---
_id: '15318'
abstract:
- lang: eng
  text: We consider a gas of N weakly interacting bosons in the ground state. Such
    gases exhibit Bose–Einstein condensation. The binding energy is defined as the
    energy it takes to remove one particle from the gas. In this article, we prove
    an asymptotic expansion for the binding energy, and compute the first orders explicitly
    for the homogeneous gas. Our result addresses in particular a conjecture by Nam
    (Lett Math Phys 108(1):141–159, 2018), and provides an asymptotic expansion of
    the ionization energy of bosonic atoms.
acknowledgement: "It is a pleasure to thank Phan Thành Nam for helpful discussions
  on bosonic atoms. L.B. was supported by the German Research Foundation within the
  Munich Center of Quantum Science and Technology (EXC 2111). N.L. gratefully acknowledges
  support from the Swiss National Science Foundation through the NCCR SwissMap and
  funding from the European Union’s Horizon 2020 research and innovation programme
  under the Marie Skłodowska-Curie Grant agreement No 101024712. S.P. acknowledges
  funding by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—Project
  number 512258249.\r\nOpen Access funding enabled and organized by Projekt DEAL."
article_number: '48'
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Lea
  full_name: Bossmann, Lea
  id: A2E3BCBE-5FCC-11E9-AA4B-76F3E5697425
  last_name: Bossmann
  orcid: 0000-0002-6854-1343
- first_name: Nikolai K
  full_name: Leopold, Nikolai K
  id: 4BC40BEC-F248-11E8-B48F-1D18A9856A87
  last_name: Leopold
  orcid: 0000-0002-0495-6822
- first_name: David Johannes
  full_name: Mitrouskas, David Johannes
  id: cbddacee-2b11-11eb-a02e-a2e14d04e52d
  last_name: Mitrouskas
- first_name: Sören P
  full_name: Petrat, Sören P
  id: 40AC02DC-F248-11E8-B48F-1D18A9856A87
  last_name: Petrat
  orcid: 0000-0002-9166-5889
citation:
  ama: Bossmann L, Leopold NK, Mitrouskas DJ, Petrat SP. A note on the binding energy
    for Bosons in the mean-field limit. <i>Journal of Statistical Physics</i>. 2024;191(4).
    doi:<a href="https://doi.org/10.1007/s10955-024-03260-5">10.1007/s10955-024-03260-5</a>
  apa: Bossmann, L., Leopold, N. K., Mitrouskas, D. J., &#38; Petrat, S. P. (2024).
    A note on the binding energy for Bosons in the mean-field limit. <i>Journal of
    Statistical Physics</i>. Springer Nature. <a href="https://doi.org/10.1007/s10955-024-03260-5">https://doi.org/10.1007/s10955-024-03260-5</a>
  chicago: Bossmann, Lea, Nikolai K Leopold, David Johannes Mitrouskas, and Sören
    P Petrat. “A Note on the Binding Energy for Bosons in the Mean-Field Limit.” <i>Journal
    of Statistical Physics</i>. Springer Nature, 2024. <a href="https://doi.org/10.1007/s10955-024-03260-5">https://doi.org/10.1007/s10955-024-03260-5</a>.
  ieee: L. Bossmann, N. K. Leopold, D. J. Mitrouskas, and S. P. Petrat, “A note on
    the binding energy for Bosons in the mean-field limit,” <i>Journal of Statistical
    Physics</i>, vol. 191, no. 4. Springer Nature, 2024.
  ista: Bossmann L, Leopold NK, Mitrouskas DJ, Petrat SP. 2024. A note on the binding
    energy for Bosons in the mean-field limit. Journal of Statistical Physics. 191(4),
    48.
  mla: Bossmann, Lea, et al. “A Note on the Binding Energy for Bosons in the Mean-Field
    Limit.” <i>Journal of Statistical Physics</i>, vol. 191, no. 4, 48, Springer Nature,
    2024, doi:<a href="https://doi.org/10.1007/s10955-024-03260-5">10.1007/s10955-024-03260-5</a>.
  short: L. Bossmann, N.K. Leopold, D.J. Mitrouskas, S.P. Petrat, Journal of Statistical
    Physics 191 (2024).
das_tickbox: '1'
dataavailabilitystatement: Data sharing not applicable to this article as no datasets
  were generated or analyzed during the current study.
date_created: 2024-04-14T22:01:02Z
date_published: 2024-04-06T00:00:00Z
date_updated: 2026-09-17T11:05:18Z
day: '06'
ddc:
- '510'
department:
- _id: RoSe
doi: 10.1007/s10955-024-03260-5
external_id:
  arxiv:
  - '2307.13115'
  isi:
  - '001197663100002'
file:
- access_level: open_access
  checksum: 839242a9ec1c01158112de25f196e60d
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  creator: dernst
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has_accepted_license: '1'
intvolume: '       191'
isi: 1
issue: '4'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
publication: Journal of Statistical Physics
publication_identifier:
  eissn:
  - 1572-9613
  issn:
  - 0022-4715
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
researchdata_availability: not applicable
scopus_import: '1'
status: public
supplementarymaterial: no
title: A note on the binding energy for Bosons in the mean-field limit
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: 191
year: '2024'
...
---
OA_place: publisher
OA_type: hybrid
_id: '17478'
abstract:
- lang: eng
  text: "We study the Fröhlich polaron model in R3, and prove a lower bound on its
    ground state energy as a function of the total momentum. The bound is asymptotically
    sharp at large coupling. In combination with a corresponding upper bound proved
    earlier (Mitrouskas et al. in Forum Math. Sigma 11:1–52, 2023), it shows that
    the energy is approximately parabolic below the continuum threshold, and that
    the polaron’s effective mass (defined as the semi-latus rectum of the\r\nparabola)
    is given by the celebrated Landau–Pekar formula. In particular, it diverges as
    α4 for large coupling constant α."
article_processing_charge: Yes (in subscription journal)
article_type: original
arxiv: 1
author:
- first_name: Morris
  full_name: Brooks, Morris
  id: B7ECF9FC-AA38-11E9-AC9A-0930E6697425
  last_name: Brooks
  orcid: 0000-0002-6249-0928
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
citation:
  ama: 'Brooks M, Seiringer R. The Fröhlich polaron at strong coupling: Part II —
    Energy-momentum relation and effective mass. <i>Publications Mathematiques de
    l’Institut des Hautes Etudes Scientifiques</i>. 2024;140:271-309. doi:<a href="https://doi.org/10.1007/s10240-024-00150-0">10.1007/s10240-024-00150-0</a>'
  apa: 'Brooks, M., &#38; Seiringer, R. (2024). The Fröhlich polaron at strong coupling:
    Part II — Energy-momentum relation and effective mass. <i>Publications Mathematiques
    de l’Institut Des Hautes Etudes Scientifiques</i>. Springer Nature. <a href="https://doi.org/10.1007/s10240-024-00150-0">https://doi.org/10.1007/s10240-024-00150-0</a>'
  chicago: 'Brooks, Morris, and Robert Seiringer. “The Fröhlich Polaron at Strong
    Coupling: Part II — Energy-Momentum Relation and Effective Mass.” <i>Publications
    Mathematiques de l’Institut Des Hautes Etudes Scientifiques</i>. Springer Nature,
    2024. <a href="https://doi.org/10.1007/s10240-024-00150-0">https://doi.org/10.1007/s10240-024-00150-0</a>.'
  ieee: 'M. Brooks and R. Seiringer, “The Fröhlich polaron at strong coupling: Part
    II — Energy-momentum relation and effective mass,” <i>Publications Mathematiques
    de l’Institut des Hautes Etudes Scientifiques</i>, vol. 140. Springer Nature,
    pp. 271–309, 2024.'
  ista: 'Brooks M, Seiringer R. 2024. The Fröhlich polaron at strong coupling: Part
    II — Energy-momentum relation and effective mass. Publications Mathematiques de
    l’Institut des Hautes Etudes Scientifiques. 140, 271–309.'
  mla: 'Brooks, Morris, and Robert Seiringer. “The Fröhlich Polaron at Strong Coupling:
    Part II — Energy-Momentum Relation and Effective Mass.” <i>Publications Mathematiques
    de l’Institut Des Hautes Etudes Scientifiques</i>, vol. 140, Springer Nature,
    2024, pp. 271–309, doi:<a href="https://doi.org/10.1007/s10240-024-00150-0">10.1007/s10240-024-00150-0</a>.'
  short: M. Brooks, R. Seiringer, Publications Mathematiques de l’Institut Des Hautes
    Etudes Scientifiques 140 (2024) 271–309.
corr_author: '1'
das_tickbox: '0'
date_created: 2024-09-01T22:01:08Z
date_published: 2024-12-01T00:00:00Z
date_updated: 2026-09-17T11:07:19Z
day: '01'
ddc:
- '510'
department:
- _id: RoSe
doi: 10.1007/s10240-024-00150-0
external_id:
  arxiv:
  - '2211.03353'
  isi:
  - '001297785000001'
file:
- access_level: open_access
  checksum: af3becc50f7534c9409d3ff8b5c47ed6
  content_type: application/pdf
  creator: dernst
  date_created: 2025-01-13T08:13:42Z
  date_updated: 2025-01-13T08:13:42Z
  file_id: '18824'
  file_name: 2024_PublicMathIHES_Brooks.pdf
  file_size: 924342
  relation: main_file
  success: 1
file_date_updated: 2025-01-13T08:13:42Z
fulldoi: https://doi.org/10.1007/s10240-024-00150-0
has_accepted_license: '1'
intvolume: '       140'
isi: 1
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 271-309
publication: Publications Mathematiques de l'Institut des Hautes Etudes Scientifiques
publication_identifier:
  eissn:
  - 1618-1913
  issn:
  - 0073-8301
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: yes
title: 'The Fröhlich polaron at strong coupling: Part II — Energy-momentum relation
  and effective mass'
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: 140
year: '2024'
...
---
OA_place: repository
OA_type: green
_id: '18948'
abstract:
- lang: eng
  text: We consider a gas of N bosons with interactions in the mean-field scaling
    regime. We review a recent proof of the asymptotic expansion of its spectrum and
    eigenstates and two applications of this result, namely the derivation of an Edgeworth
    expansion for fluctuations of one-body operators and the computation of the binding
    energy of an inhomogeneous Bose gas to any order. Finally, we collect related
    results for the dynamics of the weakly interacting Bose gas and for the regularized
    Nelson model.
acknowledgement: It is our pleasure to thank Marco Falconi, Nataša Pavlović, Peter
  Pickl, Robert Seiringer and Avy Soffer for the collaboration on the works [11, 13,
  14, 21, 33, 39]. L.B. was supported by the German Research Foundation within the
  Munich Center of Quantum Science and Technology (EXC 2111). N.L. acknowledges support
  from the Swiss National Science Foundation through the NCCR SwissMap and funding
  from the European Union’s Horizon 2020 research and innovation programme under the
  Marie Skłodowska-Curie grant agreement No 101024712. S.P. acknowledges funding by
  the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - project
  number 512258249.
alternative_title:
- Fundamental Theories of Physics
article_processing_charge: No
arxiv: 1
author:
- first_name: Lea
  full_name: Bossmann, Lea
  id: A2E3BCBE-5FCC-11E9-AA4B-76F3E5697425
  last_name: Bossmann
  orcid: 0000-0002-6854-1343
- first_name: Nikolai
  full_name: Leopold, Nikolai
  last_name: Leopold
- first_name: David Johannes
  full_name: Mitrouskas, David Johannes
  id: cbddacee-2b11-11eb-a02e-a2e14d04e52d
  last_name: Mitrouskas
- first_name: Sören
  full_name: Petrat, Sören
  last_name: Petrat
citation:
  ama: 'Bossmann L, Leopold N, Mitrouskas DJ, Petrat S. Asymptotic Analysis of the Weakly
    Interacting Bose Gas: A Collection of Recent Results and Applications. In: Bassi
    A, Goldstein S, Tumulka R, Zanghi N, eds. <i>Physics and the Nature of Reality</i>.
    Vol 215. FTPH. Cham: Springer Nature; 2024:307-321. doi:<a href="https://doi.org/10.1007/978-3-031-45434-9_22">10.1007/978-3-031-45434-9_22</a>'
  apa: 'Bossmann, L., Leopold, N., Mitrouskas, D. J., &#38; Petrat, S. (2024). Asymptotic
    Analysis of the Weakly Interacting Bose Gas: A Collection of Recent Results and Applications.
    In A. Bassi, S. Goldstein, R. Tumulka, &#38; N. Zanghi (Eds.), <i>Physics and
    the Nature of Reality</i> (Vol. 215, pp. 307–321). Cham: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-45434-9_22">https://doi.org/10.1007/978-3-031-45434-9_22</a>'
  chicago: 'Bossmann, Lea, Nikolai Leopold, David Johannes Mitrouskas, and Sören Petrat.
    “Asymptotic Analysis of the Weakly Interacting Bose Gas: A Collection of Recent
    Results and Applications.” In <i>Physics and the Nature of Reality</i>, edited
    by Angelo Bassi, Sheldon Goldstein, Roderich Tumulka, and Nino Zanghi, 215:307–21.
    FTPH. Cham: Springer Nature, 2024. <a href="https://doi.org/10.1007/978-3-031-45434-9_22">https://doi.org/10.1007/978-3-031-45434-9_22</a>.'
  ieee: 'L. Bossmann, N. Leopold, D. J. Mitrouskas, and S. Petrat, “Asymptotic Analysis
    of the Weakly Interacting Bose Gas: A Collection of Recent Results and Applications,”
    in <i>Physics and the Nature of Reality</i>, vol. 215, A. Bassi, S. Goldstein,
    R. Tumulka, and N. Zanghi, Eds. Cham: Springer Nature, 2024, pp. 307–321.'
  ista: 'Bossmann L, Leopold N, Mitrouskas DJ, Petrat S. 2024.Asymptotic Analysis
    of the Weakly Interacting Bose Gas: A Collection of Recent Results and Applications.
