Evidence map›Paper›PMID 34983838›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Physical mechanisms of ESCRT-III-driven cell division.

Lena Harker-Kirschneck, Anne E Hafner, Tina Yao, Christian Vanhille-Campos, Xiuyun Jiang, Andre Pulschen, Fredrik Hurtig, Dawid Hryniuk, Siân Culley, Ricardo Henriques and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Membrane bending energy selects for compact growth of protein assemblies.bioRxiv : the preprint server for biology · 2025
    Article
  5. Review
  6. A self-assembling surface layer flattens the cytokinetic furrow to aid cell division in an archaeon.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Review
  8. Article
  9. Characterization of extracellular vesicles released fromPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  10. Making the cut: Multiscale simulation of membrane remodeling.Current opinion in structural biology · 2024
    Review
  11. Making the cut: Multiscale simulation of membrane remodeling.Current opinion in structural biology · 2024
    Review
  12. Review
  13. Vps60 initiates alternative ESCRT-III filaments.The Journal of cell biology · 2023
    Article
  14. Article
  15. Review
  16. Morphological transformations of vesicles with confined flexible filaments.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  18. Molecular mechanism of GTP binding- and dimerization-induced enhancement of Sar1-mediated membrane remodeling.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Modeling membrane reshaping driven by dynamic protein assemblies.Current opinion in structural biology · 2023
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Lena Harker-KirschneckDepartment of Physics & Astronomy, University College London, London WC1E 6BT, United Kingdom.ORCID 0000-0001-6092-6591
Anne E HafnerDepartment of Physics & Astronomy, University College London, London WC1E 6BT, United Kingdom.
Tina YaoDepartment of Physics & Astronomy, University College London, London WC1E 6BT, United Kingdom.ORCID 0000-0003-0470-311X
Christian Vanhille-CamposDepartment of Physics & Astronomy, University College London, London WC1E 6BT, United Kingdom.
Xiuyun JiangDepartment of Physics & Astronomy, University College London, London WC1E 6BT, United Kingdom.ORCID 0000-0001-6884-411X
Andre PulschenMedical Research Council Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, United Kingdom.
Fredrik HurtigMedical Research Council Laboratory of Molecular Biology, University of Cambridge, Cambridge CB2 0QH, United Kingdom.ORCID 0000-0003-2461-0877
Dawid HryniukDepartment of Physics & Astronomy, University College London, London WC1E 6BT, United Kingdom.
Siân CulleyInstitute for the Physics of Living Systems, University College London, London WC1E 6BT, United Kingdom.
Ricardo HenriquesInstitute for the Physics of Living Systems, University College London, London WC1E 6BT, United Kingdom.ORCID 0000-0002-2043-5234
Buzz BaumInstitute for the Physics of Living Systems, University College London, London WC1E 6BT, United Kingdom.
Anđela ŠarićDepartment of Physics & Astronomy, University College London, London WC1E 6BT, United Kingdom; a.saric@ucl.ac.uk.ORCID 0000-0002-7854-2139
MRC Laboratory for Molecular Cell Biology · GBMRC Laboratory of Molecular Biology · GBUniversity College London · GB

Funding

Medical Research Council MC_UP_1201/27Wellcome TrustWellcome Trust 203276/Z/16/Z
6 · The paper itself

Abstract

Living systems propagate by undergoing rounds of cell growth and division. Cell division is at heart a physical process that requires mechanical forces, usually exerted by assemblies of cytoskeletal polymers. Here we developed a physical model for the ESCRT-III-mediated division of archaeal cells, which despite their structural simplicity share machinery and evolutionary origins with eukaryotes. By comparing the dynamics of simulations with data collected from live cell imaging experiments, we propose that this branch of life uses a previously unidentified division mechanism. Active changes in the curvature of elastic cytoskeletal filaments can lead to filament perversions and supercoiling, to drive ring constriction and deform the overlying membrane. Abscission is then completed following filament disassembly. The model was also used to explore how different adenosine triphosphate (ATP)-driven processes that govern the way the structure of the filament is changed likely impact the robustness and symmetry of the resulting division. Comparisons between midcell constriction dynamics in simulations and experiments reveal a good agreement with the process when changes in curvature are implemented at random positions along the filament, supporting this as a possible mechanism of ESCRT-III-dependent division in this system. Beyond archaea, this study pinpoints a general mechanism of cytokinesis based on dynamic coupling between a coiling filament and the membrane.

Indexed as

Adenosine TriphosphateArchaeaCell DivisionCell MembraneCytokinesisCytoskeletonEndosomal Sorting Complexes Required for TransportSulfolobus acidocaldariusAdenosine TriphosphateEndosomal Sorting Complexes Required for Transportarchaeacell divisionESCRT-IIImembrane simulationssoft matter

Identifiers

PMID34983838
PMCPMC8740586
OpenAlexW4205608832

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.