Evidence map›Paper›PMID 35867835›Full record

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

Active emulsions in living cell membranes driven by contractile stresses and transbilayer coupling.

Suvrajit Saha, Amit Das, Chandrima Patra, Anupama Ambika Anilkumar, Parijat Sil, Satyajit Mayor, Madan Rao

Open access · greenAbstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  7. Cell-intrinsic mechanical regulation of plasma membrane accumulation at the cytokinetic furrow.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Review
  10. Cell type-specific regulation of CFTR trafficking-on the verge of progress.Frontiers in cell and developmental biology · 2024
    Review
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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

7 authors at 1 institution in 2 countries.

Suvrajit SahaCellular Organization and Signalling, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India.ORCID 0000-0001-6631-0464
Amit DasCellular Organization and Signalling, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India.
Chandrima PatraCellular Organization and Signalling, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India.
Anupama Ambika AnilkumarCellular Organization and Signalling, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India.
Parijat SilCellular Organization and Signalling, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India.
Satyajit MayorCellular Organization and Signalling, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India.ORCID 0000-0001-9842-6963
Madan RaoCellular Organization and Signalling, National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India.
Tata Institute of Fundamental Research · IN

Funding

Wellcome Trust
6 · The paper itself

Abstract

The spatiotemporal organization of proteins and lipids on the cell surface has direct functional consequences for signaling, sorting, and endocytosis. Earlier studies have shown that multiple types of membrane proteins, including transmembrane proteins that have cytoplasmic actin binding capacity and lipid-tethered glycosylphosphatidylinositol-anchored proteins (GPI-APs), form nanoscale clusters driven by active contractile flows generated by the actin cortex. To gain insight into the role of lipids in organizing membrane domains in living cells, we study the molecular interactions that promote the actively generated nanoclusters of GPI-APs and transmembrane proteins. This motivates a theoretical description, wherein a combination of active contractile stresses and transbilayer coupling drives the creation of active emulsions, mesoscale liquid order (lo) domains of the GPI-APs and lipids, at temperatures greater than equilibrium lipid phase segregation. To test these ideas, we use spatial imaging of molecular clustering combined with local membrane order, and we demonstrate that mesoscopic domains enriched in nanoclusters of GPI-APs are maintained by cortical actin activity and transbilayer interactions and exhibit significant lipid order, consistent with predictions of the active composite model.

Indexed as

ActinsActomyosinCell MembraneGPI-Linked ProteinsStress, MechanicalAnimalsCHO CellsCricetulusLipidsActinsActomyosinGPI-Linked ProteinsLipidsactive mechanicsmembrane orderingmesoscalenanoscaleplasma membrane

Identifiers

PMID35867835
PMCPMC9335261
OpenAlexW4286586568

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.