    In: Physics and the Nature of Reality. Fundamental Theories of Physics, vol. 215,
    307–321.'
  mla: 'Bossmann, Lea, et al. “Asymptotic Analysis of the Weakly Interacting Bose
    Gas: A Collection of Recent Results and Applications.” <i>Physics and the Nature
    of Reality</i>, edited by Angelo Bassi et al., vol. 215, Springer Nature, 2024,
    pp. 307–21, doi:<a href="https://doi.org/10.1007/978-3-031-45434-9_22">10.1007/978-3-031-45434-9_22</a>.'
  short: L. Bossmann, N. Leopold, D.J. Mitrouskas, S. Petrat, in:, A. Bassi, S. Goldstein,
    R. Tumulka, N. Zanghi (Eds.), Physics and the Nature of Reality, Springer Nature,
    Cham, 2024, pp. 307–321.
das_tickbox: '0'
date_created: 2025-01-29T10:30:08Z
date_published: 2024-02-04T00:00:00Z
date_updated: 2026-09-17T11:08:01Z
day: '04'
department:
- _id: RoSe
doi: 10.1007/978-3-031-45434-9_22
editor:
- first_name: Angelo
  full_name: Bassi, Angelo
  last_name: Bassi
- first_name: Sheldon
  full_name: Goldstein, Sheldon
  last_name: Goldstein
- first_name: Roderich
  full_name: Tumulka, Roderich
  last_name: Tumulka
- first_name: Nino
  full_name: Zanghi, Nino
  last_name: Zanghi
external_id:
  arxiv:
  - '2304.12910'
fulldoi: https://doi.org/10.1007/978-3-031-45434-9_22
intvolume: '       215'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2304.12910
month: '02'
oa: 1
oa_version: Preprint
page: 307-321
place: Cham
publication: Physics and the Nature of Reality
publication_identifier:
  eisbn:
  - '9783031454349'
  eissn:
  - 2365-6425
  isbn:
  - '9783031454332'
  issn:
  - 0168-1222
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
series_title: FTPH
status: public
supplementarymaterial: no
title: 'Asymptotic Analysis of the Weakly Interacting Bose Gas: A Collection of Recent
  Results and Applications'
type: book_chapter
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 215
year: '2024'
...
---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '17457'
abstract:
- lang: eng
  text: "Autoantibodies against the protein leucine-rich glioma inactivated 1 (LGI1)
    cause the most\r\ncommon subtype of autoimmune encephalitis with predominant involvement
    of the limbic\r\nsystem, associated with seizures and memory deficits. LGI1 and
    its receptor ADAM22 are part\r\nof a transsynaptic protein complex that includes
    several proteins involved in presynaptic\r\nneurotransmitter release and postsynaptic
    glutamate sensing. Autoantibodies against LGI1\r\nincrease excitatory synaptic
    strength, but studies that genetically disrupt the LGI1-ADAM22\r\ncomplex report
    a reduction in postsynaptic glutamate receptor-mediated responses. Thus, the\r\nmechanisms
    underlying the increased synaptic strength induced by LGI1 autoantibodies remain
    elusive, and the contributions of presynaptic molecules to the LGI1-transsynaptic
    complex remain unclear. We therefore investigated the presynaptic mechanisms that
    mediate\r\nautoantibody-induced synaptic strengthening."
acknowledged_ssus:
- _id: Bio
- _id: EM-Fac
acknowledgement: 'The authors thank Claudia Sommer for expert technical assistance,
  the Electron Microscopy Facility of IST-Austria for resources, and Tereza Belinova
  in the Imaging and Optics Facility of IST-Austria for 3D reconstruction. '
article_processing_charge: Yes
article_type: original
author:
- first_name: Andreas
  full_name: Ritzau-Jost, Andreas
  last_name: Ritzau-Jost
- first_name: Felix
  full_name: Gsell, Felix
  last_name: Gsell
- first_name: Josefine
  full_name: Sell, Josefine
  last_name: Sell
- first_name: Stefan
  full_name: Sachs, Stefan
  last_name: Sachs
- first_name: Jacqueline-Claire
  full_name: Montanaro-Punzengruber, Jacqueline-Claire
  id: 3786AB44-F248-11E8-B48F-1D18A9856A87
  last_name: Montanaro-Punzengruber
- first_name: Toni
  full_name: Kirmann, Toni
  last_name: Kirmann
- first_name: Sebastian
  full_name: Maaß, Sebastian
  last_name: Maaß
- first_name: Sarosh R.
  full_name: Irani, Sarosh R.
  last_name: Irani
- first_name: Christian
  full_name: Werner, Christian
  last_name: Werner
- first_name: Christian
  full_name: Geis, Christian
  last_name: Geis
- first_name: Markus
  full_name: Sauer, Markus
  last_name: Sauer
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Stefan
  full_name: Hallermann, Stefan
  last_name: Hallermann
citation:
  ama: Ritzau-Jost A, Gsell F, Sell J, et al. LGI1 autoantibodies enhance synaptic
    transmission by presynaptic Kv1 loss and increased action potential broadening.
    <i>Neurology, Neuroimmunology &#38; Neuroinflammation</i>. 2024;11(5):e200284.
    doi:<a href="https://doi.org/10.1212/NXI.0000000000200284">10.1212/NXI.0000000000200284</a>
  apa: Ritzau-Jost, A., Gsell, F., Sell, J., Sachs, S., Montanaro-Punzengruber, J.-C.,
    Kirmann, T., … Hallermann, S. (2024). LGI1 autoantibodies enhance synaptic transmission
    by presynaptic Kv1 loss and increased action potential broadening. <i>Neurology,
    Neuroimmunology &#38; Neuroinflammation</i>. Wolters Kluwer. <a href="https://doi.org/10.1212/NXI.0000000000200284">https://doi.org/10.1212/NXI.0000000000200284</a>
  chicago: Ritzau-Jost, Andreas, Felix Gsell, Josefine Sell, Stefan Sachs, Jacqueline-Claire
    Montanaro-Punzengruber, Toni Kirmann, Sebastian Maaß, et al. “LGI1 Autoantibodies
    Enhance Synaptic Transmission by Presynaptic Kv1 Loss and Increased Action Potential
    Broadening.” <i>Neurology, Neuroimmunology &#38; Neuroinflammation</i>. Wolters
    Kluwer, 2024. <a href="https://doi.org/10.1212/NXI.0000000000200284">https://doi.org/10.1212/NXI.0000000000200284</a>.
  ieee: A. Ritzau-Jost <i>et al.</i>, “LGI1 autoantibodies enhance synaptic transmission
    by presynaptic Kv1 loss and increased action potential broadening,” <i>Neurology,
    Neuroimmunology &#38; Neuroinflammation</i>, vol. 11, no. 5. Wolters Kluwer, p.
    e200284, 2024.
  ista: Ritzau-Jost A, Gsell F, Sell J, Sachs S, Montanaro-Punzengruber J-C, Kirmann
    T, Maaß S, Irani SR, Werner C, Geis C, Sauer M, Shigemoto R, Hallermann S. 2024.
    LGI1 autoantibodies enhance synaptic transmission by presynaptic Kv1 loss and
    increased action potential broadening. Neurology, Neuroimmunology &#38; Neuroinflammation.
    11(5), e200284.
  mla: Ritzau-Jost, Andreas, et al. “LGI1 Autoantibodies Enhance Synaptic Transmission
    by Presynaptic Kv1 Loss and Increased Action Potential Broadening.” <i>Neurology,
    Neuroimmunology &#38; Neuroinflammation</i>, vol. 11, no. 5, Wolters Kluwer, 2024,
    p. e200284, doi:<a href="https://doi.org/10.1212/NXI.0000000000200284">10.1212/NXI.0000000000200284</a>.
  short: A. Ritzau-Jost, F. Gsell, J. Sell, S. Sachs, J.-C. Montanaro-Punzengruber,
    T. Kirmann, S. Maaß, S.R. Irani, C. Werner, C. Geis, M. Sauer, R. Shigemoto, S.
    Hallermann, Neurology, Neuroimmunology &#38; Neuroinflammation 11 (2024) e200284.
das_tickbox: '1'
dataavailabilitystatement: Data that support the findings of this study are available
  from the corresponding author on reasonable request.
date_created: 2024-08-25T22:01:07Z
date_published: 2024-09-01T00:00:00Z
date_updated: 2026-09-17T11:27:41Z
day: '01'
ddc:
- '570'
department:
- _id: RySh
doi: 10.1212/NXI.0000000000200284
external_id:
  isi:
  - '001291908600001'
  pmid:
  - '39141878'
file:
- access_level: open_access
  checksum: 1e6d1230e0387f72752e3268f5330c9e
  content_type: application/pdf
  creator: dernst
  date_created: 2025-01-09T13:42:42Z
  date_updated: 2025-01-09T13:42:42Z
  file_id: '18815'
  file_name: 2024_NeurologyNeuroimmNeuroinflamm_RitzauJost.pdf
  file_size: 855818
  relation: main_file
  success: 1
file_date_updated: 2025-01-09T13:42:42Z
fulldoi: https://doi.org/10.1212/NXI.0000000000200284
has_accepted_license: '1'
intvolume: '        11'
isi: 1
issue: '5'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: e200284
pmid: 1
project:
- _id: 05970B30-7A3F-11EA-A408-12923DDC885E
  grant_number: I04638
  name: LGI1 antibody-induced pathophysiology in synapses
publication: Neurology, Neuroimmunology & Neuroinflammation
publication_identifier:
  eissn:
  - 2332-7812
publication_status: published
publisher: Wolters Kluwer
quality_controlled: '1'
related_material:
  link:
  - relation: earlier_version
    url: https://doi.org/10.1101/2023.10.04.560631
researchdata_availability: upon request
scopus_import: '1'
status: public
supplementarymaterial: yes
title: LGI1 autoantibodies enhance synaptic transmission by presynaptic Kv1 loss and
  increased action potential broadening
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: 11
year: '2024'
...
---
_id: '18958'
abstract:
- lang: eng
  text: This workshop brought together experts on the analysis of quantum many-body
    problems and quantum statistical mechanics, with the goal of discussing the state-of-the-art
    of the field, recent developments as well as challenges for the future. The main
    topics of discussion concerned the equilibrium and dynamical behavior of (bosonic
    or fermionic) quantum gases, quantum spin systems, as well as quantum field theory
    models like the Nelson or Fröhlich model.
acknowledgement: The MFO and the workshop organizers would like to thank the National
  Science Foundation for supporting the participation of junior researchers in the
  workshop by the grant DMS-2230648, “US Junior Oberwolfach Fellows”.
article_processing_charge: No
article_type: original
author:
- first_name: Christian
  full_name: Hainzl, Christian
  last_name: Hainzl
- first_name: Benjamin
  full_name: Schlein, Benjamin
  last_name: Schlein
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
- first_name: Simone
  full_name: Warzel, Simone
  last_name: Warzel
citation:
  ama: Hainzl C, Schlein B, Seiringer R, Warzel S. Many-body quantum systems. <i>Oberwolfach
    Reports</i>. 2024;20(3):2247-2302. doi:<a href="https://doi.org/10.4171/owr/2023/39">10.4171/owr/2023/39</a>
  apa: Hainzl, C., Schlein, B., Seiringer, R., &#38; Warzel, S. (2024). Many-body
    quantum systems. <i>Oberwolfach Reports</i>. EMS Press. <a href="https://doi.org/10.4171/owr/2023/39">https://doi.org/10.4171/owr/2023/39</a>
  chicago: Hainzl, Christian, Benjamin Schlein, Robert Seiringer, and Simone Warzel.
    “Many-Body Quantum Systems.” <i>Oberwolfach Reports</i>. EMS Press, 2024. <a href="https://doi.org/10.4171/owr/2023/39">https://doi.org/10.4171/owr/2023/39</a>.
  ieee: C. Hainzl, B. Schlein, R. Seiringer, and S. Warzel, “Many-body quantum systems,”
    <i>Oberwolfach Reports</i>, vol. 20, no. 3. EMS Press, pp. 2247–2302, 2024.
  ista: Hainzl C, Schlein B, Seiringer R, Warzel S. 2024. Many-body quantum systems.
    Oberwolfach Reports. 20(3), 2247–2302.
  mla: Hainzl, Christian, et al. “Many-Body Quantum Systems.” <i>Oberwolfach Reports</i>,
    vol. 20, no. 3, EMS Press, 2024, pp. 2247–302, doi:<a href="https://doi.org/10.4171/owr/2023/39">10.4171/owr/2023/39</a>.
  short: C. Hainzl, B. Schlein, R. Seiringer, S. Warzel, Oberwolfach Reports 20 (2024)
    2247–2302.
das_tickbox: '0'
date_created: 2025-01-29T13:09:28Z
date_published: 2024-04-18T00:00:00Z
date_updated: 2026-09-17T11:09:16Z
day: '18'
department:
- _id: RoSe
doi: 10.4171/owr/2023/39
fulldoi: https://doi.org/10.4171/owr/2023/39
intvolume: '        20'
issue: '3'
language:
- iso: eng
month: '04'
oa_version: None
page: 2247-2302
publication: Oberwolfach Reports
publication_identifier:
  eissn:
  - 1660-8941
  issn:
  - 1660-8933
publication_status: published
publisher: EMS Press
quality_controlled: '1'
researchdata_availability: no
status: public
supplementarymaterial: no
title: Many-body quantum systems
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 20
year: '2024'
...
---
_id: '14844'
abstract:
- lang: eng
  text: 'Many cell functions require a concerted effort from multiple membrane proteins,
    for example, for signaling, cell division, and endocytosis. One contribution to
    their successful self-organization stems from the membrane deformations that these
    proteins induce. While the pairwise interaction potential of two membrane-deforming
    spheres has recently been measured, membrane-deformation-induced interactions
    have been predicted to be nonadditive, and hence their collective behavior cannot
    be deduced from this measurement. We here employ a colloidal model system consisting
    of adhesive spheres and giant unilamellar vesicles to test these predictions by
    measuring the interaction potential of the simplest case of three membrane-deforming,
    spherical particles. We quantify their interactions and arrangements and, for
    the first time, experimentally confirm and quantify the nonadditive nature of
    membrane-deformation-induced interactions. We furthermore conclude that there
    exist two favorable configurations on the membrane: (1) a linear and (2) a triangular
    arrangement of the three spheres. Using Monte Carlo simulations, we corroborate
    the experimentally observed energy minima and identify a lowering of the membrane
    deformation as the cause for the observed configurations. The high symmetry of
    the preferred arrangements for three particles suggests that arrangements of many
    membrane-deforming objects might follow simple rules.'
acknowledgement: We gratefully acknowledge useful discussions with Casper van der
  Wel, help by Yogesh Shelke with PAA coverslip preparation, and support by Rachel
  Doherty with particle functionalization. A.A. and D.J.K. would like to thank Timon
  Idema and George Dadunashvili for initial attempts to simulate the experimental
  system. D.J.K. would like to thank the physics department at Leiden University for
  funding the PhD position of A.A. B.M. and A.Š. acknowledge funding by the European
  Union’s Horizon 2020 research and innovation programme (ERC starting grant no. 802960).
