---
_id: '9060'
abstract:
- lang: eng
text: Molecular motors are essential to the living, generating fluctuations that
boost transport and assist assembly. Active colloids, that consume energy to move,
hold similar potential for man-made materials controlled by forces generated from
within. Yet, their use as a powerhouse in materials science lacks. Here we show
a massive acceleration of the annealing of a monolayer of passive beads by moderate
addition of self-propelled microparticles. We rationalize our observations with
a model of collisions that drive active fluctuations and activate the annealing.
The experiment is quantitatively compared with Brownian dynamic simulations that
further unveil a dynamical transition in the mechanism of annealing. Active dopants
travel uniformly in the system or co-localize at the grain boundaries as a result
of the persistence of their motion. Our findings uncover the potential of internal
activity to control materials and lay the groundwork for the rise of materials
science beyond equilibrium.
article_number: '3380'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Sophie
full_name: Ramananarivo, Sophie
last_name: Ramananarivo
- first_name: Etienne
full_name: Ducrot, Etienne
last_name: Ducrot
- first_name: Jérémie A
full_name: Palacci, Jérémie A
id: 8fb92548-2b22-11eb-b7c1-a3f0d08d7c7d
last_name: Palacci
orcid: 0000-0002-7253-9465
citation:
ama: Ramananarivo S, Ducrot E, Palacci JA. Activity-controlled annealing of colloidal
monolayers. Nature Communications. 2019;10(1). doi:10.1038/s41467-019-11362-y
apa: Ramananarivo, S., Ducrot, E., & Palacci, J. A. (2019). Activity-controlled
annealing of colloidal monolayers. Nature Communications. Springer Nature.
https://doi.org/10.1038/s41467-019-11362-y
chicago: Ramananarivo, Sophie, Etienne Ducrot, and Jérémie A Palacci. “Activity-Controlled
Annealing of Colloidal Monolayers.” Nature Communications. Springer Nature,
2019. https://doi.org/10.1038/s41467-019-11362-y.
ieee: S. Ramananarivo, E. Ducrot, and J. A. Palacci, “Activity-controlled annealing
of colloidal monolayers,” Nature Communications, vol. 10, no. 1. Springer
Nature, 2019.
ista: Ramananarivo S, Ducrot E, Palacci JA. 2019. Activity-controlled annealing
of colloidal monolayers. Nature Communications. 10(1), 3380.
mla: Ramananarivo, Sophie, et al. “Activity-Controlled Annealing of Colloidal Monolayers.”
Nature Communications, vol. 10, no. 1, 3380, Springer Nature, 2019, doi:10.1038/s41467-019-11362-y.
short: S. Ramananarivo, E. Ducrot, J.A. Palacci, Nature Communications 10 (2019).
date_created: 2021-02-02T13:43:36Z
date_published: 2019-07-29T00:00:00Z
date_updated: 2023-02-23T13:47:59Z
day: '29'
ddc:
- '530'
doi: 10.1038/s41467-019-11362-y
extern: '1'
external_id:
arxiv:
- '1909.07382'
pmid:
- '31358762'
file:
- access_level: open_access
checksum: 70c6e5d6fbea0932b0669505ab6633ec
content_type: application/pdf
creator: cziletti
date_created: 2021-02-02T13:47:21Z
date_updated: 2021-02-02T13:47:21Z
file_id: '9061'
file_name: 2019_NatureComm_Ramananarivo.pdf
file_size: 2820337
relation: main_file
success: 1
file_date_updated: 2021-02-02T13:47:21Z
has_accepted_license: '1'
intvolume: ' 10'
issue: '1'
keyword:
- General Biochemistry
- Genetics and Molecular Biology
- General Physics and Astronomy
- General Chemistry
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Activity-controlled annealing of colloidal monolayers
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: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 10
year: '2019'
...
---
_id: '13374'
abstract:
- lang: eng
text: Confining molecules to volumes only slightly larger than the molecules themselves
can profoundly alter their properties. Molecular switches—entities that can be
toggled between two or more forms upon exposure to an external stimulus—often
require conformational freedom to isomerize. Therefore, placing these switches
in confined spaces can render them non-operational. To preserve the switchability
of these species under confinement, we work with a water-soluble coordination
cage that is flexible enough to adapt its shape to the conformation of the encapsulated
guest. We show that owing to its flexibility, the cage is not only capable of
accommodating—and solubilizing in water—several light-responsive spiropyran-based
molecular switches, but, more importantly, it also provides an environment suitable
for the efficient, reversible photoisomerization of the bound guests. Our findings
pave the way towards studying various molecular switching processes in confined
environments.
article_number: '641'
article_processing_charge: No
article_type: original
author:
- first_name: Dipak
full_name: Samanta, Dipak
last_name: Samanta
- first_name: Daria
full_name: Galaktionova, Daria
last_name: Galaktionova
- first_name: Julius
full_name: Gemen, Julius
last_name: Gemen
- first_name: Linda J. W.
full_name: Shimon, Linda J. W.
last_name: Shimon
- first_name: Yael
full_name: Diskin-Posner, Yael
last_name: Diskin-Posner
- first_name: Liat
full_name: Avram, Liat
last_name: Avram
- first_name: Petr
full_name: Král, Petr
last_name: Král
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: Samanta D, Galaktionova D, Gemen J, et al. Reversible chromism of spiropyran
in the cavity of a flexible coordination cage. Nature Communications. 2018;9.
doi:10.1038/s41467-017-02715-6
apa: Samanta, D., Galaktionova, D., Gemen, J., Shimon, L. J. W., Diskin-Posner,
Y., Avram, L., … Klajn, R. (2018). Reversible chromism of spiropyran in the cavity
of a flexible coordination cage. Nature Communications. Springer Nature.
https://doi.org/10.1038/s41467-017-02715-6
chicago: Samanta, Dipak, Daria Galaktionova, Julius Gemen, Linda J. W. Shimon, Yael
Diskin-Posner, Liat Avram, Petr Král, and Rafal Klajn. “Reversible Chromism of
Spiropyran in the Cavity of a Flexible Coordination Cage.” Nature Communications.
Springer Nature, 2018. https://doi.org/10.1038/s41467-017-02715-6.
ieee: D. Samanta et al., “Reversible chromism of spiropyran in the cavity
of a flexible coordination cage,” Nature Communications, vol. 9. Springer
Nature, 2018.
ista: Samanta D, Galaktionova D, Gemen J, Shimon LJW, Diskin-Posner Y, Avram L,
Král P, Klajn R. 2018. Reversible chromism of spiropyran in the cavity of a flexible
coordination cage. Nature Communications. 9, 641.
mla: Samanta, Dipak, et al. “Reversible Chromism of Spiropyran in the Cavity of
a Flexible Coordination Cage.” Nature Communications, vol. 9, 641, Springer
Nature, 2018, doi:10.1038/s41467-017-02715-6.
short: D. Samanta, D. Galaktionova, J. Gemen, L.J.W. Shimon, Y. Diskin-Posner, L.
Avram, P. Král, R. Klajn, Nature Communications 9 (2018).
date_created: 2023-08-01T09:39:32Z
date_published: 2018-02-13T00:00:00Z
date_updated: 2024-10-14T12:14:34Z
day: '13'
doi: 10.1038/s41467-017-02715-6
extern: '1'
external_id:
pmid:
- '29440687'
intvolume: ' 9'
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1038/s41467-017-02715-6
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
eissn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
link:
- relation: erratum
url: https://doi.org/10.1038/s41467-018-03701-2
scopus_import: '1'
status: public
title: Reversible chromism of spiropyran in the cavity of a flexible coordination
cage
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 9
year: '2018'
...
---
_id: '14003'
abstract:
- lang: eng
text: "Molecular chirality plays an essential role in most biochemical processes.
The observation and quantification of chirality-sensitive signals, however, remains
extremely challenging, especially on ultrafast timescales and in dilute media.
Here, we describe the experimental realization of an all-optical and ultrafast
scheme for detecting chiral dynamics in molecules. This technique is based on
high-harmonic generation by a combination of two-color counterrotating femtosecond
laser pulses with polarization states tunable from linear to circular. We demonstrate
two different implementations of chiral-sensitive high-harmonic spectroscopy on
an ensemble of randomly oriented methyloxirane molecules in the gas phase. Using
two elliptically polarized fields, we observe that the ellipticities maximizing
the harmonic signal reach up to \r\n4.4\r\n±\r\n0.2\r\n%\r\n (at 17.6 eV). Using
two circularly polarized fields, we observe circular dichroisms ranging up to
\r\n13\r\n±\r\n6\r\n%\r\n (28.3–33.1 eV). Our theoretical analysis confirms that
the observed chiral response originates from subfemtosecond electron dynamics
driven by the magnetic component of the driving laser field. This assignment is
supported by the experimental observation of a strong intensity dependence of
the chiral effects and its agreement with theory. We moreover report and explain
a pronounced variation of the signal strength and dichroism with the driving-field
ellipticities and harmonic orders. Finally, we demonstrate the sensitivity of
the experimental observables to the shape of the electron hole. This technique
for chiral discrimination will yield femtosecond temporal resolution when integrated
in a pump-probe scheme and subfemtosecond resolution on chiral charge migration
in a self-probing scheme."
article_number: '031060'
article_processing_charge: No
article_type: original
author:
- first_name: Denitsa Rangelova
full_name: Baykusheva, Denitsa Rangelova
id: 71b4d059-2a03-11ee-914d-dfa3beed6530
last_name: Baykusheva
- first_name: Hans Jakob
full_name: Wörner, Hans Jakob
last_name: Wörner
citation:
ama: Baykusheva DR, Wörner HJ. Chiral discrimination through bielliptical high-harmonic
spectroscopy. Physical Review X. 2018;8(3). doi:10.1103/physrevx.8.031060
apa: Baykusheva, D. R., & Wörner, H. J. (2018). Chiral discrimination through
bielliptical high-harmonic spectroscopy. Physical Review X. American Physical
Society. https://doi.org/10.1103/physrevx.8.031060
chicago: Baykusheva, Denitsa Rangelova, and Hans Jakob Wörner. “Chiral Discrimination
through Bielliptical High-Harmonic Spectroscopy.” Physical Review X. American
Physical Society, 2018. https://doi.org/10.1103/physrevx.8.031060.
ieee: D. R. Baykusheva and H. J. Wörner, “Chiral discrimination through bielliptical
high-harmonic spectroscopy,” Physical Review X, vol. 8, no. 3. American
Physical Society, 2018.
ista: Baykusheva DR, Wörner HJ. 2018. Chiral discrimination through bielliptical
high-harmonic spectroscopy. Physical Review X. 8(3), 031060.
mla: Baykusheva, Denitsa Rangelova, and Hans Jakob Wörner. “Chiral Discrimination
through Bielliptical High-Harmonic Spectroscopy.” Physical Review X, vol.
8, no. 3, 031060, American Physical Society, 2018, doi:10.1103/physrevx.8.031060.
short: D.R. Baykusheva, H.J. Wörner, Physical Review X 8 (2018).
date_created: 2023-08-10T06:34:48Z
date_published: 2018-07-01T00:00:00Z
date_updated: 2023-08-22T07:42:07Z
day: '01'
doi: 10.1103/physrevx.8.031060
extern: '1'
intvolume: ' 8'
issue: '3'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1103/PhysRevX.8.031060
month: '07'
oa: 1
oa_version: Published Version
publication: Physical Review X
publication_identifier:
eissn:
- 2160-3308
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Chiral discrimination through bielliptical high-harmonic spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2018'
...
---
_id: '14284'
abstract:
- lang: eng
text: Pore-forming toxins (PFT) are virulence factors that transform from soluble
to membrane-bound states. The Yersinia YaxAB system represents a family of binary
α-PFTs with orthologues in human, insect, and plant pathogens, with unknown structures.
