Evidence map›Paper›PMID 23931319›Full record

ArticleBiophysical journal2013

Protein-mediated transformation of lipid vesicles into tubular networks.

Mijo Simunovic, Carsten Mim, Thomas C Marlovits, Guenter Resch, Vinzenz M Unger, Gregory A Voth

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 86 citations in OpenAlex.

  1. Bridging Scales: Coarse-Grained Protein Models in Computational Biology.Advances in experimental medicine and biology · 2026
    Review
  2. Review
  3. Prediction and Evaluation of Protein Aggregation with Computational Methods.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  4. Article
  5. Changing Your Martini Can Still Give You a Hangover.Journal of chemical theory and computation · 2024
    Article
  6. Lipid Organization by the Caveolin-1 Complex.bioRxiv : the preprint server for biology · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Membrane signalosome: where biophysics meets systems biology.Current opinion in systems biology · 2021
    Article
  14. Article
  15. The plasma membrane as a mechanochemical transducer.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Simulations of N-BAR Protein Interactions with Membranes.Journal of physics D: Applied physics · 2018
    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

6 authors at 3 institutions in 2 countries.

Mijo SimunovicDepartment of Chemistry, Institute for Biophysical Dynamics, The University of Chicago, Illinois, USA.
Carsten Mim
Thomas C Marlovits
Guenter Resch
Vinzenz M Unger
Gregory A Voth
Chicago Institute for Psychoanalysis · USInstitute of Molecular Biotechnology · ATNorthwestern University · US

Funding

New Method for Biomembrane SimulationsR01GM063796 · NIGMS · UNIVERSITY OF UTAH · PI VOTH, GREGORY A. · 2001 to 2025
$6.3M
Structural Biology of Membrane ScaffoldsR01GM094479 · NIGMS · NORTHWESTERN UNIVERSITY · PI UNGER, VINZENZ · 2010 to 2013
$1.6M
NIGMS NIH HHS GM063796NIGMS NIH HHS GM094479NIGMS NIH HHS R01 GM063796NIGMS NIH HHS R01 GM094479
6 · The paper itself

Abstract

Key cellular processes are frequently accompanied by protein-facilitated shape changes in the plasma membrane. N-BAR-domain protein modules generate curvature by means of complex interactions with the membrane surface. The way they assemble and the mechanism by which they operate are largely dependent on their binding density. Although the mechanism at lower densities has recently begun to emerge, how membrane scaffolds form at high densities remains unclear. By combining electron microscopy and multiscale simulations, we show that N-BAR proteins at high densities can transform a lipid vesicle into a 3D tubular network. We show that this process is a consequence of excess adhesive energy combined with the local stiffening of the membrane, which occurs in a narrow range of mechanical properties of both the membrane and the protein. We show that lipid diffusion is significantly reduced by protein binding at this density regime and even more in areas of high Gaussian curvature, indicating a potential effect on molecular transport in cells. Finally, we reveal that the breaking of the bilayer topology is accompanied by the nematic arrangement of the protein on the surface, a structural motif that likely drives the formation of reticular structures in living cells.

Indexed as

Amino Acid SequenceDiffusionLipid BilayersLiposomesMembrane ProteinsMolecular Dynamics SimulationMolecular Sequence DataProtein BindingProtein Structure, TertiaryLipid BilayersLiposomesMembrane Proteins

Identifiers

PMID23931319
PMCPMC3736692
OpenAlexW2020315971

What OpenQuestion holds

Textmetadata
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.