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Ali
  full_name: Azadbakht, Ali
  last_name: Azadbakht
- first_name: Billie
  full_name: Meadowcroft, Billie
  id: a4725fd6-932b-11ed-81e2-c098c7f37ae1
  last_name: Meadowcroft
  orcid: 0000-0003-3441-1337
- first_name: Juraj
  full_name: Majek, Juraj
  id: 3e6d9473-f38e-11ec-8ae0-c4e05a8aa9e1
  last_name: Majek
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Daniela J.
  full_name: Kraft, Daniela J.
  last_name: Kraft
citation:
  ama: Azadbakht A, Meadowcroft B, Majek J, Šarić A, Kraft DJ. Nonadditivity in interactions
    between three membrane-wrapped colloidal spheres. <i>Biophysical Journal</i>.
    2024;123(3):307-316. doi:<a href="https://doi.org/10.1016/j.bpj.2023.12.020">10.1016/j.bpj.2023.12.020</a>
  apa: Azadbakht, A., Meadowcroft, B., Majek, J., Šarić, A., &#38; Kraft, D. J. (2024).
    Nonadditivity in interactions between three membrane-wrapped colloidal spheres.
    <i>Biophysical Journal</i>. Elsevier. <a href="https://doi.org/10.1016/j.bpj.2023.12.020">https://doi.org/10.1016/j.bpj.2023.12.020</a>
  chicago: Azadbakht, Ali, Billie Meadowcroft, Juraj Majek, Anđela Šarić, and Daniela
    J. Kraft. “Nonadditivity in Interactions between Three Membrane-Wrapped Colloidal
    Spheres.” <i>Biophysical Journal</i>. Elsevier, 2024. <a href="https://doi.org/10.1016/j.bpj.2023.12.020">https://doi.org/10.1016/j.bpj.2023.12.020</a>.
  ieee: A. Azadbakht, B. Meadowcroft, J. Majek, A. Šarić, and D. J. Kraft, “Nonadditivity
    in interactions between three membrane-wrapped colloidal spheres,” <i>Biophysical
    Journal</i>, vol. 123, no. 3. Elsevier, pp. 307–316, 2024.
  ista: Azadbakht A, Meadowcroft B, Majek J, Šarić A, Kraft DJ. 2024. Nonadditivity
    in interactions between three membrane-wrapped colloidal spheres. Biophysical
    Journal. 123(3), 307–316.
  mla: Azadbakht, Ali, et al. “Nonadditivity in Interactions between Three Membrane-Wrapped
    Colloidal Spheres.” <i>Biophysical Journal</i>, vol. 123, no. 3, Elsevier, 2024,
    pp. 307–16, doi:<a href="https://doi.org/10.1016/j.bpj.2023.12.020">10.1016/j.bpj.2023.12.020</a>.
  short: A. Azadbakht, B. Meadowcroft, J. Majek, A. Šarić, D.J. Kraft, Biophysical
    Journal 123 (2024) 307–316.
das_tickbox: '0'
date_created: 2024-01-21T23:00:56Z
date_published: 2024-02-06T00:00:00Z
date_updated: 2026-09-24T10:26:59Z
day: '06'
ddc:
- '570'
department:
- _id: AnSa
doi: 10.1016/j.bpj.2023.12.020
ec_funded: 1
external_id:
  isi:
  - '001185235900001'
  pmid:
  - '38158654'
file:
- access_level: open_access
  checksum: 1c8fe1cf950394875b65b90da86428ff
  content_type: application/pdf
  creator: dernst
  date_created: 2024-07-16T12:09:55Z
  date_updated: 2024-07-16T12:09:55Z
  file_id: '17266'
  file_name: 2024_BiophysicalJournal_Azadbakht.pdf
  file_size: 3189926
  relation: main_file
  success: 1
file_date_updated: 2024-07-16T12:09:55Z
fulldoi: https://doi.org/10.1016/j.bpj.2023.12.020
has_accepted_license: '1'
intvolume: '       123'
isi: 1
issue: '3'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '02'
oa: 1
oa_version: Published Version
page: 307-316
pmid: 1
project:
- _id: eba2549b-77a9-11ec-83b8-a81e493eae4e
  call_identifier: H2020
  grant_number: '802960'
  name: 'Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines'
publication: Biophysical Journal
publication_identifier:
  eissn:
  - 1542-0086
  issn:
  - 0006-3495
publication_status: published
publisher: Elsevier
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: no
title: Nonadditivity in interactions between three membrane-wrapped colloidal spheres
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 123
year: '2024'
...
---
APC_amount: 5936,71 EUR
OA_place: publisher
OA_type: hybrid
_id: '15001'
abstract:
- lang: eng
  text: "Self-replication of amyloid fibrils via secondary nucleation is an intriguing
    physicochemical phenomenon in which existing fibrils catalyze the formation of
    their own copies. The molecular events behind this fibril surface-mediated process
    remain largely inaccessible to current structural and imaging techniques. Using
    statistical mechanics, computer modeling, and chemical kinetics, we show that
    the catalytic structure of the fibril surface can be inferred from the aggregation
    behavior in the presence and absence of a fibril-binding inhibitor. We apply our
    approach to the case of Alzheimer’s A\r\n amyloid fibrils formed in the presence
    of proSP-C Brichos inhibitors. We find that self-replication of A\r\n fibrils
    occurs on small catalytic sites on the fibril surface, which are far apart from
    each other, and each of which can be covered by a single Brichos inhibitor."
acknowledgement: We acknowledge support from the Erasmus programme and the University
  College London Institute for the Physics of Living Systems (S.C., T.C.T.M., A.Š.),
  the Biotechnology and Biological Sciences Research Council (T.P.J.K.), the Engineering
  and Physical Sciences Research Council (D.F.), the European Research Council (T.P.J.K.,
  S.L., D.F., and A.Š.), the Frances and Augustus Newman Foundation (T.P.J.K.), the
  Academy of Medical Sciences and Wellcome Trust (A.Š.), and the Royal Society (S.C.
  and A.Š.).
article_number: e2220075121
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Samo
  full_name: Curk, Samo
  id: 031eff0d-d481-11ee-8508-cd12a7a86e5b
  last_name: Curk
  orcid: 0000-0001-6160-9766
- first_name: Johannes
  full_name: Krausser, Johannes
  last_name: Krausser
- first_name: Georg
  full_name: Meisl, Georg
  last_name: Meisl
- first_name: Daan
  full_name: Frenkel, Daan
  last_name: Frenkel
- first_name: Sara
  full_name: Linse, Sara
  last_name: Linse
- first_name: Thomas C.T.
  full_name: Michaels, Thomas C.T.
  last_name: Michaels
- first_name: Tuomas P.J.
  full_name: Knowles, Tuomas P.J.
  last_name: Knowles
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
citation:
  ama: Curk S, Krausser J, Meisl G, et al. Self-replication of Aβ42 aggregates occurs
    on small and isolated fibril sites. <i>Proceedings of the National Academy of
    Sciences of the United States of America</i>. 2024;121(7). doi:<a href="https://doi.org/10.1073/pnas.2220075121">10.1073/pnas.2220075121</a>
  apa: Curk, S., Krausser, J., Meisl, G., Frenkel, D., Linse, S., Michaels, T. C.
    T., … Šarić, A. (2024). Self-replication of Aβ42 aggregates occurs on small and
    isolated fibril sites. <i>Proceedings of the National Academy of Sciences of the
    United States of America</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.2220075121">https://doi.org/10.1073/pnas.2220075121</a>
  chicago: Curk, Samo, Johannes Krausser, Georg Meisl, Daan Frenkel, Sara Linse, Thomas
    C.T. Michaels, Tuomas P.J. Knowles, and Anđela Šarić. “Self-Replication of Aβ42
    Aggregates Occurs on Small and Isolated Fibril Sites.” <i>Proceedings of the National
    Academy of Sciences of the United States of America</i>. National Academy of Sciences,
    2024. <a href="https://doi.org/10.1073/pnas.2220075121">https://doi.org/10.1073/pnas.2220075121</a>.
  ieee: S. Curk <i>et al.</i>, “Self-replication of Aβ42 aggregates occurs on small
    and isolated fibril sites,” <i>Proceedings of the National Academy of Sciences
    of the United States of America</i>, vol. 121, no. 7. National Academy of Sciences,
    2024.
  ista: Curk S, Krausser J, Meisl G, Frenkel D, Linse S, Michaels TCT, Knowles TPJ,
    Šarić A. 2024. Self-replication of Aβ42 aggregates occurs on small and isolated
    fibril sites. Proceedings of the National Academy of Sciences of the United States
    of America. 121(7), e2220075121.
  mla: Curk, Samo, et al. “Self-Replication of Aβ42 Aggregates Occurs on Small and
    Isolated Fibril Sites.” <i>Proceedings of the National Academy of Sciences of
    the United States of America</i>, vol. 121, no. 7, e2220075121, National Academy
    of Sciences, 2024, doi:<a href="https://doi.org/10.1073/pnas.2220075121">10.1073/pnas.2220075121</a>.
  short: S. Curk, J. Krausser, G. Meisl, D. Frenkel, S. Linse, T.C.T. Michaels, T.P.J.
    Knowles, A. Šarić, Proceedings of the National Academy of Sciences of the United
    States of America 121 (2024).
corr_author: '1'
das_tickbox: '1'
dataavailabilitystatement: Aggregation data and the source code for the coarse-grained
  computer model have been deposited in Figshare (https://figshare.com/s/85798bba4ebc68d822ed)
date_created: 2024-02-18T23:01:00Z
date_published: 2024-02-13T00:00:00Z
date_updated: 2026-09-24T10:27:36Z
day: '13'
ddc:
- '570'
department:
- _id: AnSa
doi: 10.1073/pnas.2220075121
ec_funded: 1
external_id:
  isi:
  - '001169063600007'
  pmid:
  - '38335256'
file:
- access_level: open_access
  checksum: 5aeb65bcc0dd829b1f9ab307c5031d4b
  content_type: application/pdf
  creator: dernst
  date_created: 2024-02-26T08:20:00Z
  date_updated: 2024-02-26T08:20:00Z
  file_id: '15026'
  file_name: 2024_PNAS_Curk.pdf
  file_size: 7699487
  relation: main_file
  success: 1
file_date_updated: 2024-02-26T08:20:00Z
fulldoi: https://doi.org/10.1073/pnas.2220075121
has_accepted_license: '1'
intvolume: '       121'
isi: 1
issue: '7'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: eba2549b-77a9-11ec-83b8-a81e493eae4e
  call_identifier: H2020
  grant_number: '802960'
  name: 'Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines'
publication: Proceedings of the National Academy of Sciences of the United States
  of America
publication_identifier:
  eissn:
  - 1091-6490
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
related_material:
  record:
  - id: '15027'
    relation: research_data
    status: public
researchdata_availability: yes
scopus_import: '1'
status: public
supplementarymaterial: no
title: Self-replication of Aβ42 aggregates occurs on small and isolated fibril sites
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 121
year: '2024'
...
---
DOAJ_listed: '1'
_id: '17050'
abstract:
- lang: eng
  text: The process of polymer condensation, i.e., the formation of bonds between
    reactive end groups, is ubiquitous in both industry and biology. Here we study
    generic systems undergoing polymer condensation in competition with cyclization.
    Using a generalized Smoluchowski theory, molecular dynamics simulations and experiments
    with DNA and ATP-consuming T4 ligase, we find that this system displays a transition,
    from a ring-dominated regime with finite-length chains at infinite time to a linear-polymers-dominated
    one with chains that keep growing in time. Finally, we show that fluids prepared
    close to the transition may have widely different compositions and rheology at
    large condensation times.
acknowledgement: D.M. acknowledges the support of the Royal Society via a University
  Research Fellowship. This project has received support from the European Research
  Council (ERC) under the European Union’s Horizon 2020 Research and Innovation Program
  (Grant Agreement No. 947918 to D.M. and No. 677532 to M.L.). The authors acknowledge
  insightful discussions with Daan Noordermeer and Antonio Valdes, who also kindly
  gifted us with the 1288 plasmid.
article_number: '023189'
article_processing_charge: Yes
article_type: original
arxiv: 1
author:
- first_name: Maria
  full_name: Panoukidou, Maria
  last_name: Panoukidou
- first_name: Simon
  full_name: Weir, Simon
  last_name: Weir
- first_name: Valerio
  full_name: Sorichetti, Valerio
  id: ef8a92cb-c7b6-11ec-8bea-e1fd5847bc5b
  last_name: Sorichetti
  orcid: 0000-0002-9645-6576
- first_name: Yair Gutierrez
  full_name: Fosado, Yair Gutierrez
  last_name: Fosado
- first_name: Martin
  full_name: Lenz, Martin
  last_name: Lenz
- first_name: Davide
  full_name: Michieletto, Davide
  last_name: Michieletto
citation:
  ama: Panoukidou M, Weir S, Sorichetti V, Fosado YG, Lenz M, Michieletto D. Runaway
    transition in irreversible polymer condensation with cyclization. <i>Physical
    Review Research</i>. 2024;6(2). doi:<a href="https://doi.org/10.1103/PhysRevResearch.6.023189">10.1103/PhysRevResearch.6.023189</a>
  apa: Panoukidou, M., Weir, S., Sorichetti, V., Fosado, Y. G., Lenz, M., &#38; Michieletto,
    D. (2024). Runaway transition in irreversible polymer condensation with cyclization.
    <i>Physical Review Research</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevResearch.6.023189">https://doi.org/10.1103/PhysRevResearch.6.023189</a>
  chicago: Panoukidou, Maria, Simon Weir, Valerio Sorichetti, Yair Gutierrez Fosado,
    Martin Lenz, and Davide Michieletto. “Runaway Transition in Irreversible Polymer
    Condensation with Cyclization.” <i>Physical Review Research</i>. American Physical
    Society, 2024. <a href="https://doi.org/10.1103/PhysRevResearch.6.023189">https://doi.org/10.1103/PhysRevResearch.6.023189</a>.
  ieee: M. Panoukidou, S. Weir, V. Sorichetti, Y. G. Fosado, M. Lenz, and D. Michieletto,
    “Runaway transition in irreversible polymer condensation with cyclization,” <i>Physical
    Review Research</i>, vol. 6, no. 2. American Physical Society, 2024.
  ista: Panoukidou M, Weir S, Sorichetti V, Fosado YG, Lenz M, Michieletto D. 2024.
