Sites.” <i>Cell</i>, vol. 188, no. 21, Cell Press, 2025, p.
    5862–5877.e23, doi:<a href="https://doi.org/10.1016/j.cell.2025.07.002">10.1016/j.cell.2025.07.002</a>.
  short: Z. Zhang, T.C. Todeschini, Y. Wu, R. Kogay, A. Naji, J. Cardenas Rodriguez,
    R. Mondi, D. Kaganovich, D.W. Taylor, J.P.K. Bravo, M. Teplova, T. Amen, E. Koonin,
    D.J. Patel, F.L. Nobrega, Cell 188 (2025) 5862–5877.e23.
date_created: 2025-08-07T05:00:04Z
date_published: 2025-10-16T00:00:00Z
date_updated: 2026-10-20T08:23:33Z
day: '16'
ddc:
- '570'
department:
- _id: JaBr
doi: 10.1016/j.cell.2025.07.002
external_id:
  isi:
  - '001603560700005'
  pmid:
  - '40730155'
file:
- access_level: open_access
  checksum: b944de5fbd7455f58e1ff338ad352239
  content_type: application/pdf
  creator: dernst
  date_created: 2025-12-29T14:15:25Z
  date_updated: 2025-12-29T14:15:25Z
  file_id: '20875'
  file_name: 2025_Cell_Zhang.pdf
  file_size: 32104588
  relation: main_file
  success: 1
file_date_updated: 2025-12-29T14:15:25Z
fulldoi: https://doi.org/10.1016/j.cell.2025.07.002
has_accepted_license: '1'
intvolume: '       188'
isi: 1
issue: '21'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 5862-5877.e23
pmid: 1
publication: Cell
publication_identifier:
  eissn:
  - 1097-4172
  issn:
  - 0092-8674
publication_status: published
publisher: Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Kiwa is a membrane-embedded defense supercomplex activated at phage attachment
  sites
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 188
year: '2025'
...
---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '19846'
abstract:
- lang: eng
  text: The Ca2+-release-activated Ca2+ (CRAC) channel Orai1 is activated by interaction
    with the Ca2+ sensor Stromal Interaction Molecule 1 (STIM1). Owing to the lack
    of structurally resolved Orai1/STIM1 complexes, the impact of their coupling on
    individual Orai1 transmembrane domain (TM) movements is unclear. This study investigates
    STIM1-independent and STIM1-dependent Orai1-TM dynamics using photocrosslinking
    unnatural amino acids (UAAs) at each individual TM position. We primarily identify
    CRAC-channel-like currents directly after UAA incorporation or additional UV-light
    irradiation at TM3 sites that interface with non-pore-lining TMs. Using UAAs combined
    with conventional site-directed mutagenesis and molecular dynamics simulations,
    we discover that pore opening involves a widening of interfaces formed by TM3
    with non-pore-lining TMs. Orai1 mutants with a UAA in TM3 exhibit weaker STIM1-induced
    activation after UV exposure, possibly caused by a restricted widening of non-pore-lining
    TM interfaces. We demonstrate that photocrosslinking UAAs are excellent tools
    for improving our understanding of key determinants and ion channel dynamics modulating
    pore opening.
acknowledgement: We thank S. Buchegger for excellent technical assistance. This research
  was funded by the Austrian Science Fund (FWF) projects https://doi.org/10.55776/P32851,
  https://doi.org/10.55776/P35900, and https://doi.org/10.55776/P36202 to I.D. and
  https://doi.org/10.55776/PAT6871323 to A.T. N.M. is funded within the DOC program
  of the OeAW (Austrian Academy of Science). For open access purposes, the author
  has applied a CC BY public copyright license to any author-accepted manuscript version
  arising from this submission.
article_number: '102623'
article_processing_charge: Yes
article_type: original
author:
- first_name: Hadil
  full_name: Najjar, Hadil
  last_name: Najjar
- first_name: Sarah
  full_name: Weiß, Sarah
  last_name: Weiß
- first_name: Ferdinand
  full_name: Horvath, Ferdinand
  id: b0dc7f61-21a3-11ef-a9b4-e6ab1aa6f21e
  last_name: Horvath
- first_name: Valentina
  full_name: Hopl, Valentina
  last_name: Hopl
- first_name: Adéla
  full_name: Tiffner, Adéla
  last_name: Tiffner
- first_name: Lorenz
  full_name: Höbarth, Lorenz
  last_name: Höbarth
- first_name: Julia
  full_name: Söllner, Julia
  last_name: Söllner
- first_name: Maximilian
  full_name: Fröhlich, Maximilian
  last_name: Fröhlich
- first_name: Magdalena
  full_name: Prantl, Magdalena
  last_name: Prantl
- first_name: Nora
  full_name: Müller, Nora
  last_name: Müller
- first_name: Yuliia
  full_name: Nazarenko, Yuliia
  last_name: Nazarenko
- first_name: Selina
  full_name: Harant, Selina
  last_name: Harant
- first_name: Lukas
  full_name: Weissenböck, Lukas
  last_name: Weissenböck
- first_name: Herwig
  full_name: Grabmayr, Herwig
  last_name: Grabmayr
- first_name: Matthias
  full_name: Sallinger, Matthias
  last_name: Sallinger
- first_name: Lena
  full_name: Maltan, Lena
  last_name: Maltan
- first_name: Linda V.