YaxAB was shown to be cytotoxic and likely involved in pathogenesis, though the
molecular basis for its two-component lytic mechanism remains elusive. Here, we
present crystal structures of YaxA and YaxB, together with a cryo-electron microscopy
map of the YaxAB complex. Our structures reveal a pore predominantly composed
of decamers of YaxA–YaxB heterodimers. Both subunits bear membrane-active moieties,
but only YaxA is capable of binding to membranes by itself. YaxB can subsequently
be recruited to membrane-associated YaxA and induced to present its lytic transmembrane
helices. Pore formation can progress by further oligomerization of YaxA–YaxB dimers.
Our results allow for a comparison between pore assemblies belonging to the wider
ClyA-like family of α-PFTs, highlighting diverse pore architectures.
article_number: '1806'
article_processing_charge: No
article_type: original
author:
- first_name: Bastian
full_name: Bräuning, Bastian
last_name: Bräuning
- first_name: Eva
full_name: Bertosin, Eva
last_name: Bertosin
- first_name: Florian M
full_name: Praetorius, Florian M
id: dfec9381-4341-11ee-8fd8-faa02bba7d62
last_name: Praetorius
- first_name: Christian
full_name: Ihling, Christian
last_name: Ihling
- first_name: Alexandra
full_name: Schatt, Alexandra
last_name: Schatt
- first_name: Agnes
full_name: Adler, Agnes
last_name: Adler
- first_name: Klaus
full_name: Richter, Klaus
last_name: Richter
- first_name: Andrea
full_name: Sinz, Andrea
last_name: Sinz
- first_name: Hendrik
full_name: Dietz, Hendrik
last_name: Dietz
- first_name: Michael
full_name: Groll, Michael
last_name: Groll
citation:
ama: Bräuning B, Bertosin E, Praetorius FM, et al. Structure and mechanism of the
two-component α-helical pore-forming toxin YaxAB. Nature Communications.
2018;9. doi:10.1038/s41467-018-04139-2
apa: Bräuning, B., Bertosin, E., Praetorius, F. M., Ihling, C., Schatt, A., Adler,
A., … Groll, M. (2018). Structure and mechanism of the two-component α-helical
pore-forming toxin YaxAB. Nature Communications. Springer Nature. https://doi.org/10.1038/s41467-018-04139-2
chicago: Bräuning, Bastian, Eva Bertosin, Florian M Praetorius, Christian Ihling,
Alexandra Schatt, Agnes Adler, Klaus Richter, Andrea Sinz, Hendrik Dietz, and
Michael Groll. “Structure and Mechanism of the Two-Component α-Helical Pore-Forming
Toxin YaxAB.” Nature Communications. Springer Nature, 2018. https://doi.org/10.1038/s41467-018-04139-2.
ieee: B. Bräuning et al., “Structure and mechanism of the two-component α-helical
pore-forming toxin YaxAB,” Nature Communications, vol. 9. Springer Nature,
2018.
ista: Bräuning B, Bertosin E, Praetorius FM, Ihling C, Schatt A, Adler A, Richter
K, Sinz A, Dietz H, Groll M. 2018. Structure and mechanism of the two-component
α-helical pore-forming toxin YaxAB. Nature Communications. 9, 1806.
mla: Bräuning, Bastian, et al. “Structure and Mechanism of the Two-Component α-Helical
Pore-Forming Toxin YaxAB.” Nature Communications, vol. 9, 1806, Springer
Nature, 2018, doi:10.1038/s41467-018-04139-2.
short: B. Bräuning, E. Bertosin, F.M. Praetorius, C. Ihling, A. Schatt, A. Adler,
K. Richter, A. Sinz, H. Dietz, M. Groll, Nature Communications 9 (2018).
date_created: 2023-09-06T12:07:33Z
date_published: 2018-05-04T00:00:00Z
date_updated: 2023-11-07T11:46:12Z
day: '04'
doi: 10.1038/s41467-018-04139-2
extern: '1'
external_id:
pmid:
- '29728606'
intvolume: ' 9'
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1038/s41467-018-04139-2
month: '05'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Structure and mechanism of the two-component α-helical pore-forming toxin YaxAB
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 9
year: '2018'
...
---
_id: '15232'
abstract:
- lang: eng
text: 'In this paper we describe the potential of the enhanced X-ray Timing and
Polarimetry (eXTP) mission for studies related to accretion flows in the strong
field gravity regime around both stellar-mass and supermassive black-holes. eXTP
has the unique capability of using advanced “spectral-timing-polarimetry” techniques
to analyze the rapid variations with three orthogonal diagnostics of the flow
and its geometry, yielding unprecedented insight into the inner accreting regions,
the effects of strong field gravity on the material within them and the powerful
outflows which are driven by the accretion process. '
article_number: '29504'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Alessandra De
full_name: Rosa, Alessandra De
last_name: Rosa
- first_name: Phil
full_name: Uttley, Phil
last_name: Uttley
- first_name: LiJun
full_name: Gou, LiJun
last_name: Gou
- first_name: Yuan
full_name: Liu, Yuan
last_name: Liu
- first_name: Cosimo
full_name: Bambi, Cosimo
last_name: Bambi
- first_name: Didier
full_name: Barret, Didier
last_name: Barret
- first_name: Tomaso
full_name: Belloni, Tomaso
last_name: Belloni
- first_name: Emanuele
full_name: Berti, Emanuele
last_name: Berti
- first_name: Stefano
full_name: Bianchi, Stefano
last_name: Bianchi
- first_name: Ilaria
full_name: Caiazzo, Ilaria
id: 8ae5b6e7-2a03-11ee-914d-b58ed7a3b47d
last_name: Caiazzo
orcid: 0000-0002-4770-5388
- first_name: Piergiorgio
full_name: Casella, Piergiorgio
last_name: Casella
- first_name: Marco
full_name: Feroci, Marco
last_name: Feroci
- first_name: Valeria
full_name: Ferrari, Valeria
last_name: Ferrari
- first_name: Leonardo
full_name: Gualtieri, Leonardo
last_name: Gualtieri
- first_name: Jeremy
full_name: Heyl, Jeremy
last_name: Heyl
- first_name: Adam
full_name: Ingram, Adam
last_name: Ingram
- first_name: Vladimir
full_name: Karas, Vladimir
last_name: Karas
- first_name: FangJun
full_name: Lu, FangJun
last_name: Lu
- first_name: Bin
full_name: Luo, Bin
last_name: Luo
- first_name: Giorgio
full_name: Matt, Giorgio
last_name: Matt
- first_name: Sara
full_name: Motta, Sara
last_name: Motta
- first_name: Joseph
full_name: Neilsen, Joseph
last_name: Neilsen
- first_name: Paolo
full_name: Pani, Paolo
last_name: Pani
- first_name: Andrea
full_name: Santangelo, Andrea
last_name: Santangelo
- first_name: XinWen
full_name: Shu, XinWen
last_name: Shu
- first_name: JunFeng
full_name: Wang, JunFeng
last_name: Wang
- first_name: Jian-Min
full_name: Wang, Jian-Min
last_name: Wang
- first_name: YongQuan
full_name: Xue, YongQuan
last_name: Xue
- first_name: YuPeng
full_name: Xu, YuPeng
last_name: Xu
- first_name: WeiMin
full_name: Yuan, WeiMin
last_name: Yuan
- first_name: YeFei
full_name: Yuan, YeFei
last_name: Yuan
- first_name: Shuang-Nan
full_name: Zhang, Shuang-Nan
last_name: Zhang
- first_name: Shu
full_name: Zhang, Shu
last_name: Zhang
- first_name: Ivan
full_name: Agudo, Ivan
last_name: Agudo
- first_name: Lorenzo
full_name: Amati, Lorenzo
last_name: Amati
- first_name: Nils
full_name: Andersson, Nils
last_name: Andersson
- first_name: Cristina
full_name: Baglio, Cristina
last_name: Baglio
- first_name: Pavel
full_name: Bakala, Pavel
last_name: Bakala
- first_name: Altan
full_name: Baykal, Altan
last_name: Baykal
- first_name: Sudip
full_name: Bhattacharyya, Sudip
last_name: Bhattacharyya
- first_name: Ignazio
full_name: Bombaci, Ignazio
last_name: Bombaci
- first_name: Niccoló
full_name: Bucciantini, Niccoló
last_name: Bucciantini
- first_name: Fiamma
full_name: Capitanio, Fiamma
last_name: Capitanio
- first_name: Riccardo
full_name: Ciolfi, Riccardo
last_name: Ciolfi
- first_name: Wei K.
full_name: Cui, Wei K.
last_name: Cui
- first_name: Filippo
full_name: D’Ammando, Filippo
last_name: D’Ammando
- first_name: Thomas
full_name: Dauser, Thomas
last_name: Dauser
- first_name: Melania
full_name: Del Santo, Melania
last_name: Del Santo
- first_name: Barbara
full_name: De Marco, Barbara
last_name: De Marco
- first_name: Tiziana
full_name: Di Salvo, Tiziana
last_name: Di Salvo
- first_name: Chris
full_name: Done, Chris
last_name: Done
- first_name: Michal
full_name: Dovčiak, Michal
last_name: Dovčiak
- first_name: Andrew C.
full_name: Fabian, Andrew C.
last_name: Fabian
- first_name: Maurizio
full_name: Falanga, Maurizio
last_name: Falanga
- first_name: Angelo Francesco
full_name: Gambino, Angelo Francesco
last_name: Gambino
- first_name: Bruce
full_name: Gendre, Bruce
last_name: Gendre
- first_name: Victoria
full_name: Grinberg, Victoria
last_name: Grinberg
- first_name: Alexander
full_name: Heger, Alexander
last_name: Heger
- first_name: Jeroen
full_name: Homan, Jeroen
last_name: Homan
- first_name: Rosario
full_name: Iaria, Rosario
last_name: Iaria
- first_name: JiaChen
full_name: Jiang, JiaChen
last_name: Jiang
- first_name: ChiChuan
full_name: Jin, ChiChuan
last_name: Jin
- first_name: Elmar
full_name: Koerding, Elmar
last_name: Koerding
- first_name: Manu
full_name: Linares, Manu
last_name: Linares
- first_name: Zhu
full_name: Liu, Zhu
last_name: Liu
- first_name: Thomas J.
full_name: Maccarone, Thomas J.
last_name: Maccarone
- first_name: Julien
full_name: Malzac, Julien
last_name: Malzac
- first_name: Antonios
full_name: Manousakis, Antonios
last_name: Manousakis
- first_name: Frédéric
full_name: Marin, Frédéric
last_name: Marin
- first_name: Andrea
full_name: Marinucci, Andrea
last_name: Marinucci
- first_name: Missagh
full_name: Mehdipour, Missagh
last_name: Mehdipour
- first_name: Mariano
full_name: Méndez, Mariano
last_name: Méndez
- first_name: Simone
full_name: Migliari, Simone
last_name: Migliari
- first_name: Cole
full_name: Miller, Cole
last_name: Miller
- first_name: Giovanni
full_name: Miniutti, Giovanni
last_name: Miniutti
- first_name: Emanuele
full_name: Nardini, Emanuele
last_name: Nardini
- first_name: Paul T.
full_name: O’Brien, Paul T.
last_name: O’Brien
- first_name: Julian P.
full_name: Osborne, Julian P.