    Runaway transition in irreversible polymer condensation with cyclization. Physical
    Review Research. 6(2), 023189.
  mla: Panoukidou, Maria, et al. “Runaway Transition in Irreversible Polymer Condensation
    with Cyclization.” <i>Physical Review Research</i>, vol. 6, no. 2, 023189, American
    Physical Society, 2024, doi:<a href="https://doi.org/10.1103/PhysRevResearch.6.023189">10.1103/PhysRevResearch.6.023189</a>.
  short: M. Panoukidou, S. Weir, V. Sorichetti, Y.G. Fosado, M. Lenz, D. Michieletto,
    Physical Review Research 6 (2024).
das_tickbox: '0'
date_created: 2024-05-26T22:00:58Z
date_published: 2024-05-01T00:00:00Z
date_updated: 2026-09-24T10:26:36Z
day: '01'
ddc:
- '530'
department:
- _id: AnSa
doi: 10.1103/PhysRevResearch.6.023189
external_id:
  arxiv:
  - '2210.14010'
file:
- access_level: open_access
  checksum: 63a962d49ef1e21a3367d265784df14b
  content_type: application/pdf
  creator: dernst
  date_created: 2024-05-27T06:37:01Z
  date_updated: 2024-05-27T06:37:01Z
  file_id: '17055'
  file_name: 2024_PhysicalReviewResearch_Panoukidou.pdf
  file_size: 1409416
  relation: main_file
  success: 1
file_date_updated: 2024-05-27T06:37:01Z
fulldoi: https://doi.org/10.1103/PhysRevResearch.6.023189
has_accepted_license: '1'
intvolume: '         6'
issue: '2'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
publication: Physical Review Research
publication_identifier:
  eissn:
  - 2643-1564
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: no
title: Runaway transition in irreversible polymer condensation with cyclization
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: 6
year: '2024'
...
---
_id: '15116'
abstract:
- lang: eng
  text: Water is known to play an important role in collagen self-assembly, but it
    is still largely unclear how water–collagen interactions influence the assembly
    process and determine the fibril network properties. Here, we use the H2O/D2O
    isotope effect on the hydrogen-bond strength in water to investigate the role
    of hydration in collagen self-assembly. We dissolve collagen in H2O and D2O and
    compare the growth kinetics and the structure of the collagen assemblies formed
    in these water isotopomers. Surprisingly, collagen assembly occurs ten times faster
    in D2O than in H2O, and collagen in D2O self-assembles into much thinner fibrils,
    that form a more inhomogeneous and softer network, with a fourfold reduction in
    elastic modulus when compared to H2O. Combining spectroscopic measurements with
    atomistic simulations, we show that collagen in D2O is less hydrated than in H2O.
    This partial dehydration lowers the enthalpic penalty for water removal and reorganization
    at the collagen–water interface, increasing the self-assembly rate and the number
    of nucleation centers, leading to thinner fibrils and a softer network. Coarse-grained
    simulations show that the acceleration in the initial nucleation rate can be reproduced
    by the enhancement of electrostatic interactions. These results show that water
    acts as a mediator between collagen monomers, by modulating their interactions
    so as to optimize the assembly process and, thus, the final network properties.
    We believe that isotopically modulating the hydration of proteins can be a valuable
    method to investigate the role of water in protein structural dynamics and protein
    self-assembly.
acknowledgement: We thank Dr. Steven Roeters (Aarhus University), Dr. Federica Burla,
  and Prof. Dr. Mischa Bonn (Institute for Polymer Research, Mainz, Germany) for the
  useful discussions. We thank Dr. Wim Roeterdink and Michiel Hilberts for technical
  support. G.H.K. acknowledges financial support by the “BaSyC Building a Synthetic
  Cell” Gravitation grant (024.003.019) of The Netherlands Ministry of Education,
  Culture and Science (OCW) and The Netherlands Organization for Scientific Research
  and from NWO grant OCENW.GROOT.2019.022. This work has received support from the
  National Research Foundation of Korea (NRF), funded by the Ministry of Science and
  ICT, under Grant No. 2022K1A3A1A04062969. This publication is part of the project
  (with Project Number VI.Veni.212.240) of the research programme NWO Talent Programme
  Veni 2021, which is financed by the Dutch Research Council (NWO). I.M.I. acknowledges
  support from the Sectorplan Bèta & Techniek of the Dutch Government and the Dementia
  Research - Synapsis Foundation Switzerland. A.Š. and K.K. acknowledge support from
  Royal Society and European Research Council Starting Grant. G. Giubertoni kindly
  thanks to the Care4Bones community and the Collagen Café community for reminding
  that we do not own the knowledge we create, but it is, rather, a collective resource
  intended for the advancement of human progress.
article_number: e2313162121
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Giulia
  full_name: Giubertoni, Giulia
  last_name: Giubertoni
- first_name: Liru
  full_name: Feng, Liru
  last_name: Feng
- first_name: Kevin
  full_name: Klein, Kevin
  last_name: Klein
- first_name: Guido
  full_name: Giannetti, Guido
  last_name: Giannetti
- first_name: Luco
  full_name: Rutten, Luco
  last_name: Rutten
- first_name: Yeji
  full_name: Choi, Yeji
  last_name: Choi
- first_name: Anouk
  full_name: Van Der Net, Anouk
  last_name: Van Der Net
- first_name: Gerard
  full_name: Castro-Linares, Gerard
  last_name: Castro-Linares
- first_name: Federico
  full_name: Caporaletti, Federico
  last_name: Caporaletti
- first_name: Dimitra
  full_name: Micha, Dimitra
  last_name: Micha
- first_name: Johannes
  full_name: Hunger, Johannes
  last_name: Hunger
- first_name: Antoine
  full_name: Deblais, Antoine
  last_name: Deblais
- first_name: Daniel
  full_name: Bonn, Daniel
  last_name: Bonn
- first_name: Nico
  full_name: Sommerdijk, Nico
  last_name: Sommerdijk
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Ioana M.
  full_name: Ilie, Ioana M.
  last_name: Ilie
- first_name: Gijsje H.
  full_name: Koenderink, Gijsje H.
  last_name: Koenderink
- first_name: Sander
  full_name: Woutersen, Sander
  last_name: Woutersen
citation:
  ama: Giubertoni G, Feng L, Klein K, et al. Elucidating the role of water in collagen
    self-assembly by isotopically modulating collagen hydration. <i>Proceedings of
    the National Academy of Sciences of the United States of America</i>. 2024;121(11).
    doi:<a href="https://doi.org/10.1073/pnas.2313162121">10.1073/pnas.2313162121</a>
  apa: Giubertoni, G., Feng, L., Klein, K., Giannetti, G., Rutten, L., Choi, Y., …
    Woutersen, S. (2024). Elucidating the role of water in collagen self-assembly
    by isotopically modulating collagen hydration. <i>Proceedings of the National
    Academy of Sciences of the United States of America</i>. National Academy of Sciences.
    <a href="https://doi.org/10.1073/pnas.2313162121">https://doi.org/10.1073/pnas.2313162121</a>
  chicago: Giubertoni, Giulia, Liru Feng, Kevin Klein, Guido Giannetti, Luco Rutten,
    Yeji Choi, Anouk Van Der Net, et al. “Elucidating the Role of Water in Collagen
    Self-Assembly by Isotopically Modulating Collagen Hydration.” <i>Proceedings of
    the National Academy of Sciences of the United States of America</i>. National
    Academy of Sciences, 2024. <a href="https://doi.org/10.1073/pnas.2313162121">https://doi.org/10.1073/pnas.2313162121</a>.
  ieee: G. Giubertoni <i>et al.</i>, “Elucidating the role of water in collagen self-assembly
    by isotopically modulating collagen hydration,” <i>Proceedings of the National
    Academy of Sciences of the United States of America</i>, vol. 121, no. 11. National
    Academy of Sciences, 2024.
  ista: Giubertoni G, Feng L, Klein K, Giannetti G, Rutten L, Choi Y, Van Der Net
    A, Castro-Linares G, Caporaletti F, Micha D, Hunger J, Deblais A, Bonn D, Sommerdijk
    N, Šarić A, Ilie IM, Koenderink GH, Woutersen S. 2024. Elucidating the role of
    water in collagen self-assembly by isotopically modulating collagen hydration.
    Proceedings of the National Academy of Sciences of the United States of America.
    121(11), e2313162121.
  mla: Giubertoni, Giulia, et al. “Elucidating the Role of Water in Collagen Self-Assembly
    by Isotopically Modulating Collagen Hydration.” <i>Proceedings of the National
    Academy of Sciences of the United States of America</i>, vol. 121, no. 11, e2313162121,
    National Academy of Sciences, 2024, doi:<a href="https://doi.org/10.1073/pnas.2313162121">10.1073/pnas.2313162121</a>.
  short: G. Giubertoni, L. Feng, K. Klein, G. Giannetti, L. Rutten, Y. Choi, A. Van
    Der Net, G. Castro-Linares, F. Caporaletti, D. Micha, J. Hunger, A. Deblais, D.
    Bonn, N. Sommerdijk, A. Šarić, I.M. Ilie, G.H. Koenderink, S. Woutersen, Proceedings
    of the National Academy of Sciences of the United States of America 121 (2024).
das_tickbox: '1'
dataavailabilitystatement: Turbidity data; IR and 2D-IR data; TEM images; cryo-TEM
  images; CRM images; coarse grained simulations; molecular dynamics simulation data
  have been deposited in UvAauas.figshare 10.21942/uva.24829896
date_created: 2024-03-17T23:00:57Z
date_published: 2024-03-12T00:00:00Z
date_updated: 2026-09-24T10:42:11Z
day: '12'
ddc:
- '550'
department:
- _id: AnSa
doi: 10.1073/pnas.2313162121
external_id:
  isi:
  - '001206387400001'
  pmid:
  - '38451946'
file:
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  date_created: 2024-03-19T10:22:42Z
  date_updated: 2024-03-19T10:22:42Z
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  success: 1
file_date_updated: 2024-03-19T10:22:42Z
fulldoi: https://doi.org/10.1073/pnas.2313162121
has_accepted_license: '1'
intvolume: '       121'
isi: 1
issue: '11'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
publication: Proceedings of the National Academy of Sciences of the United States
  of America
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
related_material:
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    status: public
researchdata_availability: yes
scopus_import: '1'
status: public
supplementarymaterial: no
title: Elucidating the role of water in collagen self-assembly by isotopically modulating
  collagen hydration
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: 121
year: '2024'
...
---
OA_place: publisher
OA_type: hybrid
_id: '18526'
abstract:
- lang: eng
  text: Multivesicular endosomes (MVEs) sequester membrane proteins destined for degradation
    within intralumenal vesicles (ILVs), a process mediated by the membrane-remodeling
    action of Endosomal Sorting Complex Required for Transport (ESCRT) proteins. In
    Arabidopsis, endosomal membrane constriction and scission are uncoupled, resulting
    in the formation of extensive concatenated ILV networks and enhancing cargo sequestration
    efficiency. Here, we used a combination of electron tomography, computer simulations,
    and mathematical modeling to address the questions of when concatenated ILV networks
    evolved in plants and what drives their formation. Through morphometric analyses
    of tomographic reconstructions of endosomes across yeast, algae, and various land
    plants, we have found that ILV concatenation is widespread within plant species,
    but only prevalent in seed plants, especially in flowering plants. Multiple budding
    sites that require the formation of pores in the limiting membrane were only identified
    in hornworts and seed plants, suggesting that this mechanism has evolved independently
    in both plant lineages. To identify the conditions under which these multiple
    budding sites can arise, we used particle-based molecular dynamics simulations
    and found that changes in ESCRT filament properties, such as filament curvature
    and membrane binding energy, can generate the membrane shapes observed in multiple
    budding sites. To understand the relationship between membrane budding activity
    and ILV network topology, we performed computational simulations and identified
    a set of membrane remodeling parameters that can recapitulate our tomographic
    datasets.
acknowledgement: We would like to thank Janice Pennington for her support with electron
  tomography data collection, Dr. Ingrid Jordon-Thaden, director of the Botany Garden
  and Greenhouse of University of Wisconsin Madison, for her invaluable assistance
  collecting plant materials, Dr. Marie Trest for providing Chara specimens, and Dr.
  Nicholas Keuler for his advice on statistical analyses. We thank Charlie Hamilton
  for exploring the initial computational model. This work was supported by grant
  NSF MCB 2114603 and NIH 1S10OD026769-01 to M.S.O. F.F acknowledges support as a
  NOMIS Fellow from the NOMIS Foundation. A.Š. acknowledges ERC Starting Grant “NEPA”
  802960.
article_number: e2409407121
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Ethan
  full_name: Weiner, Ethan
  last_name: Weiner
- first_name: Elizabeth
  full_name: Berryman, Elizabeth
  last_name: Berryman
- first_name: Felix F
  full_name: Frey, Felix F
  id: a0270b37-8f1a-11ec-95c7-8e710c59a4f3
  last_name: Frey
  orcid: 0000-0001-8501-6017
- first_name: Ariadna González
  full_name: Solís, Ariadna González
  last_name: Solís
- first_name: André
  full_name: Leier, André
  last_name: Leier
- first_name: Tatiana Marquez
  full_name: Lago, Tatiana Marquez
  last_name: Lago
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Marisa S.
  full_name: Otegui, Marisa S.
  last_name: Otegui
citation:
  ama: Weiner E, Berryman E, Frey FF, et al. Endosomal membrane budding patterns in
    plants. <i>Proceedings of the National Academy of Sciences of the United States
    of America</i>. 2024;121(44). doi:<a href="https://doi.org/10.1073/pnas.2409407121">10.1073/pnas.2409407121</a>
  apa: Weiner, E., Berryman, E., Frey, F. F., Solís, A. G., Leier, A., Lago, T. M.,
    … Otegui, M. S. (2024). Endosomal membrane budding patterns in plants. <i>Proceedings
    of the National Academy of Sciences of the United States of America</i>. National
    Academy of Sciences. <a href="https://doi.org/10.1073/pnas.2409407121">https://doi.org/10.1073/pnas.2409407121</a>
  chicago: Weiner, Ethan, Elizabeth Berryman, Felix F Frey, Ariadna González Solís,
    André Leier, Tatiana Marquez Lago, Anđela Šarić, and Marisa S. Otegui. “Endosomal
    Membrane Budding Patterns in Plants.” <i>Proceedings of the National Academy of
    Sciences of the United States of America</i>. National Academy of Sciences, 2024.