  full_name: Echefu, Linda V.
  last_name: Echefu
- first_name: Tamara
  full_name: Radiskovic, Tamara
  last_name: Radiskovic
- first_name: Melanie
  full_name: Leopold, Melanie
  last_name: Leopold
- first_name: Sonja
  full_name: Lindinger, Sonja
  last_name: Lindinger
- first_name: Christina
  full_name: Humer, Christina
  last_name: Humer
- first_name: Carmen
  full_name: Höglinger, Carmen
  last_name: Höglinger
- first_name: Heinrich
  full_name: Krobath, Heinrich
  last_name: Krobath
- first_name: Thomas
  full_name: Renger, Thomas
  last_name: Renger
- first_name: Isabella
  full_name: Derler, Isabella
  last_name: Derler
citation:
  ama: Najjar H, Weiß S, Horvath F, et al. STIM1-induced widening of non-pore-lining
    TM interfaces is crucial for Orai1 pore opening. <i>Cell Reports Physical Science</i>.
    2025;6(6). doi:<a href="https://doi.org/10.1016/j.xcrp.2025.102623">10.1016/j.xcrp.2025.102623</a>
  apa: Najjar, H., Weiß, S., Horvath, F., Hopl, V., Tiffner, A., Höbarth, L., … Derler,
    I. (2025). STIM1-induced widening of non-pore-lining TM interfaces is crucial
    for Orai1 pore opening. <i>Cell Reports Physical Science</i>. Cell Press. <a href="https://doi.org/10.1016/j.xcrp.2025.102623">https://doi.org/10.1016/j.xcrp.2025.102623</a>
  chicago: Najjar, Hadil, Sarah Weiß, Ferdinand Horvath, Valentina Hopl, Adéla Tiffner,
    Lorenz Höbarth, Julia Söllner, et al. “STIM1-Induced Widening of Non-Pore-Lining
    TM Interfaces Is Crucial for Orai1 Pore Opening.” <i>Cell Reports Physical Science</i>.
    Cell Press, 2025. <a href="https://doi.org/10.1016/j.xcrp.2025.102623">https://doi.org/10.1016/j.xcrp.2025.102623</a>.
  ieee: H. Najjar <i>et al.</i>, “STIM1-induced widening of non-pore-lining TM interfaces
    is crucial for Orai1 pore opening,” <i>Cell Reports Physical Science</i>, vol.
    6, no. 6. Cell Press, 2025.
  ista: Najjar H, Weiß S, Horvath F, Hopl V, Tiffner A, Höbarth L, Söllner J, Fröhlich
    M, Prantl M, Müller N, Nazarenko Y, Harant S, Weissenböck L, Grabmayr H, Sallinger
    M, Maltan L, Echefu LV, Radiskovic T, Leopold M, Lindinger S, Humer C, Höglinger
    C, Krobath H, Renger T, Derler I. 2025. STIM1-induced widening of non-pore-lining
    TM interfaces is crucial for Orai1 pore opening. Cell Reports Physical Science.
    6(6), 102623.
  mla: Najjar, Hadil, et al. “STIM1-Induced Widening of Non-Pore-Lining TM Interfaces
    Is Crucial for Orai1 Pore Opening.” <i>Cell Reports Physical Science</i>, vol.
    6, no. 6, 102623, Cell Press, 2025, doi:<a href="https://doi.org/10.1016/j.xcrp.2025.102623">10.1016/j.xcrp.2025.102623</a>.
  short: H. Najjar, S. Weiß, F. Horvath, V. Hopl, A. Tiffner, L. Höbarth, J. Söllner,
    M. Fröhlich, M. Prantl, N. Müller, Y. Nazarenko, S. Harant, L. Weissenböck, H.
    Grabmayr, M. Sallinger, L. Maltan, L.V. Echefu, T. Radiskovic, M. Leopold, S.