last_name: Osborne
- first_name: Pierre Olivier
full_name: Petrucci, Pierre Olivier
last_name: Petrucci
- first_name: Andrea
full_name: Possenti, Andrea
last_name: Possenti
- first_name: Alessandro
full_name: Riggio, Alessandro
last_name: Riggio
- first_name: Jerome
full_name: Rodriguez, Jerome
last_name: Rodriguez
- first_name: Andrea
full_name: Sanna, Andrea
last_name: Sanna
- first_name: LiJing
full_name: Shao, LiJing
last_name: Shao
- first_name: Malgosia
full_name: Sobolewska, Malgosia
last_name: Sobolewska
- first_name: Eva
full_name: Sramkova, Eva
last_name: Sramkova
- first_name: Abigail L.
full_name: Stevens, Abigail L.
last_name: Stevens
- first_name: Holger
full_name: Stiele, Holger
last_name: Stiele
- first_name: Giulia
full_name: Stratta, Giulia
last_name: Stratta
- first_name: Zdenek
full_name: Stuchlik, Zdenek
last_name: Stuchlik
- first_name: Jiri
full_name: Svoboda, Jiri
last_name: Svoboda
- first_name: Fabrizio
full_name: Tamburini, Fabrizio
last_name: Tamburini
- first_name: Thomas M.
full_name: Tauris, Thomas M.
last_name: Tauris
- first_name: Francesco
full_name: Tombesi, Francesco
last_name: Tombesi
- first_name: Gabriel
full_name: Torok, Gabriel
last_name: Torok
- first_name: Martin
full_name: Urbanec, Martin
last_name: Urbanec
- first_name: Frederic
full_name: Vincent, Frederic
last_name: Vincent
- first_name: QingWen
full_name: Wu, QingWen
last_name: Wu
- first_name: Feng
full_name: Yuan, Feng
last_name: Yuan
- first_name: Jean J. M.
full_name: in’ t Zand, Jean J. M.
last_name: in’ t Zand
- first_name: Andrzej A.
full_name: Zdziarski, Andrzej A.
last_name: Zdziarski
- first_name: XinLin
full_name: Zhou, XinLin
last_name: Zhou
citation:
ama: Rosa AD, Uttley P, Gou L, et al. Accretion in strong field gravity with eXTP.
Science China Physics, Mechanics & Astronomy. 2018;62(2). doi:10.1007/s11433-018-9297-0
apa: Rosa, A. D., Uttley, P., Gou, L., Liu, Y., Bambi, C., Barret, D., … Zhou, X.
(2018). Accretion in strong field gravity with eXTP. Science China Physics,
Mechanics & Astronomy. Springer Nature. https://doi.org/10.1007/s11433-018-9297-0
chicago: Rosa, Alessandra De, Phil Uttley, LiJun Gou, Yuan Liu, Cosimo Bambi, Didier
Barret, Tomaso Belloni, et al. “Accretion in Strong Field Gravity with EXTP.”
Science China Physics, Mechanics & Astronomy. Springer Nature, 2018.
https://doi.org/10.1007/s11433-018-9297-0.
ieee: A. D. Rosa et al., “Accretion in strong field gravity with eXTP,” Science
China Physics, Mechanics & Astronomy, vol. 62, no. 2. Springer Nature,
2018.
ista: Rosa AD et al. 2018. Accretion in strong field gravity with eXTP. Science
China Physics, Mechanics & Astronomy. 62(2), 29504.
mla: Rosa, Alessandra De, et al. “Accretion in Strong Field Gravity with EXTP.”
Science China Physics, Mechanics & Astronomy, vol. 62, no. 2, 29504,
Springer Nature, 2018, doi:10.1007/s11433-018-9297-0.
short: A.D. Rosa, P. Uttley, L. Gou, Y. Liu, C. Bambi, D. Barret, T. Belloni, E.
Berti, S. Bianchi, I. Caiazzo, P. Casella, M. Feroci, V. Ferrari, L. Gualtieri,
J. Heyl, A. Ingram, V. Karas, F. Lu, B. Luo, G. Matt, S. Motta, J. Neilsen, P.
Pani, A. Santangelo, X. Shu, J. Wang, J.-M. Wang, Y. Xue, Y. Xu, W. Yuan, Y. Yuan,
S.-N. Zhang, S. Zhang, I. Agudo, L. Amati, N. Andersson, C. Baglio, P. Bakala,
A. Baykal, S. Bhattacharyya, I. Bombaci, N. Bucciantini, F. Capitanio, R. Ciolfi,
W.K. Cui, F. D’Ammando, T. Dauser, M. Del Santo, B. De Marco, T. Di Salvo, C.
Done, M. Dovčiak, A.C. Fabian, M. Falanga, A.F. Gambino, B. Gendre, V. Grinberg,
A. Heger, J. Homan, R. Iaria, J. Jiang, C. Jin, E. Koerding, M. Linares, Z. Liu,
T.J. Maccarone, J. Malzac, A. Manousakis, F. Marin, A. Marinucci, M. Mehdipour,
M. Méndez, S. Migliari, C. Miller, G. Miniutti, E. Nardini, P.T. O’Brien, J.P.
Osborne, P.O. Petrucci, A. Possenti, A. Riggio, J. Rodriguez, A. Sanna, L. Shao,
M. Sobolewska, E. Sramkova, A.L. Stevens, H. Stiele, G. Stratta, Z. Stuchlik,
J. Svoboda, F. Tamburini, T.M. Tauris, F. Tombesi, G. Torok, M. Urbanec, F. Vincent,
Q. Wu, F. Yuan, J.J.M. in’ t Zand, A.A. Zdziarski, X. Zhou, Science China Physics,
Mechanics & Astronomy 62 (2018).
date_created: 2024-03-26T10:37:41Z
date_published: 2018-12-07T00:00:00Z
date_updated: 2024-04-05T07:12:09Z
day: '07'
doi: 10.1007/s11433-018-9297-0
extern: '1'
external_id:
arxiv:
- '1812.04022'
intvolume: ' 62'
issue: '2'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.48550/arXiv.1812.04022
month: '12'
oa: 1
oa_version: Preprint
publication: Science China Physics, Mechanics & Astronomy
publication_identifier:
eissn:
- 1869-1927
issn:
- 1674-7348
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Accretion in strong field gravity with eXTP
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 62
year: '2018'
...
---
_id: '15233'
abstract:
- lang: eng
text: In this paper we present the science potential of the enhanced X-ray Timing
and Polarimetry (eXTP) mission for studies of strongly magnetized objects. We
will focus on the physics and astrophysics of strongly magnetized objects, namely
magnetars, accreting X-ray pulsars, and rotation powered pulsars. We also discuss
the science potential of eXTP for QED studies. Developed by an international Consortium
led by the Institute of High Energy Physics of the Chinese Academy of Sciences,
the eXTP mission is expected to be launched in the mid 2020s.
article_number: '29505'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Andrea
full_name: Santangelo, Andrea
last_name: Santangelo
- first_name: Silvia
full_name: Zane, Silvia
last_name: Zane
- first_name: Hua
full_name: Feng, Hua
last_name: Feng
- first_name: RenXin
full_name: Xu, RenXin
last_name: Xu
- first_name: Victor
full_name: Doroshenko, Victor
last_name: Doroshenko
- first_name: Enrico
full_name: Bozzo, Enrico
last_name: Bozzo
- first_name: Ilaria
full_name: Caiazzo, Ilaria
id: 8ae5b6e7-2a03-11ee-914d-b58ed7a3b47d
last_name: Caiazzo
orcid: 0000-0002-4770-5388
- first_name: Francesco Coti
full_name: Zelati, Francesco Coti
last_name: Zelati
- first_name: Paolo
full_name: Esposito, Paolo
last_name: Esposito
- first_name: Denis
full_name: González-Caniulef, Denis
last_name: González-Caniulef
- first_name: Jeremy
full_name: Heyl, Jeremy
last_name: Heyl
- first_name: Daniela
full_name: Huppenkothen, Daniela
last_name: Huppenkothen
- first_name: Gianluca
full_name: Israel, Gianluca
last_name: Israel
- first_name: ZhaoSheng
full_name: Li, ZhaoSheng
last_name: Li
- first_name: Lin
full_name: Lin, Lin
last_name: Lin
- first_name: Roberto
full_name: Mignani, Roberto
last_name: Mignani
- first_name: Nanda
full_name: Rea, Nanda
last_name: Rea
- first_name: Mauro
full_name: Orlandini, Mauro
last_name: Orlandini
- first_name: Roberto
full_name: Taverna, Roberto
last_name: Taverna
- first_name: Hao
full_name: Tong, Hao
last_name: Tong
- first_name: Roberto
full_name: Turolla, Roberto
last_name: Turolla
- first_name: Cristina
full_name: Baglio, Cristina
last_name: Baglio
- first_name: Federico
full_name: Bernardini, Federico
last_name: Bernardini
- first_name: Niccolo’
full_name: Bucciantini, Niccolo’
last_name: Bucciantini
- first_name: Marco
full_name: Feroci, Marco
last_name: Feroci
- first_name: Felix
full_name: Fürst, Felix
last_name: Fürst
- first_name: Ersin
full_name: Göğüş, Ersin
last_name: Göğüş
- first_name: Can
full_name: Güngör, Can
last_name: Güngör
- first_name: Long
full_name: Ji, Long
last_name: Ji
- first_name: FangJun
full_name: Lu, FangJun
last_name: Lu
- first_name: Antonios
full_name: Manousakis, Antonios
last_name: Manousakis
- first_name: Sandro
full_name: Mereghetti, Sandro
last_name: Mereghetti
- first_name: Romana
full_name: Mikusincova, Romana
last_name: Mikusincova
- first_name: Biswajit
full_name: Paul, Biswajit
last_name: Paul
- first_name: Chanda
full_name: Prescod-Weinstein, Chanda
last_name: Prescod-Weinstein
- first_name: George
full_name: Younes, George
last_name: Younes
- first_name: Andrea
full_name: Tiengo, Andrea
last_name: Tiengo
- first_name: YuPeng
full_name: Xu, YuPeng
last_name: Xu
- first_name: Anna
full_name: Watts, Anna
last_name: Watts
- first_name: Shu
full_name: Zhang, Shu
last_name: Zhang
- first_name: Shuang-Nan
full_name: Zhan, Shuang-Nan
last_name: Zhan
citation:
ama: Santangelo A, Zane S, Feng H, et al. Physics and astrophysics of strong magnetic
field systems with eXTP. Science China Physics, Mechanics & Astronomy.
2018;62(2). doi:10.1007/s11433-018-9234-3
apa: Santangelo, A., Zane, S., Feng, H., Xu, R., Doroshenko, V., Bozzo, E., … Zhan,
S.-N. (2018). Physics and astrophysics of strong magnetic field systems with eXTP.
Science China Physics, Mechanics & Astronomy. Springer Nature. https://doi.org/10.1007/s11433-018-9234-3
chicago: Santangelo, Andrea, Silvia Zane, Hua Feng, RenXin Xu, Victor Doroshenko,
Enrico Bozzo, Ilaria Caiazzo, et al. “Physics and Astrophysics of Strong Magnetic
Field Systems with EXTP.” Science China Physics, Mechanics & Astronomy.
Springer Nature, 2018. https://doi.org/10.1007/s11433-018-9234-3.
ieee: A. Santangelo et al., “Physics and astrophysics of strong magnetic
field systems with eXTP,” Science China Physics, Mechanics & Astronomy,
vol. 62, no. 2. Springer Nature, 2018.
ista: Santangelo A, Zane S, Feng H, Xu R, Doroshenko V, Bozzo E, Caiazzo I, Zelati
FC, Esposito P, González-Caniulef D, Heyl J, Huppenkothen D, Israel G, Li Z, Lin
L, Mignani R, Rea N, Orlandini M, Taverna R, Tong H, Turolla R, Baglio C, Bernardini
F, Bucciantini N, Feroci M, Fürst F, Göğüş E, Güngör C, Ji L, Lu F, Manousakis
A, Mereghetti S, Mikusincova R, Paul B, Prescod-Weinstein C, Younes G, Tiengo
A, Xu Y, Watts A, Zhang S, Zhan S-N. 2018. Physics and astrophysics of strong
magnetic field systems with eXTP. Science China Physics, Mechanics & Astronomy.
