Evidence map›Paper›PMID 31913664›Full record

ReviewAnnual review of biophysics2020

Principles and Applications of Biological Membrane Organization.

Wade F Zeno, Kasey J Day, Vernita D Gordon, Jeanne C Stachowiak

Abstract readReview
In one paragraph

Review in Annual review of biophysics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Biophysical modeling of membrane curvature generation and curvature sensing by the glycocalyx.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Unraveling membrane properties at the organelle-level with LipidDyn.Computational and structural biotechnology journal · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. Amphiphilic proteins coassemble into multiphasic condensates and act as biomolecular surfactants.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Article
  18. DNA-Mediated Stack Formation of Nanodiscs.Molecules (Basel, Switzerland) · 2021
    Article
  19. Clathrin senses membrane curvature.Biophysical journal · 2021
    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

4 authors.

Wade F ZenoDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, USA; email: jcstach@austin.utexas.edu.
Kasey J DayDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, USA; email: jcstach@austin.utexas.edu.
Vernita D GordonDepartment of Physics, The University of Texas at Austin, Austin, Texas 78712, USA.
Jeanne C StachowiakDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78712, USA; email: jcstach@austin.utexas.edu.

Funding

Assessing the roles of biofilm structure and mechanics in pathogenic, persistent infectionsR01AI121500 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI GORDON, VERNITA DIANE · 2017 to 2020
$1.5M
Intrinsically disordered proteins as physical drivers of membrane trafficR01GM120549 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI STACHOWIAK, JEANNE CASSTEVENS · 2017 to 2020
$1.4M
Protein Droplets as Catalysts of Coated Vesicle AssemblyF32GM133138 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI DAY, KASEY JILL · 2019 to 2021
$144k
Intrinsically Disordered Proteins as Sensors of Membrane CurvatureF32GM128316 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI ZENO, WADE F · 2018 to 2019
$120k
NIAID NIH HHS R01 AI121500NIGMS NIH HHS F32 GM128316NIGMS NIH HHS F32 GM133138NIGMS NIH HHS R01 GM120549
6 · The paper itself

Abstract

Many critical biological events, including biochemical signaling, membrane traffic, and cell motility, originate at membrane surfaces. Each such event requires that members of a specific group of proteins and lipids rapidly assemble together at a specific site on the membrane surface. Understanding the biophysical mechanisms that stabilize these assemblies is critical to decoding and controlling cellular functions. In this article, we review progress toward a quantitative biophysical understanding of the mechanisms that drive membrane heterogeneity and organization. We begin from a physical perspective, reviewing the fundamental principles and key experimental evidence behind each proposed mechanism. We then shift to a biological perspective, presenting key examples of the role of heterogeneity in biology and asking which physical mechanisms may be responsible. We close with an applied perspective, noting that membrane heterogeneity provides a novel therapeutic target that is being exploited by a growing number of studies at the interface of biology, physics, and engineering.

Indexed as

Biophysical PhenomenaCell MembraneHumansSignal Transductionbiological membranelipid biophysicsmembrane heterogeneitymembrane organizationphase separation

Identifiers

PMID31913664
PMCPMC7299165

What OpenQuestion holds

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Registered trials

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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.