    Lindinger, C. Humer, C. Höglinger, H. Krobath, T. Renger, I. Derler, Cell Reports
    Physical Science 6 (2025).
date_created: 2025-06-15T22:01:31Z
date_published: 2025-06-18T00:00:00Z
date_updated: 2026-10-20T08:25:34Z
day: '18'
ddc:
- '570'
department:
- _id: AnSa
doi: 10.1016/j.xcrp.2025.102623
external_id:
  isi:
  - '001516570500009'
file:
- access_level: open_access
  checksum: 37ff7c396f966d0ec363e4691d63d402
  content_type: application/pdf
  creator: dernst
  date_created: 2025-06-23T10:20:22Z
  date_updated: 2025-06-23T10:20:22Z
  file_id: '19868'
  file_name: 2025_CellReportsPhysicalScience_Najjar.pdf
  file_size: 9771117
  relation: main_file
  success: 1
file_date_updated: 2025-06-23T10:20:22Z
fulldoi: https://doi.org/10.1016/j.xcrp.2025.102623
has_accepted_license: '1'
intvolume: '         6'
isi: 1
issue: '6'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: Cell Reports Physical Science
publication_identifier:
  eissn:
  - 2666-3864
publication_status: published
publisher: Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: STIM1-induced widening of non-pore-lining TM interfaces is crucial for Orai1
  pore opening
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6
year: '2025'
...
---
OA_place: publisher
OA_type: hybrid
_id: '20029'
abstract:
- lang: eng
  text: Vacuolar acidification is crucial for the homeostasis of intracellular pH
    and the recycling of proteins and nutrients in cells, thereby playing important
    roles in various physiological processes related to vacuolar function. The key
    factors regulating vacuolar acidification and underlying mechanisms remain unclear.
    Here, we report that Arabidopsis phospholipase Dζ2 (PLDζ2) promotes the acidification
    of the vacuolar lumen to stimulate autophagic degradation under phosphorus deficiency.
    The pldζ2 mutant massively accumulates autophagic structures while exhibiting
    premature leaf senescence under nutrient starvation. Impaired autophagic flux,
    lytic vacuole morphology, and lytic degradation in pldζ2 indicate that PLDζ2 regulates
    autophagy by affecting the vacuolar function. PLDζ2 locates in both tonoplast
    and cytoplasm. Genetic, structural, and biochemical studies demonstrate that PLDζ2
    directly interacts with vacuolar-type ATPase (V-ATPase) subunit D (VATD) to promote
    vacuolar acidification and autophagy under phosphorus starvation. These findings
    reveal the importance of V-ATPase and vacuolar pH in autophagic activity and provide
    clues in elucidating the regulatory mechanism of vacuolar acidification.
acknowledgement: The study was supported by National Natural Science Foundation of
  China (NSFC, 92354301, 32230011, 32200274, and 91954206). The computations were
  run on the Siyuan-1 cluster supported by the Center for High-Performance Computing
  at Shanghai Jiao Tong University.
article_number: '116024'
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Bin
  full_name: Guan, Bin
  id: 56aad729-cca2-11ed-a45a-9b4138991a48
  last_name: Guan
- first_name: Ke Xuan
  full_name: Xie, Ke Xuan
  last_name: Xie
- first_name: Xin Qiao
  full_name: Du, Xin Qiao
  last_name: Du
- first_name: Yu Xuan
  full_name: Bai, Yu Xuan
  last_name: Bai
- first_name: Peng Chao
  full_name: Hao, Peng Chao
  last_name: Hao
- first_name: Wen Hui
  full_name: Lin, Wen Hui
  last_name: Lin
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Hong Wei
  full_name: Xue, Hong Wei
  last_name: Xue
citation:
  ama: Guan B, Xie KX, Du XQ, et al. Arabidopsis phospholipase Dζ2 facilitates vacuolar
    acidification and autophagy under phosphorus starvation by interacting with VATD.
    <i>Cell Reports</i>. 2025;44(7). doi:<a href="https://doi.org/10.1016/j.celrep.2025.116024">10.1016/j.celrep.2025.116024</a>
  apa: Guan, B., Xie, K. X., Du, X. Q., Bai, Y. X., Hao, P. C., Lin, W. H., … Xue,
    H. W. (2025). Arabidopsis phospholipase Dζ2 facilitates vacuolar acidification
    and autophagy under phosphorus starvation by interacting with VATD. <i>Cell Reports</i>.