62(2), 29505.
mla: Santangelo, Andrea, et al. “Physics and Astrophysics of Strong Magnetic Field
Systems with EXTP.” Science China Physics, Mechanics & Astronomy, vol.
62, no. 2, 29505, Springer Nature, 2018, doi:10.1007/s11433-018-9234-3.
short: A. Santangelo, S. Zane, H. Feng, R. Xu, V. Doroshenko, E. Bozzo, I. Caiazzo,
F.C. Zelati, P. Esposito, D. González-Caniulef, J. Heyl, D. Huppenkothen, G. Israel,
Z. Li, L. Lin, R. Mignani, N. Rea, M. Orlandini, R. Taverna, H. Tong, R. Turolla,
C. Baglio, F. Bernardini, N. Bucciantini, M. Feroci, F. Fürst, E. Göğüş, C. Güngör,
L. Ji, F. Lu, A. Manousakis, S. Mereghetti, R. Mikusincova, B. Paul, C. Prescod-Weinstein,
G. Younes, A. Tiengo, Y. Xu, A. Watts, S. Zhang, S.-N. Zhan, Science China Physics,
Mechanics & Astronomy 62 (2018).
date_created: 2024-03-26T10:38:05Z
date_published: 2018-10-08T00:00:00Z
date_updated: 2024-04-08T07:01:20Z
day: '08'
doi: 10.1007/s11433-018-9234-3
extern: '1'
external_id:
arxiv:
- '1812.04460'
intvolume: ' 62'
issue: '2'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.48550/arXiv.1812.04460
month: '10'
oa: 1
oa_version: Preprint
publication: Science China Physics, Mechanics & Astronomy
publication_identifier:
eissn:
- 1869-1927
issn:
- 1674-7348
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Physics and astrophysics of strong magnetic field systems with eXTP
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 62
year: '2018'
...
---
_id: '10626'
abstract:
- lang: eng
text: "Owing to their wide tunability, multiple internal degrees of freedom, and
low disorder, graphene heterostructures are emerging as a promising experimental
platform for fractional quantum Hall (FQH) studies. Here, we report FQH thermal
activation gap measurements in dual graphite-gated monolayer graphene devices
fabricated in an edgeless Corbino geometry. In devices with substrate-induced
sublattice splitting, we find a tunable crossover between single- and multicomponent
FQH states in the zero energy Landau level. Activation gaps in the single-component
regime show excellent agreement with numerical calculations using a single broadening
parameter \r\nΓ≈7.2K. In the first excited Landau level, in contrast, FQH gaps
are strongly influenced by Landau level mixing, and we observe an unexpected valley-ordered
state at integer filling ν=−4."
acknowledgement: We thank Cory Dean, S. Chen, Y. Zeng, M. Yankowitz, and J. Li for
discussing their unpublished data and for sharing the stack inversion technique.
The authors acknowledge further discussions of the results with I. Sodemann, M.
Zaletel, C. Nayak, and J. Jain. A. F. Y., H. P., H. Z., and E. M. S. were supported
by the ARO under awards 69188PHH and MURI W911NF-17-1-0323. A portion of this work
was performed at the National High Magnetic Field Laboratory, which is supported
by National Science Foundation Cooperative Agreement No. DMR-1644779 and the State
of Florida. K. W. and T. T. acknowledge support from the Elemental Strategy Initiative
conducted by the MEXT, Japan, and JSPS KAKENHI Grant No. JP15K21722. E. M. S. acknowledges
the support of the Elings Prize Fellowship in Science of the California Nanosystems
Institute at the University of California, Santa Barbara. A. F. Y. acknowledges
the support of the David and Lucile Packard Foundation.
article_number: '226801'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
- first_name: H.
full_name: Zhou, H.
last_name: Zhou
- first_name: E. M.
full_name: Spanton, E. M.
last_name: Spanton
- first_name: T.
full_name: Taniguchi, T.
last_name: Taniguchi
- first_name: K.
full_name: Watanabe, K.
last_name: Watanabe
- first_name: A. F.
full_name: Young, A. F.
last_name: Young
citation:
ama: Polshyn H, Zhou H, Spanton EM, Taniguchi T, Watanabe K, Young AF. Quantitative
transport measurements of fractional quantum Hall energy gaps in edgeless graphene
devices. Physical Review Letters. 2018;121(22). doi:10.1103/physrevlett.121.226801
apa: Polshyn, H., Zhou, H., Spanton, E. M., Taniguchi, T., Watanabe, K., & Young,
A. F. (2018). Quantitative transport measurements of fractional quantum Hall energy
gaps in edgeless graphene devices. Physical Review Letters. American Physical
Society. https://doi.org/10.1103/physrevlett.121.226801
chicago: Polshyn, Hryhoriy, H. Zhou, E. M. Spanton, T. Taniguchi, K. Watanabe, and
A. F. Young. “Quantitative Transport Measurements of Fractional Quantum Hall Energy
Gaps in Edgeless Graphene Devices.” Physical Review Letters. American Physical
Society, 2018. https://doi.org/10.1103/physrevlett.121.226801.
ieee: H. Polshyn, H. Zhou, E. M. Spanton, T. Taniguchi, K. Watanabe, and A. F. Young,
“Quantitative transport measurements of fractional quantum Hall energy gaps in
edgeless graphene devices,” Physical Review Letters, vol. 121, no. 22.
American Physical Society, 2018.
ista: Polshyn H, Zhou H, Spanton EM, Taniguchi T, Watanabe K, Young AF. 2018. Quantitative
transport measurements of fractional quantum Hall energy gaps in edgeless graphene
devices. Physical Review Letters. 121(22), 226801.
mla: Polshyn, Hryhoriy, et al. “Quantitative Transport Measurements of Fractional
Quantum Hall Energy Gaps in Edgeless Graphene Devices.” Physical Review Letters,
vol. 121, no. 22, 226801, American Physical Society, 2018, doi:10.1103/physrevlett.121.226801.
short: H. Polshyn, H. Zhou, E.M. Spanton, T. Taniguchi, K. Watanabe, A.F. Young,
Physical Review Letters 121 (2018).
date_created: 2022-01-14T12:15:47Z
date_published: 2018-11-28T00:00:00Z
date_updated: 2022-01-14T13:48:35Z
day: '28'
doi: 10.1103/physrevlett.121.226801
extern: '1'
external_id:
arxiv:
- '1805.04199'
intvolume: ' 121'
issue: '22'
keyword:
- general physics and astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1805.04199
month: '11'
oa: 1
oa_version: Preprint
publication: Physical Review Letters
publication_identifier:
eissn:
- 1079-7114
issn:
- 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Quantitative transport measurements of fractional quantum Hall energy gaps
in edgeless graphene devices
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 121
year: '2018'
...
---
_id: '10362'
abstract:
- lang: eng
text: Nuclear pore complexes (NPCs) form gateways that control molecular exchange
between the nucleus and the cytoplasm. They impose a diffusion barrier to macromolecules
and enable the selective transport of nuclear transport receptors with bound cargo.
The underlying mechanisms that establish these permeability properties remain
to be fully elucidated but require unstructured nuclear pore proteins rich in
Phe-Gly (FG)-repeat domains of different types, such as FxFG and GLFG. While physical
modeling and in vitro approaches have provided a framework for explaining how
the FG network contributes to the barrier and transport properties of the NPC,
it remains unknown whether the number and/or the spatial positioning of different
FG-domains along a cylindrical, ∼40 nm diameter transport channel contributes
to their collective properties and function. To begin to answer these questions,
we have used DNA origami to build a cylinder that mimics the dimensions of the
central transport channel and can house a specified number of FG-domains at specific
positions with easily tunable design parameters, such as grafting density and
topology. We find the overall morphology of the FG-domain assemblies to be dependent
on their chemical composition, determined by the type and density of FG-repeat,
and on their architectural confinement provided by the DNA cylinder, largely consistent
with here presented molecular dynamics simulations based on a coarse-grained polymer
model. In addition, high-speed atomic force microscopy reveals local and reversible
FG-domain condensation that transiently occludes the lumen of the DNA central
channel mimics, suggestive of how the NPC might establish its permeability properties.
acknowledgement: We thank J. Edel and members of the Lusk, Lin and Hoogenboom lab
for discussion and acknowledge A. Pyne and R. Thorogate for support carrying out
the AFM experiments. This work was funded by the NIH (R21GM109466 to CPL, CL and
TJM, DP2GM114830 to CL, RO1GM105672 to CPL, and T32GM007223 to PDEF) and the UK
Engineering and Physical Sciences Research Council (EP/L015277/1, EP/L504889/1,
and EP/M028100/1).
article_processing_charge: No
article_type: original
author:
- first_name: Patrick D. Ellis
full_name: Fisher, Patrick D. Ellis
last_name: Fisher
- first_name: Qi
full_name: Shen, Qi
last_name: Shen
- first_name: Bernice
full_name: Akpinar, Bernice
last_name: Akpinar
- first_name: Luke K.
full_name: Davis, Luke K.
last_name: Davis
- first_name: Kenny Kwok Hin
full_name: Chung, Kenny Kwok Hin
last_name: Chung
- first_name: David
full_name: Baddeley, David
last_name: Baddeley
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Thomas J.
full_name: Melia, Thomas J.
last_name: Melia
- first_name: Bart W.
full_name: Hoogenboom, Bart W.
last_name: Hoogenboom
- first_name: Chenxiang
full_name: Lin, Chenxiang
last_name: Lin
- first_name: C. Patrick
full_name: Lusk, C. Patrick
last_name: Lusk
citation:
ama: Fisher PDE, Shen Q, Akpinar B, et al. A Programmable DNA origami platform for
organizing intrinsically disordered nucleoporins within nanopore confinement.
ACS Nano. 2018;12(2):1508-1518. doi:10.1021/acsnano.7b08044
apa: Fisher, P. D. E., Shen, Q., Akpinar, B., Davis, L. K., Chung, K. K. H., Baddeley,
D., … Lusk, C. P. (2018). A Programmable DNA origami platform for organizing intrinsically
disordered nucleoporins within nanopore confinement. ACS Nano. American
Chemical Society. https://doi.org/10.1021/acsnano.7b08044
chicago: Fisher, Patrick D. Ellis, Qi Shen, Bernice Akpinar, Luke K. Davis, Kenny
Kwok Hin Chung, David Baddeley, Anđela Šarić, et al. “A Programmable DNA Origami
Platform for Organizing Intrinsically Disordered Nucleoporins within Nanopore
Confinement.” ACS Nano. American Chemical Society, 2018. https://doi.org/10.1021/acsnano.7b08044.
ieee: P. D. E. Fisher et al., “A Programmable DNA origami platform for organizing
intrinsically disordered nucleoporins within nanopore confinement,” ACS Nano,
vol. 12, no. 2. American Chemical Society, pp. 1508–1518, 2018.
ista: Fisher PDE, Shen Q, Akpinar B, Davis LK, Chung KKH, Baddeley D, Šarić A, Melia
TJ, Hoogenboom BW, Lin C, Lusk CP. 2018. A Programmable DNA origami platform for
organizing intrinsically disordered nucleoporins within nanopore confinement.