    <a href="https://doi.org/10.1073/pnas.2409407121">https://doi.org/10.1073/pnas.2409407121</a>.
  ieee: E. Weiner <i>et al.</i>, “Endosomal membrane budding patterns in plants,”
    <i>Proceedings of the National Academy of Sciences of the United States of America</i>,
    vol. 121, no. 44. National Academy of Sciences, 2024.
  ista: Weiner E, Berryman E, Frey FF, Solís AG, Leier A, Lago TM, Šarić A, Otegui
    MS. 2024. Endosomal membrane budding patterns in plants. Proceedings of the National
    Academy of Sciences of the United States of America. 121(44), e2409407121.
  mla: Weiner, Ethan, et al. “Endosomal Membrane Budding Patterns in Plants.” <i>Proceedings
    of the National Academy of Sciences of the United States of America</i>, vol.
    121, no. 44, e2409407121, National Academy of Sciences, 2024, doi:<a href="https://doi.org/10.1073/pnas.2409407121">10.1073/pnas.2409407121</a>.
  short: E. Weiner, E. Berryman, F.F. Frey, A.G. Solís, A. Leier, T.M. Lago, A. Šarić,
    M.S. Otegui, Proceedings of the National Academy of Sciences of the United States
    of America 121 (2024).
das_tickbox: '1'
dataavailabilitystatement: Electron tomogram files are deposited in EMPIAR under EMPIAR-12299
  (54). All other data are included in the manuscript and/or supporting information
date_created: 2024-11-10T23:01:59Z
date_published: 2024-10-29T00:00:00Z
date_updated: 2026-09-24T10:41:24Z
day: '29'
ddc:
- '570'
department:
- _id: AnSa
doi: 10.1073/pnas.2409407121
ec_funded: 1
external_id:
  isi:
  - '001349500800007'
  pmid:
  - '39441629'
file:
- access_level: open_access
  checksum: 21c82d2ab58ff99b2bd0489797be42e5
  content_type: application/pdf
  creator: dernst
  date_created: 2024-11-11T09:35:15Z
  date_updated: 2024-11-11T09:35:15Z
  file_id: '18538'
  file_name: 2024_PNAS_Weiner.pdf
  file_size: 5268074
  relation: main_file
  success: 1
file_date_updated: 2024-11-11T09:35:15Z
fulldoi: https://doi.org/10.1073/pnas.2409407121
has_accepted_license: '1'
intvolume: '       121'
isi: 1
issue: '44'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: eba2549b-77a9-11ec-83b8-a81e493eae4e
  call_identifier: H2020
  grant_number: '802960'
  name: 'Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines'
publication: Proceedings of the National Academy of Sciences of the United States
  of America
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
researchdata_availability: yes
scopus_import: '1'
status: public
supplementarymaterial: yes
title: Endosomal membrane budding patterns in plants
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 121
year: '2024'
...
---
APC_amount: 1530 EUR
OA_place: publisher
OA_type: gold
_id: '15401'
abstract:
- lang: eng
  text: Amide-proton-detected magic-angle-spinning NMR of deuterated proteins has
    become a main technique in NMR-based structural biology. In standard deuteration
    protocols that rely on D2O-based culture media, non-exchangeable amide sites remain
    deuterated, making these sites unobservable. Here we demonstrate that proteins
    produced with a H2O-based culture medium doped with deuterated cell lysate allow
    scientists to overcome this “reprotonation bottleneck” while retaining a high
    level of deuteration (ca. 80 %) and narrow linewidths. We quantified coherence
    lifetimes of several proteins prepared with this labeling pattern over a range
    of magic-angle-spinning (MAS) frequencies (40–100 kHz). We demonstrate that under
    commonly used conditions (50–60 kHz MAS), the amide 1H linewidths with our labeling
    approach are comparable to those of perdeuterated proteins and better than those
    of protonated samples at 100 kHz. For three proteins in the 33–50 kDa size range,
    many previously unobserved amides become visible. We report how to prepare the
    deuterated cell lysate for our approach from fractions of perdeuterated cultures
    which are usually discarded, and we show that such media can be used identically
    to commercial media. The residual protonation of Hα sites allows for well-resolved
    Hα-detected spectra and Hα resonance assignment, exemplified by the de novo assignment
    of 168 Hα sites in a 39 kDa protein. The approach based on this H2O/cell-lysate
    deuteration and MAS frequencies compatible with 1.3 or 1.9 mm rotors presents
    a strong sensitivity benefit over 0.7 mm 100 kHz MAS experiments.
acknowledged_ssus:
- _id: NMR
acknowledgement: "We thank Dominique Madern (IBS Grenoble) for providing the plasmid
  for MalDH and feedback on the article, Alicia Vallet for excellent support at the
  Grenoble NMR facility, and Petra Rovo and Margarita Valhondo at the IST Austria
  NMR Service Unit. We thank Dorothea Anrather in the mass spectrometry facility of
  Max Perutz Labs for the mass spectrometry analysis using the instruments of the
  Vienna BioCenter Core Facilities (VBCF). We are grateful to Jean-Pierre Andrieu
  (Plateforme Seq3A, IBS Grenoble) for the analysis of the amino acid composition
  of the in-house-prepared lysates. We are grateful to Rasmus Linser (Technical University
  Dortmund) for sharing a paper draft describing a similar study. This work was supported
  by the Austrian Science Fund (FWF; project number I5812-B). We thank Tobias Schubeis
  (Lyon) and the reviewers for constructive input.\r\nThis research has been supported
  by the Austrian Science Fund (grant no. I5812-B). Part of this work used the platforms
  of the Grenoble Instruct-ERIC center (ISBG; UAR 3518 CNRS-CEA-UGA-EMBL) within the
  Grenoble Partnership for 40 Structural Biology (PSB), supported by FRISBI (ANR-10-INBS-0005-02)
  and GRAL, financed within the University Grenoble Alpes graduate school (Ecoles
  Universitaires de Recherche) CBH-EUR-GS (ANR-17-EURE-0003). IBS acknowledges integration
  into the Interdisciplinary Research Institute of Grenoble (IRIG, 45 CEA). Charles-Adrien
  Arnaud was funded by GRAL."
article_processing_charge: Yes
article_type: original
author:
- first_name: Federico
  full_name: Napoli, Federico
  id: d42e08e7-f4fc-11eb-af0a-d71e26138f1b
  last_name: Napoli
  orcid: 0000-0002-9043-136X
- first_name: Jia-Ying
  full_name: Guan, Jia-Ying
  last_name: Guan
- first_name: Charles-Adrien
  full_name: Arnaud, Charles-Adrien
  last_name: Arnaud
- first_name: Pavel
  full_name: Macek, Pavel
  last_name: Macek
- first_name: Hugo
  full_name: Fraga, Hugo
  last_name: Fraga
- first_name: Cécile
  full_name: Breyton, Cécile
  last_name: Breyton
- first_name: Paul
  full_name: Schanda, Paul
  id: 7B541462-FAF6-11E9-A490-E8DFE5697425
  last_name: Schanda
  orcid: 0000-0002-9350-7606
citation:
  ama: 'Napoli F, Guan J-Y, Arnaud C-A, et al. Deuteration of proteins boosted by
    cell lysates: High-resolution amide and Ha magic-angle-spinning (MAS) NMR without
    the reprotonation bottleneck. <i>Magnetic Resonance</i>. 2024;5(1):33-49. doi:<a
    href="https://doi.org/10.5194/mr-5-33-2024">10.5194/mr-5-33-2024</a>'
  apa: 'Napoli, F., Guan, J.-Y., Arnaud, C.-A., Macek, P., Fraga, H., Breyton, C.,
    &#38; Schanda, P. (2024). Deuteration of proteins boosted by cell lysates: High-resolution
    amide and Ha magic-angle-spinning (MAS) NMR without the reprotonation bottleneck.
    <i>Magnetic Resonance</i>. Copernicus Publications. <a href="https://doi.org/10.5194/mr-5-33-2024">https://doi.org/10.5194/mr-5-33-2024</a>'
  chicago: 'Napoli, Federico, Jia-Ying Guan, Charles-Adrien Arnaud, Pavel Macek, Hugo
    Fraga, Cécile Breyton, and Paul Schanda. “Deuteration of Proteins Boosted by Cell
    Lysates: High-Resolution Amide and Ha Magic-Angle-Spinning (MAS) NMR without the
    Reprotonation Bottleneck.” <i>Magnetic Resonance</i>. Copernicus Publications,
    2024. <a href="https://doi.org/10.5194/mr-5-33-2024">https://doi.org/10.5194/mr-5-33-2024</a>.'
  ieee: 'F. Napoli <i>et al.</i>, “Deuteration of proteins boosted by cell lysates:
    High-resolution amide and Ha magic-angle-spinning (MAS) NMR without the reprotonation
    bottleneck,” <i>Magnetic Resonance</i>, vol. 5, no. 1. Copernicus Publications,
    pp. 33–49, 2024.'
  ista: 'Napoli F, Guan J-Y, Arnaud C-A, Macek P, Fraga H, Breyton C, Schanda P. 2024.
    Deuteration of proteins boosted by cell lysates: High-resolution amide and Ha
    magic-angle-spinning (MAS) NMR without the reprotonation bottleneck. Magnetic
    Resonance. 5(1), 33–49.'
  mla: 'Napoli, Federico, et al. “Deuteration of Proteins Boosted by Cell Lysates:
    High-Resolution Amide and Ha Magic-Angle-Spinning (MAS) NMR without the Reprotonation
    Bottleneck.” <i>Magnetic Resonance</i>, vol. 5, no. 1, Copernicus Publications,
    2024, pp. 33–49, doi:<a href="https://doi.org/10.5194/mr-5-33-2024">10.5194/mr-5-33-2024</a>.'
  short: F. Napoli, J.-Y. Guan, C.-A. Arnaud, P. Macek, H. Fraga, C. Breyton, P. Schanda,
    Magnetic Resonance 5 (2024) 33–49.
corr_author: '1'
date_created: 2024-05-16T15:02:43Z
date_published: 2024-04-19T00:00:00Z
date_updated: 2026-09-24T10:36:36Z
day: '19'
ddc:
- '530'
department:
- _id: PaSc
doi: 10.5194/mr-5-33-2024
external_id:
  pmid:
  - '40384771'
file:
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  creator: dernst
  date_created: 2024-05-22T07:01:15Z
  date_updated: 2024-05-22T07:01:15Z
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  file_name: 2024_MagneticResonance_Napoli.pdf
  file_size: 6657865
  relation: main_file
  success: 1
file_date_updated: 2024-05-22T07:01:15Z
fulldoi: https://doi.org/10.5194/mr-5-33-2024
has_accepted_license: '1'
intvolume: '         5'
issue: '1'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 33-49
pmid: 1
project:
- _id: eb9c82eb-77a9-11ec-83b8-aadd536561cf
  grant_number: I05812
  name: AlloSpace. The emergence and mechanisms of allostery
- _id: 3AC91DDA-15DF-11EA-824D-93A3E7B544D1
  call_identifier: FWF
  name: FWF Open Access Fund
publication: Magnetic Resonance
publication_identifier:
  issn:
  - 2699-0016
publication_status: published
publisher: Copernicus Publications
quality_controlled: '1'
related_material:
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scopus_import: '1'
status: public
title: 'Deuteration of proteins boosted by cell lysates: High-resolution amide and
  Ha magic-angle-spinning (MAS) NMR without the reprotonation bottleneck'
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: 5
year: '2024'
...
---
_id: '18072'
abstract:
- lang: eng
  text: The individualization of chromosomes during early mitosis and their clustering
    upon exit from cell division are two key transitions that ensure efficient segregation
    of eukaryotic chromosomes. Both processes are regulated by the surfactant-like
    protein Ki-67, but how Ki-67 achieves these diametric functions has remained unknown.
    Here, we report that Ki-67 radically switches from a chromosome repellent to a
    chromosome attractant during anaphase in human cells. We show that Ki-67 dephosphorylation
    during mitotic exit and the simultaneous exposure of a conserved basic patch induce
    the RNA-dependent formation of a liquid-like condensed phase on the chromosome
    surface. Experiments and coarse-grained simulations support a model in which the
    coalescence of chromosome surfaces, driven by co-condensation of Ki-67 and RNA,
    promotes clustering of chromosomes. Our study reveals how the switch of Ki-67
    from a surfactant to a liquid-like condensed phase can generate mechanical forces
    during genome segregation that are required for re-establishing nuclear-cytoplasmic
    compartmentalization after mitosis.
acknowledgement: We thank Daniel W. Gerlich for providing cell lines, the EMBL Advanced
  Light Microscopy Facility (ALMF) for support, Christian H. Haering and Thomas Quail
  for input on the manuscript, and Martina Dees for cloning several Ki-67 constructs.
  This work was supported by the German Research Foundation (DFG project number 402723784)
  and the Human Frontier Science Program (CDA00045/2019). A.H.-A. and A.B. have received
  PhD fellowships from the Boehringer Ingelheim Fonds, V.S. and A.Š. were supported
  by the European Research Council (ERC) under the European Union’s Horizon 2020 research
  and innovation programme (grant no. 802960), and Y.H. was supported by a fellowship
  from the EMBL interdisciplinary Postdoc (EIPOD) program (Marie Sklodowska-Curie
  Actions, COFUND grant agreement 664726).