    Cell Press. <a href="https://doi.org/10.1016/j.celrep.2025.116024">https://doi.org/10.1016/j.celrep.2025.116024</a>
  chicago: Guan, Bin, Ke Xuan Xie, Xin Qiao Du, Yu Xuan Bai, Peng Chao Hao, Wen Hui
    Lin, Jiří Friml, and Hong Wei Xue. “Arabidopsis Phospholipase Dζ2 Facilitates
    Vacuolar Acidification and Autophagy under Phosphorus Starvation by Interacting
    with VATD.” <i>Cell Reports</i>. Cell Press, 2025. <a href="https://doi.org/10.1016/j.celrep.2025.116024">https://doi.org/10.1016/j.celrep.2025.116024</a>.
  ieee: B. Guan <i>et al.</i>, “Arabidopsis phospholipase Dζ2 facilitates vacuolar
    acidification and autophagy under phosphorus starvation by interacting with VATD,”
    <i>Cell Reports</i>, vol. 44, no. 7. Cell Press, 2025.
  ista: Guan B, Xie KX, Du XQ, Bai YX, Hao PC, Lin WH, Friml J, Xue HW. 2025. Arabidopsis
    phospholipase Dζ2 facilitates vacuolar acidification and autophagy under phosphorus
    starvation by interacting with VATD. Cell Reports. 44(7), 116024.
  mla: Guan, Bin, et al. “Arabidopsis Phospholipase Dζ2 Facilitates Vacuolar Acidification
    and Autophagy under Phosphorus Starvation by Interacting with VATD.” <i>Cell Reports</i>,
    vol. 44, no. 7, 116024, Cell Press, 2025, doi:<a href="https://doi.org/10.1016/j.celrep.2025.116024">10.1016/j.celrep.2025.116024</a>.
  short: B. Guan, K.X. Xie, X.Q. Du, Y.X. Bai, P.C. Hao, W.H. Lin, J. Friml, H.W.
    Xue, Cell Reports 44 (2025).
date_created: 2025-07-20T22:02:01Z
date_published: 2025-07-22T00:00:00Z
date_updated: 2026-10-20T08:22:53Z
day: '22'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1016/j.celrep.2025.116024
external_id:
  isi:
  - '001533244800001'
  pmid:
  - '40668679'
file:
- access_level: open_access
  checksum: ee03deee47a084b0295251dc49470ad4
  content_type: application/pdf
  creator: dernst
  date_created: 2025-07-22T08:52:17Z
  date_updated: 2025-07-22T08:52:17Z
  file_id: '20067'
  file_name: 2025_CellReports_Guan.pdf
  file_size: 37708120
  relation: main_file
  success: 1
file_date_updated: 2025-07-22T08:52:17Z
fulldoi: https://doi.org/10.1016/j.celrep.2025.116024
has_accepted_license: '1'
intvolume: '        44'
isi: 1
issue: '7'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
  issn:
  - 2639-1856
publication_status: published
publisher: Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Arabidopsis phospholipase Dζ2 facilitates vacuolar acidification and autophagy
  under phosphorus starvation by interacting with VATD
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
  short: CC BY-NC (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 44
year: '2025'
...
---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '20116'
abstract:
- lang: eng
  text: Auxin regulates various aspects of plant growth and development by modulating
    the transcription of target genes through the degradation of auxin/indole-3-acetic
    acid (Aux/IAA) repressors via the 26S proteasome. Proteasome regulator 1 (PTRE1),
    a positive regulator of proteasome activity, has been implicated in auxin-mediated
    proteasome suppression; however, the mechanism by which auxin modulates PTRE1
    function remains unclear. Here, we demonstrate that auxin promotes the interaction
    between germin-like protein 1 (GLP1) and PTRE1, facilitating PTRE1 retention at
    the plasma membrane. The relocation of PTRE1 results in reduced nuclear 26S proteasome
    activity, and thus the attenuated Aux/IAA degradation and altered Aux/IAA homeostasis,
    ultimately resulting in suppressed auxin-mediated transcriptional regulation.