ACS Nano. 12(2), 1508–1518.
mla: Fisher, Patrick D. Ellis, et al. “A Programmable DNA Origami Platform for Organizing
Intrinsically Disordered Nucleoporins within Nanopore Confinement.” ACS Nano,
vol. 12, no. 2, American Chemical Society, 2018, pp. 1508–18, doi:10.1021/acsnano.7b08044.
short: P.D.E. Fisher, Q. Shen, B. Akpinar, L.K. Davis, K.K.H. Chung, D. Baddeley,
A. Šarić, T.J. Melia, B.W. Hoogenboom, C. Lin, C.P. Lusk, ACS Nano 12 (2018) 1508–1518.
date_created: 2021-11-26T15:15:00Z
date_published: 2018-01-19T00:00:00Z
date_updated: 2021-11-26T15:57:02Z
day: '19'
doi: 10.1021/acsnano.7b08044
extern: '1'
external_id:
pmid:
- '29350911'
intvolume: ' 12'
issue: '2'
keyword:
- general physics and astronomy
language:
- iso: eng
month: '01'
oa_version: None
page: 1508-1518
pmid: 1
publication: ACS Nano
publication_identifier:
eissn:
- 1936-086X
issn:
- 1936-0851
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: A Programmable DNA origami platform for organizing intrinsically disordered
nucleoporins within nanopore confinement
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 12
year: '2018'
...
---
_id: '8419'
abstract:
- lang: eng
text: "In this survey, we provide a concise introduction to convex billiards and
describe some recent results, obtained by the authors and collaborators, on the
classification of integrable billiards, namely the so-called Birkhoff conjecture.\r\n\r\nThis
article is part of the theme issue ‘Finite dimensional integrable systems: new
trends and methods’."
article_number: '20170419'
article_processing_charge: No
article_type: original
author:
- first_name: Vadim
full_name: Kaloshin, Vadim
id: FE553552-CDE8-11E9-B324-C0EBE5697425
last_name: Kaloshin
orcid: 0000-0002-6051-2628
- first_name: Alfonso
full_name: Sorrentino, Alfonso
last_name: Sorrentino
citation:
ama: 'Kaloshin V, Sorrentino A. On the integrability of Birkhoff billiards. Philosophical
Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.
2018;376(2131). doi:10.1098/rsta.2017.0419'
apa: 'Kaloshin, V., & Sorrentino, A. (2018). On the integrability of Birkhoff
billiards. Philosophical Transactions of the Royal Society A: Mathematical,
Physical and Engineering Sciences. The Royal Society. https://doi.org/10.1098/rsta.2017.0419'
chicago: 'Kaloshin, Vadim, and Alfonso Sorrentino. “On the Integrability of Birkhoff
Billiards.” Philosophical Transactions of the Royal Society A: Mathematical,
Physical and Engineering Sciences. The Royal Society, 2018. https://doi.org/10.1098/rsta.2017.0419.'
ieee: 'V. Kaloshin and A. Sorrentino, “On the integrability of Birkhoff billiards,”
Philosophical Transactions of the Royal Society A: Mathematical, Physical and
Engineering Sciences, vol. 376, no. 2131. The Royal Society, 2018.'
ista: 'Kaloshin V, Sorrentino A. 2018. On the integrability of Birkhoff billiards.
Philosophical Transactions of the Royal Society A: Mathematical, Physical and
Engineering Sciences. 376(2131), 20170419.'
mla: 'Kaloshin, Vadim, and Alfonso Sorrentino. “On the Integrability of Birkhoff
Billiards.” Philosophical Transactions of the Royal Society A: Mathematical,
Physical and Engineering Sciences, vol. 376, no. 2131, 20170419, The Royal
Society, 2018, doi:10.1098/rsta.2017.0419.'
short: 'V. Kaloshin, A. Sorrentino, Philosophical Transactions of the Royal Society
A: Mathematical, Physical and Engineering Sciences 376 (2018).'
date_created: 2020-09-17T10:42:01Z
date_published: 2018-10-28T00:00:00Z
date_updated: 2021-01-12T08:19:09Z
day: '28'
doi: 10.1098/rsta.2017.0419
extern: '1'
intvolume: ' 376'
issue: '2131'
keyword:
- General Engineering
- General Physics and Astronomy
- General Mathematics
language:
- iso: eng
month: '10'
oa_version: None
publication: 'Philosophical Transactions of the Royal Society A: Mathematical, Physical
and Engineering Sciences'
publication_identifier:
issn:
- 1364-503X
- 1471-2962
publication_status: published
publisher: The Royal Society
quality_controlled: '1'
status: public
title: On the integrability of Birkhoff billiards
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 376
year: '2018'
...
---
_id: '8420'
abstract:
- lang: eng
text: We show that in the space of all convex billiard boundaries, the set of boundaries
with rational caustics is dense. More precisely, the set of billiard boundaries
with caustics of rotation number 1/q is polynomially sense in the smooth case,
and exponentially dense in the analytic case.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Vadim
full_name: Kaloshin, Vadim
id: FE553552-CDE8-11E9-B324-C0EBE5697425
last_name: Kaloshin
orcid: 0000-0002-6051-2628
- first_name: Ke
full_name: Zhang, Ke
last_name: Zhang
citation:
ama: Kaloshin V, Zhang K. Density of convex billiards with rational caustics. Nonlinearity.
2018;31(11):5214-5234. doi:10.1088/1361-6544/aadc12
apa: Kaloshin, V., & Zhang, K. (2018). Density of convex billiards with rational
caustics. Nonlinearity. IOP Publishing. https://doi.org/10.1088/1361-6544/aadc12
chicago: Kaloshin, Vadim, and Ke Zhang. “Density of Convex Billiards with Rational
Caustics.” Nonlinearity. IOP Publishing, 2018. https://doi.org/10.1088/1361-6544/aadc12.
ieee: V. Kaloshin and K. Zhang, “Density of convex billiards with rational caustics,”
Nonlinearity, vol. 31, no. 11. IOP Publishing, pp. 5214–5234, 2018.
ista: Kaloshin V, Zhang K. 2018. Density of convex billiards with rational caustics.
Nonlinearity. 31(11), 5214–5234.
mla: Kaloshin, Vadim, and Ke Zhang. “Density of Convex Billiards with Rational Caustics.”
Nonlinearity, vol. 31, no. 11, IOP Publishing, 2018, pp. 5214–34, doi:10.1088/1361-6544/aadc12.
short: V. Kaloshin, K. Zhang, Nonlinearity 31 (2018) 5214–5234.
date_created: 2020-09-17T10:42:09Z
date_published: 2018-10-15T00:00:00Z
date_updated: 2021-01-12T08:19:10Z
day: '15'
doi: 10.1088/1361-6544/aadc12
extern: '1'
external_id:
arxiv:
- '1706.07968'
intvolume: ' 31'
issue: '11'
keyword:
- Mathematical Physics
- General Physics and Astronomy
- Applied Mathematics
- Statistical and Nonlinear Physics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1706.07968
month: '10'
oa: 1
oa_version: Preprint
page: 5214-5234
publication: Nonlinearity
publication_identifier:
issn:
- 0951-7715
- 1361-6544
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
status: public
title: Density of convex billiards with rational caustics
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 31
year: '2018'
...
---
_id: '14004'
abstract:
- lang: eng
text: High-harmonic spectroscopy driven by circularly polarized laser pulses and
their counterrotating second harmonic is a new branch of attosecond science which
currently lacks quantitative interpretations. We extend this technique to the
midinfrared regime and record detailed high-harmonic spectra of several rare-gas
atoms. These results are compared with the solution of the Schrödinger equation
in three dimensions and calculations based on the strong-field approximation that
incorporate accurate scattering-wave recombination matrix elements. A quantum-orbit
analysis of these results provides a transparent interpretation of the measured
intensity ratios of symmetry-allowed neighboring harmonics in terms of (i) a set
of propensity rules related to the angular momentum of the atomic orbitals, (ii)
atom-specific matrix elements related to their electronic structure, and (iii)
the interference of the emissions associated with electrons in orbitals corotating
or counterrotating with the laser fields. These results provide the foundation
for a quantitative understanding of bicircular high-harmonic spectroscopy.
article_number: '203201'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Denitsa Rangelova
full_name: Baykusheva, Denitsa Rangelova
id: 71b4d059-2a03-11ee-914d-dfa3beed6530
last_name: Baykusheva
- first_name: Simon
full_name: Brennecke, Simon
last_name: Brennecke
- first_name: Manfred
full_name: Lein, Manfred
last_name: Lein
- first_name: Hans Jakob
full_name: Wörner, Hans Jakob
last_name: Wörner
citation:
ama: Baykusheva DR, Brennecke S, Lein M, Wörner HJ. Signatures of electronic structure
in bicircular high-harmonic spectroscopy. Physical Review Letters. 2017;119(20).
doi:10.1103/physrevlett.119.203201
apa: Baykusheva, D. R., Brennecke, S., Lein, M., & Wörner, H. J. (2017). Signatures
of electronic structure in bicircular high-harmonic spectroscopy. Physical
Review Letters. American Physical Society. https://doi.org/10.1103/physrevlett.119.203201
chicago: Baykusheva, Denitsa Rangelova, Simon Brennecke, Manfred Lein, and Hans
Jakob Wörner. “Signatures of Electronic Structure in Bicircular High-Harmonic
Spectroscopy.” Physical Review Letters. American Physical Society, 2017.
https://doi.org/10.1103/physrevlett.119.203201.
ieee: D. R. Baykusheva, S. Brennecke, M. Lein, and H. J. Wörner, “Signatures of
electronic structure in bicircular high-harmonic spectroscopy,” Physical Review
Letters, vol. 119, no. 20. American Physical Society, 2017.
ista: Baykusheva DR, Brennecke S, Lein M, Wörner HJ. 2017. Signatures of electronic
structure in bicircular high-harmonic spectroscopy. Physical Review Letters. 119(20),
203201.
mla: Baykusheva, Denitsa Rangelova, et al. “Signatures of Electronic Structure in
Bicircular High-Harmonic Spectroscopy.” Physical Review Letters, vol. 119,
no. 20, 203201, American Physical Society, 2017, doi:10.1103/physrevlett.119.203201.
short: D.R. Baykusheva, S. Brennecke, M. Lein, H.J. Wörner, Physical Review Letters
119 (2017).
date_created: 2023-08-10T06:35:51Z
date_published: 2017-11-17T00:00:00Z
date_updated: 2023-08-22T08:21:10Z
day: '17'
doi: 10.1103/physrevlett.119.203201
extern: '1'
external_id:
arxiv:
- '1710.04474'
intvolume: ' 119'
issue: '20'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1710.04474
month: '11'
oa: 1
oa_version: Preprint
publication: Physical Review Letters
publication_identifier:
eissn:
- 1079-7114
issn:
- 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Signatures of electronic structure in bicircular high-harmonic spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 119
year: '2017'
...
---
_id: '14005'
abstract:
- lang: eng
text: Strong-field photoelectron holography and laser-induced electron diffraction
(LIED) are two powerful emerging methods for probing the ultrafast dynamics of
molecules. However, both of them have remained restricted to static systems and
to nuclear dynamics induced by strong-field ionization. Here we extend these promising
methods to image purely electronic valence-shell dynamics in molecules using photoelectron
holography. In the same experiment, we use LIED and photoelectron holography simultaneously,
to observe coupled electronic-rotational dynamics taking place on similar timescales.