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Alberto
  full_name: Hernandez-Armendariz, Alberto
  last_name: Hernandez-Armendariz
- first_name: Valerio
  full_name: Sorichetti, Valerio
  id: ef8a92cb-c7b6-11ec-8bea-e1fd5847bc5b
  last_name: Sorichetti
  orcid: 0000-0002-9645-6576
- first_name: Yuki
  full_name: Hayashi, Yuki
  last_name: Hayashi
- first_name: Zuzana
  full_name: Koskova, Zuzana
  last_name: Koskova
- first_name: Andreas
  full_name: Brunner, Andreas
  last_name: Brunner
- first_name: Jan
  full_name: Ellenberg, Jan
  last_name: Ellenberg
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Sara
  full_name: Cuylen-Haering, Sara
  last_name: Cuylen-Haering
citation:
  ama: Hernandez-Armendariz A, Sorichetti V, Hayashi Y, et al. A liquid-like coat
    mediates chromosome clustering during mitotic exit. <i>Molecular Cell</i>. 2024;84(17):P3254-3270.E9.
    doi:<a href="https://doi.org/10.1016/j.molcel.2024.07.022">10.1016/j.molcel.2024.07.022</a>
  apa: Hernandez-Armendariz, A., Sorichetti, V., Hayashi, Y., Koskova, Z., Brunner,
    A., Ellenberg, J., … Cuylen-Haering, S. (2024). A liquid-like coat mediates chromosome
    clustering during mitotic exit. <i>Molecular Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.molcel.2024.07.022">https://doi.org/10.1016/j.molcel.2024.07.022</a>
  chicago: Hernandez-Armendariz, Alberto, Valerio Sorichetti, Yuki Hayashi, Zuzana
    Koskova, Andreas Brunner, Jan Ellenberg, Anđela Šarić, and Sara Cuylen-Haering.
    “A Liquid-like Coat Mediates Chromosome Clustering during Mitotic Exit.” <i>Molecular
    Cell</i>. Cell Press, 2024. <a href="https://doi.org/10.1016/j.molcel.2024.07.022">https://doi.org/10.1016/j.molcel.2024.07.022</a>.
  ieee: A. Hernandez-Armendariz <i>et al.</i>, “A liquid-like coat mediates chromosome
    clustering during mitotic exit,” <i>Molecular Cell</i>, vol. 84, no. 17. Cell
    Press, p. P3254–3270.E9, 2024.
  ista: Hernandez-Armendariz A, Sorichetti V, Hayashi Y, Koskova Z, Brunner A, Ellenberg
    J, Šarić A, Cuylen-Haering S. 2024. A liquid-like coat mediates chromosome clustering
    during mitotic exit. Molecular Cell. 84(17), P3254–3270.E9.
  mla: Hernandez-Armendariz, Alberto, et al. “A Liquid-like Coat Mediates Chromosome
    Clustering during Mitotic Exit.” <i>Molecular Cell</i>, vol. 84, no. 17, Cell
    Press, 2024, p. P3254–3270.E9, doi:<a href="https://doi.org/10.1016/j.molcel.2024.07.022">10.1016/j.molcel.2024.07.022</a>.
  short: A. Hernandez-Armendariz, V. Sorichetti, Y. Hayashi, Z. Koskova, A. Brunner,
    J. Ellenberg, A. Šarić, S. Cuylen-Haering, Molecular Cell 84 (2024) P3254–3270.E9.
das_tickbox: '1'
dataavailabilitystatement: 'Raw image files of all figures have been deposited at
  Mendeley Data and are publicly available as of the date of publication (Mendeley
  data: https://doi.org/10.17632/dwcpnncsyd.1). All other data reported in this paper
  will be shared by the lead contact upon request'
date_created: 2024-09-15T22:01:41Z
date_published: 2024-09-05T00:00:00Z
date_updated: 2026-09-24T10:43:18Z
day: '05'
ddc:
- '570'
department:
- _id: AnSa
doi: 10.1016/j.molcel.2024.07.022
ec_funded: 1
external_id:
  isi:
  - '001309051100001'
  pmid:
  - '39153474'
file:
- access_level: open_access
  checksum: 3f360e0287b8ec79fb2b8b02b5070360
  content_type: application/pdf
  creator: dernst
  date_created: 2024-09-16T07:38:38Z
  date_updated: 2024-09-16T07:38:38Z
  file_id: '18075'
  file_name: 2024_MolecularCell_HernandezArmendariz.pdf
  file_size: 11654644
  relation: main_file
  success: 1
file_date_updated: 2024-09-16T07:38:38Z
fulldoi: https://doi.org/10.1016/j.molcel.2024.07.022
has_accepted_license: '1'
intvolume: '        84'
isi: 1
issue: '17'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: P3254-3270.E9
pmid: 1
project:
- _id: eba2549b-77a9-11ec-83b8-a81e493eae4e
  call_identifier: H2020
  grant_number: '802960'
  name: 'Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines'
publication: Molecular Cell
publication_identifier:
  eissn:
  - 1097-4164
  issn:
  - 1097-2765
publication_status: published
publisher: Cell Press
quality_controlled: '1'
related_material:
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    relation: research_data
    status: public
researchdata_availability: yes
scopus_import: '1'
status: public
supplementarymaterial: yes
title: A liquid-like coat mediates chromosome clustering during mitotic exit
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: 84
year: '2024'
...
---
OA_place: publisher
OA_type: hybrid
_id: '17239'
abstract:
- lang: eng
  text: Collagen is the most abundant protein in tissue scaffolds in live organisms.
    Collagen can self-assemble in vitro, which has led to a number of biotechnological
    and biomedical applications. To understand the dominant factors that participate
    in the formation of collagen nanostructures, here we study in real time and with
    nanoscale resolution the disassembly and reassembly of collagens. We implement
    a high-speed force microscope, which provides in situ high spatiotemporal resolution
    images of collagen nanostructures under changing pH conditions. The disassembly
    and reassembly are dominated by the electrostatic interactions among amino-acid
    residues of different molecules. Acidic conditions favor disassembly by neutralizing
    negatively charged residues. The process sets a net repulsive force between collagen
    molecules. A neutral pH favors the presence of negative and positively charged
    residues along the collagen molecules, which promotes their electrostatic attraction.
    Molecular dynamics simulations reproduce the experimental behavior and validate
    the electrostatic-based model of the disassembly and reassembly processes.
acknowledgement: We are grateful to Nancy Forde (Simon Fraser University) for her
  motivating comments. Financial support from the Ministerio de Ciencia, Innovación
  y Universidades (PID2019-106801GB-I00 and PID2022-136851NB-I00) is acknowledged.
  A.Š. and K.K. acknowledge support from the Royal Society University Research Fellowship
  and ERC the European Union’s Horizon 2020584 Research and Innovation Programme (Grant
  No. 585 80296).
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Clara
  full_name: Garcia-Sacristan, Clara
  last_name: Garcia-Sacristan
- first_name: Victor G.
  full_name: Gisbert, Victor G.
  last_name: Gisbert
- first_name: Kevin
  full_name: Klein, Kevin
  id: 1e7ede04-9e54-11f0-9ec4-8d4d5563c398
  last_name: Klein
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Ricardo
  full_name: Garcia, Ricardo
  last_name: Garcia
citation:
  ama: Garcia-Sacristan C, Gisbert VG, Klein K, Šarić A, Garcia R. In operando imaging
    electrostatic-driven disassembly and reassembly of collagen nanostructures. <i>ACS
    Nano</i>. 2024;18(28):18485-18492. doi:<a href="https://doi.org/10.1021/acsnano.4c03839">10.1021/acsnano.4c03839</a>
  apa: Garcia-Sacristan, C., Gisbert, V. G., Klein, K., Šarić, A., &#38; Garcia, R.
    (2024). In operando imaging electrostatic-driven disassembly and reassembly of
    collagen nanostructures. <i>ACS Nano</i>. American Chemical Society. <a href="https://doi.org/10.1021/acsnano.4c03839">https://doi.org/10.1021/acsnano.4c03839</a>
  chicago: Garcia-Sacristan, Clara, Victor G. Gisbert, Kevin Klein, Anđela Šarić,
    and Ricardo Garcia. “In Operando Imaging Electrostatic-Driven Disassembly and
    Reassembly of Collagen Nanostructures.” <i>ACS Nano</i>. American Chemical Society,
    2024. <a href="https://doi.org/10.1021/acsnano.4c03839">https://doi.org/10.1021/acsnano.4c03839</a>.
  ieee: C. Garcia-Sacristan, V. G. Gisbert, K. Klein, A. Šarić, and R. Garcia, “In
    operando imaging electrostatic-driven disassembly and reassembly of collagen nanostructures,”
    <i>ACS Nano</i>, vol. 18, no. 28. American Chemical Society, pp. 18485–18492,
    2024.
  ista: Garcia-Sacristan C, Gisbert VG, Klein K, Šarić A, Garcia R. 2024. In operando
    imaging electrostatic-driven disassembly and reassembly of collagen nanostructures.
    ACS Nano. 18(28), 18485–18492.
  mla: Garcia-Sacristan, Clara, et al. “In Operando Imaging Electrostatic-Driven Disassembly
    and Reassembly of Collagen Nanostructures.” <i>ACS Nano</i>, vol. 18, no. 28,
    American Chemical Society, 2024, pp. 18485–92, doi:<a href="https://doi.org/10.1021/acsnano.4c03839">10.1021/acsnano.4c03839</a>.
  short: C. Garcia-Sacristan, V.G. Gisbert, K. Klein, A. Šarić, R. Garcia, ACS Nano
    18 (2024) 18485–18492.
das_tickbox: '0'
date_created: 2024-07-14T22:01:12Z
date_published: 2024-07-16T00:00:00Z
date_updated: 2026-09-24T10:43:56Z
day: '16'
ddc:
- '540'
department:
- _id: AnSa
doi: 10.1021/acsnano.4c03839
ec_funded: 1
external_id:
  isi:
  - '001263155500001'
  pmid:
  - '38958189'
file:
- access_level: open_access
  checksum: b7e9ce718e92f568bcb3810e8e28e458
  content_type: application/pdf
  creator: dernst
  date_created: 2025-01-09T12:06:48Z
  date_updated: 2025-01-09T12:06:48Z
  file_id: '18808'
  file_name: 2024_ACSNano_GarciaSacristan.pdf
  file_size: 10036838
  relation: main_file
  success: 1
file_date_updated: 2025-01-09T12:06:48Z
fulldoi: https://doi.org/10.1021/acsnano.4c03839
has_accepted_license: '1'
intvolume: '        18'
isi: 1
issue: '28'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 18485-18492
pmid: 1
project:
- _id: eba2549b-77a9-11ec-83b8-a81e493eae4e
  call_identifier: H2020
  grant_number: '802960'
  name: 'Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines'
publication: ACS Nano
publication_identifier:
  eissn:
  - 1936-086X
  issn:
  - 1936-0851
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: yes
title: In operando imaging electrostatic-driven disassembly and reassembly of collagen
  nanostructures
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: 18
year: '2024'
...
---
OA_place: repository
OA_type: green
_id: '18704'
abstract:
- lang: eng
  text: Clathrin-mediated endocytosis is the main pathway used by eukaryotic cells
    to take up extracellular material, but the dominant physical mechanisms driving
    this process are still elusive. Recently, several high-resolution imaging techniques
    have been used on different cell lines to measure the geometrical properties of
    clathrin-coated pits over their whole lifetime. Here, we first show that the combination
    of all datasets with the recently introduced cooperative curvature model defines
    a consensus pathway, which is characterized by a flat-to-curved transition at
    finite area, followed by linear growth and subsequent saturation of curvature.
    We then apply an energetic model for the composite of the plasma membrane and
    clathrin coat to this consensus pathway to show that the dominant mechanism for
    invagination could be coat stiffening, which might originate from cooperative
    interactions between the different clathrin molecules and progressively drives
    the system toward its intrinsic curvature. Our theory predicts that two length
    scales determine the invagination pathway, namely the patch size at which the
    flat-to-curved transition occurs and the final pit radius.
acknowledgement: We thank Markus Mund, Aline Tschanz, and Jonas Ries for helpful discussions
  and a critical reading of the manuscript. We also kindly acknowledge Simon Scheuring
  for providing the HS-AFM data for the analysis of clathrin coat invagination. We
  thank the reviewers of previous versions of this manuscript for useful feedback
  that helped us to improve this work. F.F. acknowledges financial support by the
  NOMIS foundation. U.S.S. was supported by the Deutsche Forschungsgemeinschaft (DFG,
  German Research Foundation) under Project No. 240245660 (SFB 1129). Moreover, he
  is a member of the Interdisciplinary Center for Scientific Computing (IWR) at Heidelberg
  and of the Max Planck School Matter to Life supported by the German Federal Ministry
  of Education and Research (BMBF) in collaboration with the Max Planck Society.
article_number: '064403'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Felix F
  full_name: Frey, Felix F
  id: a0270b37-8f1a-11ec-95c7-8e710c59a4f3
  last_name: Frey
  orcid: 0000-0001-8501-6017
- first_name: Ulrich S.
  full_name: Schwarz, Ulrich S.
  last_name: Schwarz
citation:
  ama: Frey FF, Schwarz US. Coat stiffening can explain invagination of clathrin-coated
    membranes. <i>Physical Review E</i>. 2024;110(6). doi:<a href="https://doi.org/10.1103/PhysRevE.110.064403">10.1103/PhysRevE.110.064403</a>
  apa: Frey, F. F., &#38; Schwarz, U. S. (2024). Coat stiffening can explain invagination
    of clathrin-coated membranes. <i>Physical Review E</i>. American Physical Society.
    <a href="https://doi.org/10.1103/PhysRevE.110.064403">https://doi.org/10.1103/PhysRevE.110.064403</a>
  chicago: Frey, Felix F, and Ulrich S. Schwarz. “Coat Stiffening Can Explain Invagination
    of Clathrin-Coated Membranes.” <i>Physical Review E</i>. American Physical Society,
    2024. <a href="https://doi.org/10.1103/PhysRevE.110.064403">https://doi.org/10.1103/PhysRevE.110.064403</a>.
  ieee: F. F. Frey and U. S. Schwarz, “Coat stiffening can explain invagination of
    clathrin-coated membranes,” <i>Physical Review E</i>, vol. 110, no. 6. American
    Physical Society, 2024.
  ista: Frey FF, Schwarz US. 2024. Coat stiffening can explain invagination of clathrin-coated
    membranes. Physical Review E. 110(6), 064403.
  mla: Frey, Felix F., and Ulrich S. Schwarz. “Coat Stiffening Can Explain Invagination
    of Clathrin-Coated Membranes.” <i>Physical Review E</i>, vol. 110, no. 6, 064403,
    American Physical Society, 2024, doi:<a href="https://doi.org/10.1103/PhysRevE.110.064403">10.1103/PhysRevE.110.064403</a>.
  short: F.F. Frey, U.S. Schwarz, Physical Review E 110 (2024).
das_tickbox: '0'
date_created: 2024-12-22T23:01:48Z
date_published: 2024-12-10T00:00:00Z
date_updated: 2026-09-24T10:43:36Z
day: '10'
department:
- _id: AnSa
doi: 10.1103/PhysRevE.110.064403
external_id:
  arxiv:
  - '2405.02820'
  isi:
  - '001379135100004'
  pmid:
  - '39916158'
fulldoi: https://doi.org/10.1103/PhysRevE.110.064403
intvolume: '       110'
isi: 1
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2405.02820
month: '12'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review E
publication_identifier:
  eissn:
  - 2470-0053
  issn:
  - 2470-0045
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: no
title: Coat stiffening can explain invagination of clathrin-coated membranes
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 110
year: '2024'
...
