Evidence map›Paper›PMID 29296664›Full record

ArticleACS central science2017

Long-Range Organization of Membrane-Curving Proteins.

Mijo Simunovic, Anđela Šarić, J Michael Henderson, Ka Yee C Lee, Gregory A Voth

Abstract read
In one paragraph

Article in ACS central science, 2017. 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
–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

23 citing papers in PubMed.

  1. Article
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  7. Bridging Scales: Coarse-Grained Protein Models in Computational Biology.Advances in experimental medicine and biology · 2026
    Review
  8. Article
  9. The Role of Cholesterol in M2 Clustering and Viral Budding Explained.Journal of chemical theory and computation · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
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  20. Article
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

5 authors.

Mijo SimunovicDepartment of Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, United States.
Anđela ŠarićDepartment of Physics and Astronomy, Institute for the Physics of Living Systems, University College London, Gower Street, London, WC1E 6BT, U.K.
J Michael HendersonDepartment of Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, United States.
Ka Yee C LeeDepartment of Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, United States.
Gregory A VothDepartment of Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, United States.

Funding

New Method for Biomembrane SimulationsR01GM063796 · NIGMS · UNIVERSITY OF UTAH · PI VOTH, GREGORY A. · 2001 to 2025
$6.3M
NIGMS NIH HHS R01 GM063796
6 · The paper itself

Abstract

Biological membranes have a central role in mediating the organization of membrane-curving proteins, a dynamic process that has proven to be challenging to probe experimentally. Using atomic force microscopy, we capture the hierarchically organized assemblies of Bin/amphiphysin/Rvs (BAR) proteins on supported lipid membranes. Their structure reveals distinct long linear aggregates of proteins, regularly spaced by up to 300 nm. Employing accurate free-energy calculations from large-scale coarse-grained computer simulations, we found that the membrane mediates the interaction among protein filaments as a combination of short- and long-ranged interactions. The long-ranged component acts at strikingly long distances, giving rise to a variety of micron-sized ordered patterns. This mechanism may contribute to the long-ranged spatiotemporal control of membrane remodeling by proteins in the cell.

Identifiers

PMID29296664
PMCPMC5746856

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.