These results offer perspectives for imaging ultrafast dynamics of molecules on
femtosecond to attosecond timescales.
article_number: '15651'
article_processing_charge: No
article_type: original
author:
- first_name: Samuel G.
full_name: Walt, Samuel G.
last_name: Walt
- first_name: Niraghatam
full_name: Bhargava Ram, Niraghatam
last_name: Bhargava Ram
- first_name: Marcos
full_name: Atala, Marcos
last_name: Atala
- first_name: Nikolay I
full_name: Shvetsov-Shilovski, Nikolay I
last_name: Shvetsov-Shilovski
- first_name: Aaron
full_name: von Conta, Aaron
last_name: von Conta
- first_name: Denitsa Rangelova
full_name: Baykusheva, Denitsa Rangelova
id: 71b4d059-2a03-11ee-914d-dfa3beed6530
last_name: Baykusheva
- first_name: Manfred
full_name: Lein, Manfred
last_name: Lein
- first_name: Hans Jakob
full_name: Wörner, Hans Jakob
last_name: Wörner
citation:
ama: Walt SG, Bhargava Ram N, Atala M, et al. Dynamics of valence-shell electrons
and nuclei probed by strong-field holography and rescattering. Nature Communications.
2017;8. doi:10.1038/ncomms15651
apa: Walt, S. G., Bhargava Ram, N., Atala, M., Shvetsov-Shilovski, N. I., von Conta,
A., Baykusheva, D. R., … Wörner, H. J. (2017). Dynamics of valence-shell electrons
and nuclei probed by strong-field holography and rescattering. Nature Communications.
Springer Nature. https://doi.org/10.1038/ncomms15651
chicago: Walt, Samuel G., Niraghatam Bhargava Ram, Marcos Atala, Nikolay I Shvetsov-Shilovski,
Aaron von Conta, Denitsa Rangelova Baykusheva, Manfred Lein, and Hans Jakob Wörner.
“Dynamics of Valence-Shell Electrons and Nuclei Probed by Strong-Field Holography
and Rescattering.” Nature Communications. Springer Nature, 2017. https://doi.org/10.1038/ncomms15651.
ieee: S. G. Walt et al., “Dynamics of valence-shell electrons and nuclei
probed by strong-field holography and rescattering,” Nature Communications,
vol. 8. Springer Nature, 2017.
ista: Walt SG, Bhargava Ram N, Atala M, Shvetsov-Shilovski NI, von Conta A, Baykusheva
DR, Lein M, Wörner HJ. 2017. Dynamics of valence-shell electrons and nuclei probed
by strong-field holography and rescattering. Nature Communications. 8, 15651.
mla: Walt, Samuel G., et al. “Dynamics of Valence-Shell Electrons and Nuclei Probed
by Strong-Field Holography and Rescattering.” Nature Communications, vol.
8, 15651, Springer Nature, 2017, doi:10.1038/ncomms15651.
short: S.G. Walt, N. Bhargava Ram, M. Atala, N.I. Shvetsov-Shilovski, A. von Conta,
D.R. Baykusheva, M. Lein, H.J. Wörner, Nature Communications 8 (2017).
date_created: 2023-08-10T06:36:09Z
date_published: 2017-06-15T00:00:00Z
date_updated: 2023-08-22T08:26:06Z
day: '15'
doi: 10.1038/ncomms15651
extern: '1'
external_id:
pmid:
- '28643771'
intvolume: ' 8'
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1038/ncomms15651
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
eissn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dynamics of valence-shell electrons and nuclei probed by strong-field holography
and rescattering
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2017'
...
---
_id: '14006'
abstract:
- lang: eng
text: We present a theoretical formalism for the calculation of attosecond delays
in molecular photoionization. It is shown how delays relevant to one-photon-ionization,
also known as Eisenbud-Wigner-Smith delays, can be obtained from the complex dipole
matrix elements provided by molecular quantum scattering theory. These results
are used to derive formulae for the delays measured by two-photon attosecond interferometry
based on an attosecond pulse train and a dressing femtosecond infrared pulse.
These effective delays are first expressed in the molecular frame where maximal
information about the molecular photoionization dynamics is available. The effects
of averaging over the emission direction of the electron and the molecular orientation
are introduced analytically. We illustrate this general formalism for the case
of two polyatomic molecules. N2O serves as an example of a polar linear molecule
characterized by complex photoionization dynamics resulting from the presence
of molecular shape resonances. H2O illustrates the case of a non-linear molecule
with comparably simple photoionization dynamics resulting from a flat continuum.
Our theory establishes the foundation for interpreting measurements of the photoionization
dynamics of all molecules by attosecond metrology.
article_number: '124306'
article_processing_charge: No
article_type: original
author:
- first_name: Denitsa Rangelova
full_name: Baykusheva, Denitsa Rangelova
id: 71b4d059-2a03-11ee-914d-dfa3beed6530
last_name: Baykusheva
- first_name: Hans Jakob
full_name: Wörner, Hans Jakob
last_name: Wörner
citation:
ama: Baykusheva DR, Wörner HJ. Theory of attosecond delays in molecular photoionization.
The Journal of Chemical Physics. 2017;146(12). doi:10.1063/1.4977933
apa: Baykusheva, D. R., & Wörner, H. J. (2017). Theory of attosecond delays
in molecular photoionization. The Journal of Chemical Physics. AIP Publishing.
https://doi.org/10.1063/1.4977933
chicago: Baykusheva, Denitsa Rangelova, and Hans Jakob Wörner. “Theory of Attosecond
Delays in Molecular Photoionization.” The Journal of Chemical Physics.
AIP Publishing, 2017. https://doi.org/10.1063/1.4977933.
ieee: D. R. Baykusheva and H. J. Wörner, “Theory of attosecond delays in molecular
photoionization,” The Journal of Chemical Physics, vol. 146, no. 12. AIP
Publishing, 2017.
ista: Baykusheva DR, Wörner HJ. 2017. Theory of attosecond delays in molecular photoionization.
The Journal of Chemical Physics. 146(12), 124306.
mla: Baykusheva, Denitsa Rangelova, and Hans Jakob Wörner. “Theory of Attosecond
Delays in Molecular Photoionization.” The Journal of Chemical Physics,
vol. 146, no. 12, 124306, AIP Publishing, 2017, doi:10.1063/1.4977933.
short: D.R. Baykusheva, H.J. Wörner, The Journal of Chemical Physics 146 (2017).
date_created: 2023-08-10T06:36:19Z
date_published: 2017-03-28T00:00:00Z
date_updated: 2023-08-22T08:30:59Z
day: '28'
doi: 10.1063/1.4977933
extern: '1'
external_id:
pmid:
- '28388142'
intvolume: ' 146'
issue: '12'
keyword:
- Physical and Theoretical Chemistry
- General Physics and Astronomy
language:
- iso: eng
month: '03'
oa_version: None
pmid: 1
publication: The Journal of Chemical Physics
publication_identifier:
eissn:
- 1089-7690
issn:
- 0021-9606
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Theory of attosecond delays in molecular photoionization
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 146
year: '2017'
...
---
_id: '14031'
abstract:
- lang: eng
text: High-harmonic spectroscopy driven by circularly polarized laser pulses and
their counterrotating second harmonic is a new branch of attosecond science which
currently lacks quantitative interpretations. We extend this technique to the
midinfrared regime and record detailed high-harmonic spectra of several rare-gas
atoms. These results are compared with the solution of the Schrödinger equation
in three dimensions and calculations based on the strong-field approximation that
incorporate accurate scattering-wave recombination matrix elements. A quantum-orbit
analysis of these results provides a transparent interpretation of the measured
intensity ratios of symmetry-allowed neighboring harmonics in terms of (i) a set
of propensity rules related to the angular momentum of the atomic orbitals, (ii)
atom-specific matrix elements related to their electronic structure, and (iii)
the interference of the emissions associated with electrons in orbitals corotating
or counterrotating with the laser fields. These results provide the foundation
for a quantitative understanding of bicircular high-harmonic spectroscopy.
article_number: '203201'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Denitsa Rangelova
full_name: Baykusheva, Denitsa Rangelova
id: 71b4d059-2a03-11ee-914d-dfa3beed6530
last_name: Baykusheva
- first_name: Simon
full_name: Brennecke, Simon
last_name: Brennecke
- first_name: Manfred
full_name: Lein, Manfred
last_name: Lein
- first_name: Hans Jakob
full_name: Wörner, Hans Jakob
last_name: Wörner
citation:
ama: Baykusheva DR, Brennecke S, Lein M, Wörner HJ. Signatures of electronic structure
in bicircular high-harmonic spectroscopy. Physical Review Letters. 2017;119(20).
doi:10.1103/physrevlett.119.203201
apa: Baykusheva, D. R., Brennecke, S., Lein, M., & Wörner, H. J. (2017). Signatures
of electronic structure in bicircular high-harmonic spectroscopy. Physical
Review Letters. American Physical Society. https://doi.org/10.1103/physrevlett.119.203201
chicago: Baykusheva, Denitsa Rangelova, Simon Brennecke, Manfred Lein, and Hans
Jakob Wörner. “Signatures of Electronic Structure in Bicircular High-Harmonic
Spectroscopy.” Physical Review Letters. American Physical Society, 2017.
https://doi.org/10.1103/physrevlett.119.203201.
ieee: D. R. Baykusheva, S. Brennecke, M. Lein, and H. J. Wörner, “Signatures of
electronic structure in bicircular high-harmonic spectroscopy,” Physical Review
Letters, vol. 119, no. 20. American Physical Society, 2017.
ista: Baykusheva DR, Brennecke S, Lein M, Wörner HJ. 2017. Signatures of electronic
structure in bicircular high-harmonic spectroscopy. Physical Review Letters. 119(20),
203201.
mla: Baykusheva, Denitsa Rangelova, et al. “Signatures of Electronic Structure in
Bicircular High-Harmonic Spectroscopy.” Physical Review Letters, vol. 119,
no. 20, 203201, American Physical Society, 2017, doi:10.1103/physrevlett.119.203201.
short: D.R. Baykusheva, S. Brennecke, M. Lein, H.J. Wörner, Physical Review Letters
119 (2017).
date_created: 2023-08-10T06:48:12Z
date_published: 2017-11-17T00:00:00Z
date_updated: 2023-08-22T06:48:28Z
day: '17'
doi: 10.1103/physrevlett.119.203201
extern: '1'
external_id:
arxiv:
- '1710.04474'
pmid:
- '29219334'
intvolume: ' 119'
issue: '20'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1710.04474
month: '11'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
eissn:
- 1079-7114
issn:
- 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Signatures of electronic structure in bicircular high-harmonic spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 119
year: '2017'
...
---
_id: '11065'
abstract:
- lang: eng
text: Premature aging disorders provide an opportunity to study the mechanisms that
drive aging. In Hutchinson-Gilford progeria syndrome (HGPS), a mutant form of
the nuclear scaffold protein lamin A distorts nuclei and sequesters nuclear proteins.
We sought to investigate protein homeostasis in this disease. Here, we report
a widespread increase in protein turnover in HGPS-derived cells compared to normal
cells. We determine that global protein synthesis is elevated as a consequence
of activated nucleoli and enhanced ribosome biogenesis in HGPS-derived fibroblasts.