---
OA_place: repository
OA_type: green
_id: '22987'
abstract:
- lang: eng
  text: 'Imaging data of all main and supplementary figures. The files are the raw
    microcopy files including all Z-slices and timepoints. '
article_processing_charge: No
author:
- first_name: Alberto
  full_name: Hernandez-Armendariz, Alberto
  last_name: Hernandez-Armendariz
- first_name: Sara
  full_name: Cuylen-Haering, Sara
  last_name: Cuylen-Haering
citation:
  ama: Hernandez-Armendariz A, Cuylen-Haering S. A liquid-like coat mediates chromosome
    clustering during mitotic exit. Hernandez-Armendariz et al. 2024. doi:<a href="https://doi.org/10.17632/dwcpnncsyd.1">10.17632/dwcpnncsyd.1</a>
  apa: Hernandez-Armendariz, A., &#38; Cuylen-Haering, S. (2024). A liquid-like coat
    mediates chromosome clustering during mitotic exit. Hernandez-Armendariz et al.
    Repository. <a href="https://doi.org/10.17632/dwcpnncsyd.1">https://doi.org/10.17632/dwcpnncsyd.1</a>
  chicago: Hernandez-Armendariz, Alberto, and Sara Cuylen-Haering. “A Liquid-like
    Coat Mediates Chromosome Clustering during Mitotic Exit. Hernandez-Armendariz
    et Al.” Repository, 2024. <a href="https://doi.org/10.17632/dwcpnncsyd.1">https://doi.org/10.17632/dwcpnncsyd.1</a>.
  ieee: A. Hernandez-Armendariz and S. Cuylen-Haering, “A liquid-like coat mediates
    chromosome clustering during mitotic exit. Hernandez-Armendariz et al.” Repository,
    2024.
  ista: Hernandez-Armendariz A, Cuylen-Haering S. 2024. A liquid-like coat mediates
    chromosome clustering during mitotic exit. Hernandez-Armendariz et al., Repository,
    <a href="https://doi.org/10.17632/dwcpnncsyd.1">10.17632/dwcpnncsyd.1</a>.
  mla: Hernandez-Armendariz, Alberto, and Sara Cuylen-Haering. <i>A Liquid-like Coat
    Mediates Chromosome Clustering during Mitotic Exit. Hernandez-Armendariz et Al.</i>
    Repository, 2024, doi:<a href="https://doi.org/10.17632/dwcpnncsyd.1">10.17632/dwcpnncsyd.1</a>.
  short: A. Hernandez-Armendariz, S. Cuylen-Haering, (2024).
date_created: 2026-09-24T10:38:23Z
date_published: 2024-08-22T00:00:00Z
date_updated: 2026-09-24T10:43:18Z
day: '22'
ddc:
- '570'
department:
- _id: AnSa
doi: 10.17632/dwcpnncsyd.1
fulldoi: https://doi.org/10.17632/dwcpnncsyd.1
main_file_link:
- open_access: '1'
  url: https://doi.org/10.17632/dwcpnncsyd.1
month: '08'
oa: 1
oa_version: None
publisher: Repository
related_material:
  record:
  - id: '18072'
    relation: used_in_publication
    status: public
status: public
title: A liquid-like coat mediates chromosome clustering during mitotic exit. Hernandez-Armendariz
  et al.
type: research_data_reference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
year: '2024'
...
---
OA_place: repository
OA_type: green
_id: '22940'
article_processing_charge: No
author:
- first_name: Astrid
  full_name: ' Sivertsen, Astrid'
  last_name: ' Sivertsen'
- first_name: Federico
  full_name: Napoli, Federico
  last_name: Napoli
- first_name: Paul
  full_name: Schanda, Paul
  last_name: Schanda
citation:
  ama: Sivertsen A, Napoli F, Schanda P. Amide and a-hydrogens extension to the Solid-state
    NMR assignment of P. horikoshii TET2. 2024. doi:<a href="https://doi.org/10.13018/BMR52400">10.13018/BMR52400</a>
  apa: Sivertsen, A., Napoli, F., &#38; Schanda, P. (2024). Amide and a-hydrogens
    extension to the Solid-state NMR assignment of P. horikoshii TET2. Repository.
    <a href="https://doi.org/10.13018/BMR52400">https://doi.org/10.13018/BMR52400</a>
  chicago: Sivertsen, Astrid, Federico Napoli, and Paul Schanda. “Amide and A-Hydrogens
    Extension to the Solid-State NMR Assignment of P. Horikoshii TET2.” Repository,
    2024. <a href="https://doi.org/10.13018/BMR52400">https://doi.org/10.13018/BMR52400</a>.
  ieee: A.  Sivertsen, F. Napoli, and P. Schanda, “Amide and a-hydrogens extension
    to the Solid-state NMR assignment of P. horikoshii TET2.” Repository, 2024.
  ista: Sivertsen A, Napoli F, Schanda P. 2024. Amide and a-hydrogens extension to
    the Solid-state NMR assignment of P. horikoshii TET2, Repository, <a href="https://doi.org/10.13018/BMR52400">10.13018/BMR52400</a>.
  mla: Sivertsen, Astrid, et al. <i>Amide and A-Hydrogens Extension to the Solid-State
    NMR Assignment of P. Horikoshii TET2</i>. Repository, 2024, doi:<a href="https://doi.org/10.13018/BMR52400">10.13018/BMR52400</a>.
  short: A.  Sivertsen, F. Napoli, P. Schanda, (2024).
date_created: 2026-09-17T09:10:45Z
date_published: 2024-05-15T00:00:00Z
date_updated: 2026-09-24T10:36:36Z
day: '15'
ddc:
- '530'
department:
- _id: PaSc
doi: 10.13018/BMR52400
fulldoi: https://doi.org/10.13018/BMR52400
main_file_link:
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  url: https://doi.org/10.13018/BMR52400
month: '05'
oa: 1
oa_version: None
publisher: Repository
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status: public
title: Amide and a-hydrogens extension to the Solid-state NMR assignment of P. horikoshii
  TET2
type: research_data_reference
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year: '2024'
...
---
_id: '15126'
abstract:
- lang: eng
  text: This zip file contains data, and analysis for the paper "Elucidating the role
    of water in collagen self-assembly by isotopically modulating collagen hydration".
article_processing_charge: No
author:
- first_name: G.
  full_name: Giubertoni, G.
  last_name: Giubertoni
- first_name: S.
  full_name: Woutersen, S.
  last_name: Woutersen
citation:
  ama: Giubertoni G, Woutersen S. Dataset Collagen Self Assembly in H2O and D2O. 2024.
    doi:<a href="https://doi.org/10.21942/UVA.24829896">10.21942/UVA.24829896</a>
  apa: Giubertoni, G., &#38; Woutersen, S. (2024). Dataset Collagen Self Assembly
    in H2O and D2O. Figshare. <a href="https://doi.org/10.21942/UVA.24829896">https://doi.org/10.21942/UVA.24829896</a>
  chicago: Giubertoni, G., and S. Woutersen. “Dataset Collagen Self Assembly in H2O
    and D2O.” Figshare, 2024. <a href="https://doi.org/10.21942/UVA.24829896">https://doi.org/10.21942/UVA.24829896</a>.
  ieee: G. Giubertoni and S. Woutersen, “Dataset Collagen Self Assembly in H2O and
    D2O.” Figshare, 2024.
  ista: Giubertoni G, Woutersen S. 2024. Dataset Collagen Self Assembly in H2O and
    D2O, Figshare, <a href="https://doi.org/10.21942/UVA.24829896">10.21942/UVA.24829896</a>.
  mla: Giubertoni, G., and S. Woutersen. <i>Dataset Collagen Self Assembly in H2O
    and D2O</i>. Figshare, 2024, doi:<a href="https://doi.org/10.21942/UVA.24829896">10.21942/UVA.24829896</a>.
  short: G. Giubertoni, S. Woutersen, (2024).
date_created: 2024-03-19T10:47:16Z
date_published: 2024-02-14T00:00:00Z
date_updated: 2026-09-24T10:42:12Z
day: '14'
ddc:
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fulldoi: https://doi.org/10.21942/UVA.24829896
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main_file_link:
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month: '02'
oa: 1
oa_version: Published Version
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status: public
title: Dataset Collagen Self Assembly in H2O and D2O
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: research_data_reference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
year: '2024'
...
---
_id: '17374'
abstract:
- lang: eng
  text: Achieving photorealistic 3D view synthesis and relighting of human portraits
    is pivotal for advancing AR/VR applications. Existing methodologies in portrait
    relighting demonstrate substantial limitations in terms of generalization and
    3D consistency, coupled with inaccuracies in physically realistic lighting and
    identity preservation. Furthermore, personalization from a single view is difficult
    to achieve and often requires multiview images during the testing phase or involves
    slow optimization processes. This paper introduces Lite2Relight , a novel technique
    that can predict 3D consistent head poses of portraits while performing physically
    plausible light editing at interactive speed. Our method uniquely extends the
    generative capabilities and efficient volumetric representation of EG3D, leveraging
    a lightstage dataset to implicitly disentangle face reflectance and perform relighting
    under target HDRI environment maps. By utilizing a pre-trained geometry-aware
    encoder and a feature alignment module, we map input images into a relightable
    3D space, enhancing them with a strong face geometry and reflectance prior. Through
    extensive quantitative and qualitative evaluations, we show that our method outperforms
    the state-of-the-art methods in terms of efficacy, photorealism, and practical
    application. This includes producing 3D-consistent results of the full head, including
    hair, eyes, and expressions. Lite2Relight paves the way for large-scale adoption
    of photorealistic portrait editing in various domains, offering a robust, interactive
    solution to a previously constrained problem.
acknowledgement: This work was supported by the ERC Consolidator Grant 4DReply (770784).
  We extend our gratitude to Shrisha Bharadwaj for providing feedback and constant
  support.
article_number: '41'
article_processing_charge: Yes (in subscription journal)
arxiv: 1
author:
- first_name: Pramod
  full_name: Rao, Pramod
  last_name: Rao
- first_name: Gereon
  full_name: Fox, Gereon
  last_name: Fox
- first_name: Abhimitra
  full_name: Meka, Abhimitra
  last_name: Meka
- first_name: B. R.
  full_name: Mallikarjun, B. R.
  last_name: Mallikarjun
- first_name: Fangneng
  full_name: Zhan, Fangneng
  last_name: Zhan
- first_name: Tim
  full_name: Weyrich, Tim
  last_name: Weyrich
- first_name: Bernd
  full_name: Bickel, Bernd
  id: 49876194-F248-11E8-B48F-1D18A9856A87
  last_name: Bickel
  orcid: 0000-0001-6511-9385
- first_name: Hanspeter
  full_name: Pfister, Hanspeter
  last_name: Pfister
- first_name: Wojciech
  full_name: Matusik, Wojciech
  last_name: Matusik
- first_name: Mohamed
  full_name: Elgharib, Mohamed
  last_name: Elgharib
- first_name: Christian
  full_name: Theobalt, Christian
  last_name: Theobalt
citation:
  ama: 'Rao P, Fox G, Meka A, et al. Lite2Relight: 3D-aware single image portrait
    relighting. In: <i>Proceedings - SIGGRAPH 2024 Conference Papers</i>. Association
    for Computing Machinery; 2024. doi:<a href="https://doi.org/10.1145/3641519.3657470">10.1145/3641519.3657470</a>'
  apa: 'Rao, P., Fox, G., Meka, A., Mallikarjun, B. R., Zhan, F., Weyrich, T., … Theobalt,
    C. (2024). Lite2Relight: 3D-aware single image portrait relighting. In <i>Proceedings
    - SIGGRAPH 2024 Conference Papers</i>. Denver, CO, United States: Association
    for Computing Machinery. <a href="https://doi.org/10.1145/3641519.3657470">https://doi.org/10.1145/3641519.3657470</a>'
  chicago: 'Rao, Pramod, Gereon Fox, Abhimitra Meka, B. R. Mallikarjun, Fangneng Zhan,
    Tim Weyrich, Bernd Bickel, et al. “Lite2Relight: 3D-Aware Single Image Portrait
    Relighting.” In <i>Proceedings - SIGGRAPH 2024 Conference Papers</i>. Association
    for Computing Machinery, 2024. <a href="https://doi.org/10.1145/3641519.3657470">https://doi.org/10.1145/3641519.3657470</a>.'
  ieee: 'P. Rao <i>et al.</i>, “Lite2Relight: 3D-aware single image portrait relighting,”
    in <i>Proceedings - SIGGRAPH 2024 Conference Papers</i>, Denver, CO, United States,
    2024.'
  ista: 'Rao P, Fox G, Meka A, Mallikarjun BR, Zhan F, Weyrich T, Bickel B, Pfister
    H, Matusik W, Elgharib M, Theobalt C. 2024. Lite2Relight: 3D-aware single image
    portrait relighting. Proceedings - SIGGRAPH 2024 Conference Papers. SIGGRAPH:
    Computer Graphics and Interactive Techniques Conference, 41.'
  mla: 'Rao, Pramod, et al. “Lite2Relight: 3D-Aware Single Image Portrait Relighting.”
