Evidence map›Paper›PMID 28648660›Full record

ArticleCell2017

Friction Mediates Scission of Tubular Membranes Scaffolded by BAR Proteins.

Mijo Simunovic, Jean-Baptiste Manneville, Henri-François Renard, Emma Evergren, Krishnan Raghunathan, Dhiraj Bhatia, Anne K Kenworthy, Gregory A Voth, Jacques Prost, Harvey T McMahon and 3 more

Abstract read
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
–field-weighted citation impact
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

116 citing papers in PubMed.

  1. Article
  2. Devising a divisome for synthetic cells.Nature reviews. Chemistry · 2026
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  7. Review
  8. Article
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  11. Spatial N-glycan rearrangement on αNature communications · 2025
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Nanoscale dynamics of Dynamin 1 helices reveals squeeze-twist deformation mode critical for membrane fission.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  19. Article
  20. Article

56 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Mijo SimunovicLaboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005 Paris, France; Sorbonne Universités, UPMC University Paris 06, 75005 Paris, France; Department of Chemistry, Institute for Biophysical Dynamics, James Franck Institute, The University of Chicago, 5735 S. Ellis Avenue, Chicago, IL 60637, USA.
Jean-Baptiste MannevilleSubcellular Structure and Cellular Dynamics Unit, Institut Curie, PSL Research University, CNRS UMR144, 75005 Paris, France.
Henri-François RenardChemical Biology of Membranes and Therapeutic Delivery Unit, Institut Curie, PSL Research University, CNRS UMR3666, INSERM U1143, 75005 Paris, France.
Emma EvergrenMedical Research Council Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK; Centre for Cancer Research and Cell Biology, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.
Krishnan RaghunathanDepartment of Molecular Physiology and Biophysics, Vanderbilt School of Medicine, 718 Light Hall, Nashville, TN 37232, USA.
Dhiraj BhatiaChemical Biology of Membranes and Therapeutic Delivery Unit, Institut Curie, PSL Research University, CNRS UMR3666, INSERM U1143, 75005 Paris, France.
Anne K KenworthyDepartment of Molecular Physiology and Biophysics, Vanderbilt School of Medicine, 718 Light Hall, Nashville, TN 37232, USA.
Gregory A VothDepartment of Chemistry, Institute for Biophysical Dynamics, James Franck Institute, The University of Chicago, 5735 S. Ellis Avenue, Chicago, IL 60637, USA.
Jacques ProstLaboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005 Paris, France; Sorbonne Universités, UPMC University Paris 06, 75005 Paris, France; Mechanobiology Institute, National University of Singapore, Singapore 119077, Singapore.
Harvey T McMahonMedical Research Council Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK.
Ludger JohannesChemical Biology of Membranes and Therapeutic Delivery Unit, Institut Curie, PSL Research University, CNRS UMR3666, INSERM U1143, 75005 Paris, France.
Patricia BassereauLaboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005 Paris, France; Sorbonne Universités, UPMC University Paris 06, 75005 Paris, France. Electronic address: patricia.bassereau@curie.fr.
Andrew Callan-JonesLaboratoire Matière et Systèmes Complexes, CNRS UMR7057, 75205 Paris, France. Electronic address: andrew.callan-jones@univ-paris-diderot.fr.

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
New Method for Biomembrane SimulationsR01GM063796 · NIGMS · UNIVERSITY OF UTAH · PI VOTH, GREGORY A. · 2001 to 2025
$6.3M
Function and assembly of toxin-stabilized domainsR01GM106720 · NIGMS · VANDERBILT UNIVERSITY · PI KENWORTHY, ANNE K · 2013 to 2020
$2.7M
European Research Council 340485Medical Research Council MC_U105178795NIDDK NIH HHS P30 DK058404NIGMS NIH HHS R01 GM063796NIGMS NIH HHS R01 GM106720
6 · The paper itself

Abstract

Membrane scission is essential for intracellular trafficking. While BAR domain proteins such as endophilin have been reported in dynamin-independent scission of tubular membrane necks, the cutting mechanism has yet to be deciphered. Here, we combine a theoretical model, in vitro, and in vivo experiments revealing how protein scaffolds may cut tubular membranes. We demonstrate that the protein scaffold bound to the underlying tube creates a frictional barrier for lipid diffusion; tube elongation thus builds local membrane tension until the membrane undergoes scission through lysis. We call this mechanism friction-driven scission (FDS). In cells, motors pull tubes, particularly during endocytosis. Through reconstitution, we show that motors not only can pull out and extend protein-scaffolded tubes but also can cut them by FDS. FDS is generic, operating even in the absence of amphipathic helices in the BAR domain, and could in principle apply to any high-friction protein and membrane assembly.

Indexed as

EndocytosisAcyltransferasesAnimalsBiomechanical PhenomenaFrictionHumansLipid MetabolismMembrane ProteinsProtein DomainsRats2-acylglycerophosphate acyltransferaseACAP2 protein, humanAcyltransferasesMembrane ProteinsBAR domaindiffusion barrierendocytosisendophilinfriction-driven scissionin vitro reconstitutionmembrane scissionmembrane tubemolecular motorsscaffold

Identifiers

PMID28648660
PMCPMC5576516

What OpenQuestion holds

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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.