Depleting normal lamin A or inducing mutant lamin A expression are each sufficient
to drive nucleolar expansion. We further show that nucleolar size correlates with
donor age in primary fibroblasts derived from healthy individuals and that ribosomal
RNA production increases with age, indicating that nucleolar size and activity
can serve as aging biomarkers. While limiting ribosome biogenesis extends lifespan
in several systems, we show that increased ribosome biogenesis and activity are
a hallmark of premature aging.
article_number: '328'
article_processing_charge: No
article_type: original
author:
- first_name: Abigail
full_name: Buchwalter, Abigail
last_name: Buchwalter
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Buchwalter A, Hetzer M. Nucleolar expansion and elevated protein translation
in premature aging. Nature Communications. 2017;8. doi:10.1038/s41467-017-00322-z
apa: Buchwalter, A., & Hetzer, M. (2017). Nucleolar expansion and elevated protein
translation in premature aging. Nature Communications. Springer Nature.
https://doi.org/10.1038/s41467-017-00322-z
chicago: Buchwalter, Abigail, and Martin Hetzer. “Nucleolar Expansion and Elevated
Protein Translation in Premature Aging.” Nature Communications. Springer
Nature, 2017. https://doi.org/10.1038/s41467-017-00322-z.
ieee: A. Buchwalter and M. Hetzer, “Nucleolar expansion and elevated protein translation
in premature aging,” Nature Communications, vol. 8. Springer Nature, 2017.
ista: Buchwalter A, Hetzer M. 2017. Nucleolar expansion and elevated protein translation
in premature aging. Nature Communications. 8, 328.
mla: Buchwalter, Abigail, and Martin Hetzer. “Nucleolar Expansion and Elevated Protein
Translation in Premature Aging.” Nature Communications, vol. 8, 328, Springer
Nature, 2017, doi:10.1038/s41467-017-00322-z.
short: A. Buchwalter, M. Hetzer, Nature Communications 8 (2017).
date_created: 2022-04-07T07:45:50Z
date_published: 2017-08-30T00:00:00Z
date_updated: 2024-10-14T11:20:12Z
day: '30'
doi: 10.1038/s41467-017-00322-z
extern: '1'
external_id:
pmid:
- '28855503'
intvolume: ' 8'
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1038/s41467-017-00322-z
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nucleolar expansion and elevated protein translation in premature aging
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2017'
...
---
_id: '14010'
abstract:
- lang: eng
text: We report measurements of energy-dependent attosecond photoionization delays
between the two outer-most valence shells of N2O and H2O. The combination of single-shot
signal referencing with the use of different metal foils to filter the attosecond
pulse train enables us to extract delays from congested spectra. Remarkably large
delays up to 160 as are observed in N2O, whereas the delays in H2O are all smaller
than 50 as in the photon-energy range of 20-40 eV. These results are interpreted
by developing a theory of molecular photoionization delays. The long delays measured
in N2O are shown to reflect the population of molecular shape resonances that
trap the photoelectron for a duration of up to ∼110 as. The unstructured continua
of H2O result in much smaller delays at the same photon energies. Our experimental
and theoretical methods make the study of molecular attosecond photoionization
dynamics accessible.
article_number: '093001'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Martin
full_name: Huppert, Martin
last_name: Huppert
- first_name: Inga
full_name: Jordan, Inga
last_name: Jordan
- first_name: Denitsa Rangelova
full_name: Baykusheva, Denitsa Rangelova
id: 71b4d059-2a03-11ee-914d-dfa3beed6530
last_name: Baykusheva
- first_name: Aaron
full_name: von Conta, Aaron
last_name: von Conta
- first_name: Hans Jakob
full_name: Wörner, Hans Jakob
last_name: Wörner
citation:
ama: Huppert M, Jordan I, Baykusheva DR, von Conta A, Wörner HJ. Attosecond delays
in molecular photoionization. Physical Review Letters. 2016;117(9). doi:10.1103/physrevlett.117.093001
apa: Huppert, M., Jordan, I., Baykusheva, D. R., von Conta, A., & Wörner, H.
J. (2016). Attosecond delays in molecular photoionization. Physical Review
Letters. American Physical Society. https://doi.org/10.1103/physrevlett.117.093001
chicago: Huppert, Martin, Inga Jordan, Denitsa Rangelova Baykusheva, Aaron von Conta,
and Hans Jakob Wörner. “Attosecond Delays in Molecular Photoionization.” Physical
Review Letters. American Physical Society, 2016. https://doi.org/10.1103/physrevlett.117.093001.
ieee: M. Huppert, I. Jordan, D. R. Baykusheva, A. von Conta, and H. J. Wörner, “Attosecond
delays in molecular photoionization,” Physical Review Letters, vol. 117,
no. 9. American Physical Society, 2016.
ista: Huppert M, Jordan I, Baykusheva DR, von Conta A, Wörner HJ. 2016. Attosecond
delays in molecular photoionization. Physical Review Letters. 117(9), 093001.
mla: Huppert, Martin, et al. “Attosecond Delays in Molecular Photoionization.” Physical
Review Letters, vol. 117, no. 9, 093001, American Physical Society, 2016,
doi:10.1103/physrevlett.117.093001.
short: M. Huppert, I. Jordan, D.R. Baykusheva, A. von Conta, H.J. Wörner, Physical
Review Letters 117 (2016).
date_created: 2023-08-10T06:37:07Z
date_published: 2016-08-26T00:00:00Z
date_updated: 2023-08-22T08:42:50Z
day: '26'
doi: 10.1103/physrevlett.117.093001
extern: '1'
external_id:
arxiv:
- '1607.07435'
pmid:
- '27610849'
intvolume: ' 117'
issue: '9'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1607.07435
month: '08'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
eissn:
- 1079-7114
issn:
- 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Attosecond delays in molecular photoionization
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 117
year: '2016'
...
---
_id: '14011'
abstract:
- lang: eng
text: We introduce bicircular high-harmonic spectroscopy as a new method to probe
dynamical symmetries of atoms and molecules and their evolution in time. Our approach
is based on combining a circularly polarized femtosecond fundamental field of
frequency ω with its counterrotating second harmonic 2ω. We demonstrate the ability
of bicircular high-harmonic spectroscopy to characterize the orbital angular momentum
symmetry of atomic orbitals. We further show that breaking the threefold rotational
symmetry of the generating medium-at the level of either the ensemble or that
of a single molecule-results in the emission of the otherwise parity-forbidden
frequencies 3qω (q∈N), which provide a background-free probe of dynamical molecular
symmetries.
article_number: '123001'
article_processing_charge: No
article_type: original
author:
- first_name: Denitsa Rangelova
full_name: Baykusheva, Denitsa Rangelova
id: 71b4d059-2a03-11ee-914d-dfa3beed6530
last_name: Baykusheva
- first_name: Md Sabbir
full_name: Ahsan, Md Sabbir
last_name: Ahsan
- first_name: 'Nan'
full_name: Lin, Nan
last_name: Lin
- first_name: Hans Jakob
full_name: Wörner, Hans Jakob
last_name: Wörner
citation:
ama: Baykusheva DR, Ahsan MS, Lin N, Wörner HJ. Bicircular high-harmonic spectroscopy
reveals dynamical symmetries of atoms and molecules. Physical Review Letters.
2016;116(12). doi:10.1103/physrevlett.116.123001
apa: Baykusheva, D. R., Ahsan, M. S., Lin, N., & Wörner, H. J. (2016). Bicircular
high-harmonic spectroscopy reveals dynamical symmetries of atoms and molecules.
Physical Review Letters. American Physical Society. https://doi.org/10.1103/physrevlett.116.123001
chicago: Baykusheva, Denitsa Rangelova, Md Sabbir Ahsan, Nan Lin, and Hans Jakob
Wörner. “Bicircular High-Harmonic Spectroscopy Reveals Dynamical Symmetries of
Atoms and Molecules.” Physical Review Letters. American Physical Society,
2016. https://doi.org/10.1103/physrevlett.116.123001.
ieee: D. R. Baykusheva, M. S. Ahsan, N. Lin, and H. J. Wörner, “Bicircular high-harmonic
spectroscopy reveals dynamical symmetries of atoms and molecules,” Physical
Review Letters, vol. 116, no. 12. American Physical Society, 2016.
ista: Baykusheva DR, Ahsan MS, Lin N, Wörner HJ. 2016. Bicircular high-harmonic
spectroscopy reveals dynamical symmetries of atoms and molecules. Physical Review
Letters. 116(12), 123001.
mla: Baykusheva, Denitsa Rangelova, et al. “Bicircular High-Harmonic Spectroscopy
Reveals Dynamical Symmetries of Atoms and Molecules.” Physical Review Letters,
vol. 116, no. 12, 123001, American Physical Society, 2016, doi:10.1103/physrevlett.116.123001.
short: D.R. Baykusheva, M.S. Ahsan, N. Lin, H.J. Wörner, Physical Review Letters
116 (2016).
date_created: 2023-08-10T06:37:16Z
date_published: 2016-03-25T00:00:00Z
date_updated: 2023-08-22T08:44:10Z
day: '25'
doi: 10.1103/physrevlett.116.123001
extern: '1'
external_id:
pmid:
- '27058077'
intvolume: ' 116'
issue: '12'
keyword:
- General Physics and Astronomy
language:
- iso: eng
month: '03'
oa_version: None
pmid: 1
publication: Physical Review Letters
publication_identifier:
eissn:
- 1079-7114
issn:
- 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Bicircular high-harmonic spectroscopy reveals dynamical symmetries of atoms
and molecules
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 116
year: '2016'
...
---
_id: '11072'
abstract:
- lang: eng
text: "Spatiotemporal activation of RhoA and actomyosin contraction underpins cellular
adhesion and division. Loss of cell–cell adhesion and chromosomal instability
are cardinal events that drive tumour progression. Here, we show that p120-catenin
(p120) not only controls cell–cell adhesion, but also acts as a critical regulator
of cytokinesis. We find that p120 regulates actomyosin contractility through concomitant
binding to RhoA and the centralspindlin component MKLP1, independent of cadherin
association. In anaphase, p120 is enriched at the cleavage furrow where it binds
MKLP1 to spatially control RhoA GTPase cycling. Binding of p120 to MKLP1 during
cytokinesis depends on the N-terminal coiled-coil domain of p120 isoform 1A. Importantly,
clinical data show that loss of p120 expression is a common event in breast cancer
that strongly correlates with multinucleation and adverse patient survival. In
summary, our study identifies p120 loss as a driver event of chromosomal instability
in cancer.\r\n"
article_number: '13874'
article_processing_charge: No
article_type: original
author:
- first_name: Robert A.H.
full_name: van de Ven, Robert A.H.
last_name: van de Ven
- first_name: Jolien S.
full_name: de Groot, Jolien S.
last_name: de Groot
- first_name: Danielle
full_name: Park, Danielle
last_name: Park
- first_name: Robert
full_name: van Domselaar, Robert
last_name: van Domselaar
- first_name: Danielle
full_name: de Jong, Danielle
last_name: de Jong
- first_name: Karoly
full_name: Szuhai, Karoly
last_name: Szuhai
- first_name: Elsken
full_name: van der Wall, Elsken
last_name: van der Wall
- first_name: Oscar M.
full_name: Rueda, Oscar M.
last_name: Rueda
- first_name: H. Raza
full_name: Ali, H. Raza
last_name: Ali
- first_name: Carlos
full_name: Caldas, Carlos
last_name: Caldas
- first_name: Paul J.
full_name: van Diest, Paul J.
last_name: van Diest
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Erik
full_name: Sahai, Erik
last_name: Sahai
- first_name: Patrick W.B.
full_name: Derksen, Patrick W.B.
last_name: Derksen
citation:
ama: van de Ven RAH, de Groot JS, Park D, et al. p120-catenin prevents multinucleation
through control of MKLP1-dependent RhoA activity during cytokinesis. Nature
Communications. 2016;7. doi:10.1038/ncomms13874
apa: van de Ven, R. A. H., de Groot, J. S., Park, D., van Domselaar, R., de Jong,
D., Szuhai, K., … Derksen, P. W. B. (2016). p120-catenin prevents multinucleation
through control of MKLP1-dependent RhoA activity during cytokinesis. Nature
Communications. Springer Nature. https://doi.org/10.1038/ncomms13874
chicago: Ven, Robert A.H. van de, Jolien S. de Groot, Danielle Park, Robert van
Domselaar, Danielle de Jong, Karoly Szuhai, Elsken van der Wall, et al. “P120-Catenin
Prevents Multinucleation through Control of MKLP1-Dependent RhoA Activity during
Cytokinesis.” Nature Communications. Springer Nature, 2016. https://doi.org/10.1038/ncomms13874.