    <i>Proceedings - SIGGRAPH 2024 Conference Papers</i>, 41, Association for Computing
    Machinery, 2024, doi:<a href="https://doi.org/10.1145/3641519.3657470">10.1145/3641519.3657470</a>.'
  short: P. Rao, G. Fox, A. Meka, B.R. Mallikarjun, F. Zhan, T. Weyrich, B. Bickel,
    H. Pfister, W. Matusik, M. Elgharib, C. Theobalt, in:, Proceedings - SIGGRAPH
    2024 Conference Papers, Association for Computing Machinery, 2024.
conference:
  end_date: 2024-08-01
  location: Denver, CO, United States
  name: 'SIGGRAPH: Computer Graphics and Interactive Techniques Conference'
  start_date: 2024-07-27
das_tickbox: '0'
date_created: 2024-08-04T22:01:21Z
date_published: 2024-07-13T00:00:00Z
date_updated: 2026-09-24T11:00:21Z
day: '13'
ddc:
- '000'
department:
- _id: BeBi
doi: 10.1145/3641519.3657470
external_id:
  arxiv:
  - '2407.10487'
  isi:
  - '001282218200076'
file:
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  checksum: 4650f6d1419e675929133e46a91ca177
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  creator: dernst
  date_created: 2024-08-05T08:25:18Z
  date_updated: 2024-08-05T08:25:18Z
  file_id: '17387'
  file_name: 2024_SIGGRAPH_Rao.pdf
  file_size: 59683257
  relation: main_file
  success: 1
file_date_updated: 2024-08-05T08:25:18Z
fulldoi: https://doi.org/10.1145/3641519.3657470
has_accepted_license: '1'
isi: 1
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
publication: Proceedings - SIGGRAPH 2024 Conference Papers
publication_identifier:
  isbn:
  - '9798400705250'
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: yes
title: 'Lite2Relight: 3D-aware single image portrait relighting'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
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  short: CC BY (4.0)
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
year: '2024'
...
---
APC_amount: 12348 EUR
OA_place: publisher
OA_type: hybrid
_id: '17460'
abstract:
- lang: eng
  text: Filaments in the cell commonly treadmill. Driven by energy consumption, they
    grow on one end while shrinking on the other, causing filaments to appear motile
    even though individual proteins remain static. This process is characteristic
    of cytoskeletal filaments and leads to collective filament self-organization.
    Here we show that treadmilling drives filament nematic ordering by dissolving
    misaligned filaments. Taking the bacterial FtsZ protein involved in cell division
    as an example, we show that this mechanism aligns FtsZ filaments in vitro and
    drives the organization of the division ring in living Bacillus subtilis cells.
    We find that ordering via local dissolution also allows the system to quickly
    respond to chemical and geometrical biases in the cell, enabling us to quantitatively
    explain the ring formation dynamics in vivo. Beyond FtsZ and other cytoskeletal
    filaments, our study identifies a mechanism for self-organization via constant
    birth and death of energy-consuming filaments.
acknowledgement: We thank I. Palaia (ISTA) for useful discussions and K. Lim and R.
  W. Wong (WPI-Nano Life Science Institute, Kanazawa University) for providing access
  to HS-AFM. We would like to thank B. Prats Mateu (MSD Austria, Vienna) for providing
  the HS-AFM data. This work was supported by the Royal Society (grant no. UF160266;
  C.V.-C. and A.Š.), the European Union’s Horizon 2020 Research and Innovation Programme
  (grant no. 802960; A.Š.), the Austrian Science Fund (FWF) Stand-Alone P34607 (M.L.)
  and a Wellcome Trust and Royal Society Sir Henry Dale Fellowship (grant no. 206670/Z/17/Z;
  S.H. and K.D.W.).
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Christian Eduardo
  full_name: Vanhille-Campos, Christian Eduardo
  id: 3adeca52-9313-11ed-b1ac-c170b2505714
  last_name: Vanhille-Campos
- first_name: Kevin D.
  full_name: Whitley, Kevin D.
  last_name: Whitley
- first_name: Philipp
  full_name: Radler, Philipp
  id: 40136C2A-F248-11E8-B48F-1D18A9856A87
  last_name: Radler
  orcid: '0000-0001-9198-2182 '
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
- first_name: Séamus
  full_name: Holden, Séamus
  last_name: Holden
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
citation:
  ama: Vanhille-Campos CE, Whitley KD, Radler P, Loose M, Holden S, Šarić A. Self-organization
    of mortal filaments and its role in bacterial division ring formation. <i>Nature
    Physics</i>. 2024;20:1670-1678. doi:<a href="https://doi.org/10.1038/s41567-024-02597-8">10.1038/s41567-024-02597-8</a>
  apa: Vanhille-Campos, C. E., Whitley, K. D., Radler, P., Loose, M., Holden, S.,
    &#38; Šarić, A. (2024). Self-organization of mortal filaments and its role in
    bacterial division ring formation. <i>Nature Physics</i>. Springer Nature. <a
    href="https://doi.org/10.1038/s41567-024-02597-8">https://doi.org/10.1038/s41567-024-02597-8</a>
  chicago: Vanhille-Campos, Christian Eduardo, Kevin D. Whitley, Philipp Radler, Martin
    Loose, Séamus Holden, and Anđela Šarić. “Self-Organization of Mortal Filaments
    and Its Role in Bacterial Division Ring Formation.” <i>Nature Physics</i>. Springer
    Nature, 2024. <a href="https://doi.org/10.1038/s41567-024-02597-8">https://doi.org/10.1038/s41567-024-02597-8</a>.
  ieee: C. E. Vanhille-Campos, K. D. Whitley, P. Radler, M. Loose, S. Holden, and
    A. Šarić, “Self-organization of mortal filaments and its role in bacterial division
    ring formation,” <i>Nature Physics</i>, vol. 20. Springer Nature, pp. 1670–1678,
    2024.
  ista: Vanhille-Campos CE, Whitley KD, Radler P, Loose M, Holden S, Šarić A. 2024.
    Self-organization of mortal filaments and its role in bacterial division ring
    formation. Nature Physics. 20, 1670–1678.
  mla: Vanhille-Campos, Christian Eduardo, et al. “Self-Organization of Mortal Filaments
    and Its Role in Bacterial Division Ring Formation.” <i>Nature Physics</i>, vol.
    20, Springer Nature, 2024, pp. 1670–78, doi:<a href="https://doi.org/10.1038/s41567-024-02597-8">10.1038/s41567-024-02597-8</a>.
  short: C.E. Vanhille-Campos, K.D. Whitley, P. Radler, M. Loose, S. Holden, A. Šarić,
    Nature Physics 20 (2024) 1670–1678.
corr_author: '1'
das_tickbox: '1'
dataavailabilitystatement: The simulation data presented in this work are available
  from the University College London public data repository at https://doi.org/10.5522/04/24754527
  (ref. 74). Live-cell imaging of FtsZ rings data presented in this work are from
  ref. 23. High-speed atomic force microscopy data presented in this work are from
  ref. 9. Total internal reflection fluorescence microscopy data presented in this
  work are from refs. 37,75,76
date_created: 2024-08-25T22:01:08Z
date_published: 2024-10-01T00:00:00Z
date_updated: 2026-09-24T10:58:39Z
day: '01'
ddc:
- '570'
department:
- _id: AnSa
- _id: MaLo
doi: 10.1038/s41567-024-02597-8
ec_funded: 1
external_id:
  isi:
  - '001289394500005'
  pmid:
  - '39416851'
file:
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  date_created: 2025-04-14T06:06:35Z
  date_updated: 2025-04-14T06:06:35Z
  file_id: '19556'
  file_name: 2024_NaturePhysics_VanhilleCampos.pdf
  file_size: 8058249
  relation: main_file
  success: 1
file_date_updated: 2025-04-14T06:06:35Z
fulldoi: https://doi.org/10.1038/s41567-024-02597-8
has_accepted_license: '1'
intvolume: '        20'
isi: 1
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 1670-1678
pmid: 1
popular_science: '1'
project:
- _id: fc38323b-9c52-11eb-aca3-ff8afb4a011d
  grant_number: P34607
  name: In vitro reconstitution of bacterial cell division
- _id: eba2549b-77a9-11ec-83b8-a81e493eae4e
  call_identifier: H2020
  grant_number: '802960'
  name: 'Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines'
publication: Nature Physics
publication_identifier:
  eissn:
  - 1745-2481
  issn:
  - 1745-2473
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  record:
  - id: '22988'
    relation: research_data
    status: public
researchdata_availability: yes
scopus_import: '1'
status: public
supplementarymaterial: yes
title: Self-organization of mortal filaments and its role in bacterial division ring
  formation
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: 20
year: '2024'
...
---
_id: '14488'
abstract:
- lang: eng
  text: 'Portrait viewpoint and illumination editing is an important problem with
    several applications in VR/AR, movies, and photography. Comprehensive knowledge
    of geometry and illumination is critical for obtaining photorealistic results.
    Current methods are unable to explicitly model in 3D while handling both viewpoint
    and illumination editing from a single image. In this paper, we propose VoRF,
    a novel approach that can take even a single portrait image as input and relight
    human heads under novel illuminations that can be viewed from arbitrary viewpoints.
    VoRF represents a human head as a continuous volumetric field and learns a prior
    model of human heads using a coordinate-based MLP with individual latent spaces
    for identity and illumination. The prior model is learned in an auto-decoder manner
    over a diverse class of head shapes and appearances, allowing VoRF to generalize
    to novel test identities from a single input image. Additionally, VoRF has a reflectance
    MLP that uses the intermediate features of the prior model for rendering One-Light-at-A-Time
    (OLAT) images under novel views. We synthesize novel illuminations by combining
    these OLAT images with target environment maps. Qualitative and quantitative evaluations
    demonstrate the effectiveness of VoRF for relighting and novel view synthesis,
    even when applied to unseen subjects under uncontrolled illumination. This work
    is an extension of Rao et al. (VoRF: Volumetric Relightable Faces 2022). We provide
    extensive evaluation and ablative studies of our model and also provide an application,
    where any face can be relighted using textual input.'
acknowledgement: Open Access funding enabled and organized by Projekt DEAL.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Pramod
  full_name: Rao, Pramod
  last_name: Rao
- first_name: B. R.
  full_name: Mallikarjun, B. R.
  last_name: Mallikarjun
- first_name: Gereon
  full_name: Fox, Gereon
  last_name: Fox
- first_name: Tim
  full_name: Weyrich, Tim
  last_name: Weyrich
- first_name: Bernd
  full_name: Bickel, Bernd
  id: 49876194-F248-11E8-B48F-1D18A9856A87
  last_name: Bickel
  orcid: 0000-0001-6511-9385
- first_name: Hanspeter
  full_name: Pfister, Hanspeter
  last_name: Pfister
- first_name: Wojciech
  full_name: Matusik, Wojciech
  last_name: Matusik
- first_name: Fangneng
  full_name: Zhan, Fangneng
  last_name: Zhan
- first_name: Ayush
  full_name: Tewari, Ayush
  last_name: Tewari
- first_name: Christian
  full_name: Theobalt, Christian
  last_name: Theobalt
- first_name: Mohamed
  full_name: Elgharib, Mohamed
  last_name: Elgharib
citation:
  ama: Rao P, Mallikarjun BR, Fox G, et al. A deeper analysis of volumetric relightiable
    faces. <i>International Journal of Computer Vision</i>. 2024;132:1148-1166. doi:<a
    href="https://doi.org/10.1007/s11263-023-01899-3">10.1007/s11263-023-01899-3</a>
  apa: Rao, P., Mallikarjun, B. R., Fox, G., Weyrich, T., Bickel, B., Pfister, H.,
    … Elgharib, M. (2024). A deeper analysis of volumetric relightiable faces. <i>International
    Journal of Computer Vision</i>. Springer Nature. <a href="https://doi.org/10.1007/s11263-023-01899-3">https://doi.org/10.1007/s11263-023-01899-3</a>
  chicago: Rao, Pramod, B. R. Mallikarjun, Gereon Fox, Tim Weyrich, Bernd Bickel,
    Hanspeter Pfister, Wojciech Matusik, et al. “A Deeper Analysis of Volumetric Relightiable
    Faces.” <i>International Journal of Computer Vision</i>. Springer Nature, 2024.
    <a href="https://doi.org/10.1007/s11263-023-01899-3">https://doi.org/10.1007/s11263-023-01899-3</a>.
  ieee: P. Rao <i>et al.</i>, “A deeper analysis of volumetric relightiable faces,”
    <i>International Journal of Computer Vision</i>, vol. 132. Springer Nature, pp.
    1148–1166, 2024.
  ista: Rao P, Mallikarjun BR, Fox G, Weyrich T, Bickel B, Pfister H, Matusik W, Zhan
    F, Tewari A, Theobalt C, Elgharib M. 2024. A deeper analysis of volumetric relightiable
    faces. International Journal of Computer Vision. 132, 1148–1166.
  mla: Rao, Pramod, et al. “A Deeper Analysis of Volumetric Relightiable Faces.” <i>International
    Journal of Computer Vision</i>, vol. 132, Springer Nature, 2024, pp. 1148–66,
    doi:<a href="https://doi.org/10.1007/s11263-023-01899-3">10.1007/s11263-023-01899-3</a>.
  short: P. Rao, B.R. Mallikarjun, G. Fox, T. Weyrich, B. Bickel, H. Pfister, W. Matusik,
    F. Zhan, A. Tewari, C. Theobalt, M. Elgharib, International Journal of Computer
    Vision 132 (2024) 1148–1166.
das_tickbox: '1'
dataavailabilitystatement: 'Due to privacy concerns, we cannot make the dataset used
  in our project publicly available. However, to demonstrate the effectiveness of
  our proposed method, we evaluate our approach using publicly available datasets
  such as H3DS (Ramon et al., 2021): https://github.com/CrisalixSA/h3ds, FFHQ (Karras
  et al., 2021): https://github.com/NVlabs/ffhq-dataset, and CelebA (Liu et al., 2015):
  https://mmlab.ie.cuhk.edu.hk/projects/CelebA.html. Using these datasets allows us
  to evaluate the generalization ability of our proposed method on unseen data. H3DS
  provides high-quality 3D scans of human faces, FFHQ contains high-resolution facial
  images, and CelebA is a large-scale dataset of celebrity faces. We use these datasets
  to evaluate the performance of our proposed method in various scenarios, such as
  face rotation and relighting, and compare them with state-of-the-art methods.'
date_created: 2023-11-05T23:00:54Z
date_published: 2024-04-01T00:00:00Z
date_updated: 2026-09-24T10:59:50Z
day: '01'
ddc:
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department:
- _id: BeBi
doi: 10.1007/s11263-023-01899-3
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fulldoi: https://doi.org/10.1007/s11263-023-01899-3
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isi: 1
language:
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month: '04'
oa: 1
oa_version: Published Version
page: 1148-1166
pmid: 1
publication: International Journal of Computer Vision
publication_identifier:
  eissn:
  - 1573-1405
  issn:
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publication_status: published
publisher: Springer Nature
quality_controlled: '1'
researchdata_availability: no (restricted access)
scopus_import: '1'
status: public
supplementarymaterial: no
title: A deeper analysis of volumetric relightiable faces
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  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
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  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 132
year: '2024'
...