    Our findings uncover a previously uncharacterized regulatory axis in auxin signaling
    that controls Aux/IAA protein stability, functioning alongside the TIR1- and TRANSMEMBRANE
    KINASE 1 (TMK1)-mediated pathways, and highlight the coordination of auxin signaling
    from the cell surface to the nucleus via auxin-induced PTRE1 relocation, which
    fine-tunes Aux/IAA protein homeostasis and auxin responses.
acknowledgement: The study was supported by the National Natural Science Foundation
  of China (NSFC; 32230011, 91954206, and 31721001). We thank Dr. Deli Lin (Shanghai
  Jiao Tong University) for kind help with the laser confocal microscope observation
  and the Arabidopsis Biological Resource Center (ABRC) for providing T-DNA insertional
  mutants.
article_number: '116056'
article_processing_charge: Yes
article_type: original
author:
- first_name: Faqing
  full_name: Xu, Faqing
  last_name: Xu
- first_name: Yongqiang
  full_name: Yu, Yongqiang
  last_name: Yu
- first_name: Bin
  full_name: Guan, Bin
  id: 56aad729-cca2-11ed-a45a-9b4138991a48
  last_name: Guan
- first_name: Tongda
  full_name: Xu, Tongda
  last_name: Xu
- first_name: Zhihong
  full_name: Xu, Zhihong
  last_name: Xu
- first_name: Hongwei
  full_name: Xue, Hongwei
  last_name: Xue
citation:
  ama: Xu F, Yu Y, Guan B, Xu T, Xu Z, Xue H. Germin-like protein 1 interacts with
    proteasome regulator 1 to regulate auxin signaling by controlling Aux/IAA homeostasis.
    <i>Cell Reports</i>. 2025;44(8). doi:<a href="https://doi.org/10.1016/j.celrep.2025.116056">10.1016/j.celrep.2025.116056</a>
  apa: Xu, F., Yu, Y., Guan, B., Xu, T., Xu, Z., &#38; Xue, H. (2025). Germin-like
    protein 1 interacts with proteasome regulator 1 to regulate auxin signaling by
    controlling Aux/IAA homeostasis. <i>Cell Reports</i>. Cell Press. <a href="https://doi.org/10.1016/j.celrep.2025.116056">https://doi.org/10.1016/j.celrep.2025.116056</a>
  chicago: Xu, Faqing, Yongqiang Yu, Bin Guan, Tongda Xu, Zhihong Xu, and Hongwei
    Xue. “Germin-like Protein 1 Interacts with Proteasome Regulator 1 to Regulate
    Auxin Signaling by Controlling Aux/IAA Homeostasis.” <i>Cell Reports</i>. Cell
    Press, 2025. <a href="https://doi.org/10.1016/j.celrep.2025.116056">https://doi.org/10.1016/j.celrep.2025.116056</a>.
  ieee: F. Xu, Y. Yu, B. Guan, T. Xu, Z. Xu, and H. Xue, “Germin-like protein 1 interacts
    with proteasome regulator 1 to regulate auxin signaling by controlling Aux/IAA
    homeostasis,” <i>Cell Reports</i>, vol. 44, no. 8. Cell Press, 2025.
  ista: Xu F, Yu Y, Guan B, Xu T, Xu Z, Xue H. 2025. Germin-like protein 1 interacts
    with proteasome regulator 1 to regulate auxin signaling by controlling Aux/IAA
    homeostasis. Cell Reports. 44(8), 116056.
  mla: Xu, Faqing, et al. “Germin-like Protein 1 Interacts with Proteasome Regulator
    1 to Regulate Auxin Signaling by Controlling Aux/IAA Homeostasis.” <i>Cell Reports</i>,
    vol. 44, no. 8, 116056, Cell Press, 2025, doi:<a href="https://doi.org/10.1016/j.celrep.2025.116056">10.1016/j.celrep.2025.116056</a>.
  short: F. Xu, Y. Yu, B. Guan, T. Xu, Z. Xu, H. Xue, Cell Reports 44 (2025).
date_created: 2025-08-04T13:39:11Z
date_published: 2025-07-24T00:00:00Z
date_updated: 2026-10-20T08:23:15Z
day: '24'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1016/j.celrep.2025.116056
external_id:
  isi:
  - '001542038500001'
  pmid:
  - '40714631'
file:
- access_level: open_access
  checksum: 3c43e040a4a7a65ec67ae1d2bb81261a
  content_type: application/pdf
  creator: dernst
  date_created: 2025-08-05T06:15:09Z
  date_updated: 2025-08-05T06:15:09Z
  file_id: '20120'
  file_name: 2025_CellReports_Xu.pdf
  file_size: 24178018
  relation: main_file
  success: 1
file_date_updated: 2025-08-05T06:15:09Z
fulldoi: https://doi.org/10.1016/j.celrep.2025.116056
has_accepted_license: '1'
intvolume: '        44'
isi: 1
issue: '8'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Germin-like protein 1 interacts with proteasome regulator 1 to regulate auxin
  signaling by controlling Aux/IAA homeostasis
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
  short: CC BY-NC (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 44
year: '2025'
...