ieee: R. A. H. van de Ven et al., “p120-catenin prevents multinucleation
through control of MKLP1-dependent RhoA activity during cytokinesis,” Nature
Communications, vol. 7. Springer Nature, 2016.
ista: van de Ven RAH, de Groot JS, Park D, van Domselaar R, de Jong D, Szuhai K,
van der Wall E, Rueda OM, Ali HR, Caldas C, van Diest PJ, Hetzer M, Sahai E, Derksen
PWB. 2016. p120-catenin prevents multinucleation through control of MKLP1-dependent
RhoA activity during cytokinesis. Nature Communications. 7, 13874.
mla: van de Ven, Robert A. H., et al. “P120-Catenin Prevents Multinucleation through
Control of MKLP1-Dependent RhoA Activity during Cytokinesis.” Nature Communications,
vol. 7, 13874, Springer Nature, 2016, doi:10.1038/ncomms13874.
short: R.A.H. van de Ven, J.S. de Groot, D. Park, R. van Domselaar, D. de Jong,
K. Szuhai, E. van der Wall, O.M. Rueda, H.R. Ali, C. Caldas, P.J. van Diest, M.
Hetzer, E. Sahai, P.W.B. Derksen, Nature Communications 7 (2016).
date_created: 2022-04-07T07:48:34Z
date_published: 2016-12-22T00:00:00Z
date_updated: 2022-07-18T08:34:32Z
day: '22'
doi: 10.1038/ncomms13874
extern: '1'
external_id:
pmid:
- '28004812'
intvolume: ' 7'
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1038/ncomms13874
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
link:
- relation: erratum
url: https://doi.org/10.1038/ncomms16030
scopus_import: '1'
status: public
title: p120-catenin prevents multinucleation through control of MKLP1-dependent RhoA
activity during cytokinesis
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 7
year: '2016'
...
---
_id: '10376'
abstract:
- lang: eng
text: Nucleation processes are at the heart of a large number of phenomena, from
cloud formation to protein crystallization. A recently emerging area where nucleation
is highly relevant is the initiation of filamentous protein self-assembly, a process
that has broad implications in many research areas ranging from medicine to nanotechnology.
As such, spontaneous nucleation of protein fibrils has received much attention
in recent years with many theoretical and experimental studies focusing on the
underlying physical principles. In this paper we make a step forward in this direction
and explore the early time behaviour of filamentous protein growth in the context
of nucleation theory. We first provide an overview of the thermodynamics and kinetics
of spontaneous nucleation of protein filaments in the presence of one relevant
degree of freedom, namely the cluster size. In this case, we review how key kinetic
observables, such as the reaction order of spontaneous nucleation, are directly
related to the physical size of the critical nucleus. We then focus on the increasingly
prominent case of filament nucleation that includes a conformational conversion
of the nucleating building-block as an additional slow step in the nucleation
process. Using computer simulations, we study the concentration dependence of
the nucleation rate. We find that, under these circumstances, the reaction order
of spontaneous nucleation with respect to the free monomer does no longer relate
to the overall physical size of the nucleating aggregate but rather to the portion
of the aggregate that actively participates in the conformational conversion.
Our results thus provide a novel interpretation of the common kinetic descriptors
of protein filament formation, including the reaction order of the nucleation
step or the scaling exponent of lag times, and put into perspective current theoretical
descriptions of protein aggregation.
acknowledgement: We acknowledge support from the Human Frontier Science Program and
Emmanuel College (A.Š.), St John’s and Peterhouse Colleges (T.C.T.M.), the Swiss
National Science Foundation (T.C.T.M.), the Biotechnology and Biological Sciences
Research Council (T.P.J.K.), the Frances and Augustus Newman Foundation (T.P.J.K.),
the European Research Council (T.C.T.M., T.P.J.K., and D.F.), and the Engineering
and Physical Sciences Research Council (D.F.).
article_number: '211926'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Thomas C. T.
full_name: Michaels, Thomas C. T.
last_name: Michaels
- first_name: Alessio
full_name: Zaccone, Alessio
last_name: Zaccone
- first_name: Tuomas P. J.
full_name: Knowles, Tuomas P. J.
last_name: Knowles
- first_name: Daan
full_name: Frenkel, Daan
last_name: Frenkel
citation:
ama: 'Šarić A, Michaels TCT, Zaccone A, Knowles TPJ, Frenkel D. Kinetics of spontaneous
filament nucleation via oligomers: Insights from theory and simulation. The
Journal of Chemical Physics. 2016;145(21). doi:10.1063/1.4965040'
apa: 'Šarić, A., Michaels, T. C. T., Zaccone, A., Knowles, T. P. J., & Frenkel,
D. (2016). Kinetics of spontaneous filament nucleation via oligomers: Insights
from theory and simulation. The Journal of Chemical Physics. American Institute
of Physics. https://doi.org/10.1063/1.4965040'
chicago: 'Šarić, Anđela, Thomas C. T. Michaels, Alessio Zaccone, Tuomas P. J. Knowles,
and Daan Frenkel. “Kinetics of Spontaneous Filament Nucleation via Oligomers:
Insights from Theory and Simulation.” The Journal of Chemical Physics.
American Institute of Physics, 2016. https://doi.org/10.1063/1.4965040.'
ieee: 'A. Šarić, T. C. T. Michaels, A. Zaccone, T. P. J. Knowles, and D. Frenkel,
“Kinetics of spontaneous filament nucleation via oligomers: Insights from theory
and simulation,” The Journal of Chemical Physics, vol. 145, no. 21. American
Institute of Physics, 2016.'
ista: 'Šarić A, Michaels TCT, Zaccone A, Knowles TPJ, Frenkel D. 2016. Kinetics
of spontaneous filament nucleation via oligomers: Insights from theory and simulation.
The Journal of Chemical Physics. 145(21), 211926.'
mla: 'Šarić, Anđela, et al. “Kinetics of Spontaneous Filament Nucleation via Oligomers:
Insights from Theory and Simulation.” The Journal of Chemical Physics,
vol. 145, no. 21, 211926, American Institute of Physics, 2016, doi:10.1063/1.4965040.'
short: A. Šarić, T.C.T. Michaels, A. Zaccone, T.P.J. Knowles, D. Frenkel, The Journal
of Chemical Physics 145 (2016).
date_created: 2021-11-29T10:01:57Z
date_published: 2016-12-01T00:00:00Z
date_updated: 2021-11-29T10:33:11Z
day: '01'
doi: 10.1063/1.4965040
extern: '1'
external_id:
arxiv:
- '1610.02320'
pmid:
- '28799382'
intvolume: ' 145'
issue: '21'
keyword:
- physical and theoretical chemistry
- general physics and astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1610.02320
month: '12'
oa: 1
oa_version: Preprint
pmid: 1
publication: The Journal of Chemical Physics
publication_identifier:
eissn:
- 1089-7690
issn:
- 0021-9606
publication_status: published
publisher: American Institute of Physics
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Kinetics of spontaneous filament nucleation via oligomers: Insights from theory
and simulation'
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 145
year: '2016'
...
---
_id: '10378'
abstract:
- lang: eng
text: The ability of biological molecules to replicate themselves is the foundation
of life, requiring a complex cellular machinery. However, a range of aberrant
processes involve the self-replication of pathological protein structures without
any additional assistance. One example is the autocatalytic generation of pathological
protein aggregates, including amyloid fibrils, involved in neurodegenerative disorders.
Here, we use computer simulations to identify the necessary requirements for the
self-replication of fibrillar assemblies of proteins. We establish that a key
physical determinant for this process is the affinity of proteins for the surfaces
of fibrils. We find that self-replication can take place only in a very narrow
regime of inter-protein interactions, implying a high level of sensitivity to
system parameters and experimental conditions. We then compare our theoretical
predictions with kinetic and biosensor measurements of fibrils formed from the
Aβ peptide associated with Alzheimer’s disease. Our results show a quantitative
connection between the kinetics of self-replication and the surface coverage of
fibrils by monomeric proteins. These findings reveal the fundamental physical
requirements for the formation of supra-molecular structures able to replicate
themselves, and shed light on mechanisms in play in the proliferation of protein
aggregates in nature.
acknowledgement: We acknowledge support from the Human Frontier Science Program and
Emmanuel College (A.Š.), the Leverhulme Trust and Magdalene College (A.K.B.), St
John’s College (T.C.T.M.), the Biotechnology and Biological Sciences Research Council
(T.P.J.K. and C.M.D.), the Frances and Augustus Newman Foundation (T.P.J.K.), the
European Research Council (T.P.J.K., T.C.T.M., S.L. and D.F.), and the Engineering
and Physical Sciences Research Council (D.F.).
article_processing_charge: No
article_type: original
author:
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Alexander K.
full_name: Buell, Alexander K.
last_name: Buell
- first_name: Georg
full_name: Meisl, Georg
last_name: Meisl
- first_name: Thomas C. T.
full_name: Michaels, Thomas C. T.
last_name: Michaels
- first_name: Christopher M.
full_name: Dobson, Christopher M.
last_name: Dobson
- first_name: Sara
full_name: Linse, Sara
last_name: Linse
- first_name: Tuomas P. J.
full_name: Knowles, Tuomas P. J.
last_name: Knowles
- first_name: Daan
full_name: Frenkel, Daan
last_name: Frenkel
citation:
ama: Šarić A, Buell AK, Meisl G, et al. Physical determinants of the self-replication
of protein fibrils. Nature Physics. 2016;12(9):874-880. doi:10.1038/nphys3828
apa: Šarić, A., Buell, A. K., Meisl, G., Michaels, T. C. T., Dobson, C. M., Linse,
S., … Frenkel, D. (2016). Physical determinants of the self-replication of protein
fibrils. Nature Physics. Springer Nature. https://doi.org/10.1038/nphys3828
chicago: Šarić, Anđela, Alexander K. Buell, Georg Meisl, Thomas C. T. Michaels,
Christopher M. Dobson, Sara Linse, Tuomas P. J. Knowles, and Daan Frenkel. “Physical
Determinants of the Self-Replication of Protein Fibrils.” Nature Physics.
Springer Nature, 2016. https://doi.org/10.1038/nphys3828.
ieee: A. Šarić et al., “Physical determinants of the self-replication of
protein fibrils,” Nature Physics, vol. 12, no. 9. Springer Nature, pp.
874–880, 2016.
ista: Šarić A, Buell AK, Meisl G, Michaels TCT, Dobson CM, Linse S, Knowles TPJ,
Frenkel D. 2016. Physical determinants of the self-replication of protein fibrils.
Nature Physics. 12(9), 874–880.
mla: Šarić, Anđela, et al. “Physical Determinants of the Self-Replication of Protein
Fibrils.” Nature Physics, vol. 12, no. 9, Springer Nature, 2016, pp. 874–80,
doi:10.1038/nphys3828.
short: A. Šarić, A.K. Buell, G. Meisl, T.C.T. Michaels, C.M. Dobson, S. Linse, T.P.J.
Knowles, D. Frenkel, Nature Physics 12 (2016) 874–880.
date_created: 2021-11-29T10:36:11Z
date_published: 2016-07-18T00:00:00Z
date_updated: 2021-11-29T11:07:25Z
day: '18'
doi: 10.1038/nphys3828
extern: '1'
external_id:
pmid:
- '31031819'
intvolume: ' 12'
issue: '9'
keyword:
- general physics and astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://discovery.ucl.ac.uk/id/eprint/1517406/
month: '07'
oa: 1
oa_version: Preprint
page: 874-880
pmid: 1
publication: Nature Physics
publication_identifier:
eissn:
- 1745-2481
issn:
- 1745-2473
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Physical determinants of the self-replication of protein fibrils
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 12
year: '2016'
...