Evidence map›Paper›PMID 9876143›Full record

ArticleBiophysical journal1999

Weak dependence of mobility of membrane protein aggregates on aggregate size supports a viscous model of retardation of diffusion.

D F Kucik, E L Elson, M P Sheetz

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Impaired Glycine Receptor Trafficking in Neurological Diseases.Frontiers in molecular neuroscience · 2018
    Review
  10. Protein Crowding within the Postsynaptic Density Can Impede the Escape of Membrane Proteins.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  11. Article
  12. There Is No Simple Model of the Plasma Membrane Organization.Frontiers in cell and developmental biology · 2016
    Review
  13. Wanted: scalable tracers for diffusion measurements.The journal of physical chemistry. B · 2014
    Review
  14. Review
  15. Article
  16. Article
  17. Dynamics of a polymer chain confined in a membrane.The European physical journal. E, Soft matter · 2011
    Article
  18. Article
  19. A molecular clutch between the actin flow and N-cadherin adhesions drives growth cone migration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008
    Article
  20. Lateral mobility of proteins in liquid membranes revisited.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

D F KucikBirmingham Veterans Affairs Medical Center, Birmingham, AL and Department of Pathology, University of Alabama, Birmingham 35294, USA. kucik@path.uab.edu
E L Elson
M P Sheetz
Duke University · USUniversity of Alabama at Birmingham · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteins in plasma membranes diffuse more slowly than proteins inserted into artificial lipid bilayers. On a long-range scale (>250 nm), submembrane barriers, or skeleton fences that hinder long-range diffusion and create confinement zones, have been described. Even within such confinement zones, however, diffusion of proteins is much slower than predicted by the viscosity of the lipid. The cause of this slowing of diffusion on the micro scale has not been determined and is the focus of this paper. One way to approach this question is to determine the dependence of particle motion on particle size. Some current models predict that the diffusion coefficient of a membrane protein aggregate will depend strongly on its size, while others do not. We have measured the diffusion coefficients of membrane glycoprotein aggregates linked together by concanavalin A molecules bound to beads of various sizes, and also the diffusion coefficients of individual concanavalin A binding proteins. The measurements demonstrate at most a weak dependence of diffusion coefficient on aggregate size. This finding supports retardation by viscous effects, and is not consistent with models involving direct interaction of diffusing proteins with cytoskeletal elements.

Indexed as

AnimalsBiophysical PhenomenaBiophysicsCell MembraneCells, CulturedDiffusionGoldfishIn Vitro TechniquesMacromolecular SubstancesMembrane GlycoproteinsMicroscopy, ElectronModels, BiologicalProtein BindingViscosityMacromolecular SubstancesMembrane Glycoproteins

Identifiers

PMID9876143
PMCPMC1302520
OpenAlexW2030752639

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.