Evidence map›Paper›PMID 20727121›Full record

ArticleTraffic (Copenhagen, Denmark)2010

HIV-1 assembly differentially alters dynamics and partitioning of tetraspanins and raft components.

Dimitry N Krementsov, Patrice Rassam, Emmanuel Margeat, Nathan H Roy, Jürgen Schneider-Schaulies, Pierre-Emmanuel Milhiet, Markus Thali

Open access · greenAbstract read
In one paragraph

Article in Traffic (Copenhagen, Denmark), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.3field-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

58 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Methods for Engineering Binders to Multi-Pass Membrane Proteins.Bioengineering (Basel, Switzerland) · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. CD82 and Gangliosides Tune CD81 Membrane Behavior.International journal of molecular sciences · 2021
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Tetraspanin Assemblies in Virus Infection.Frontiers in immunology · 2018
    Review
  18. Article
  19. Article
  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

7 authors at 6 institutions in 3 countries.

Dimitry N KrementsovGraduate Program in Cell and Molecular Biology, University of Vermont, Burlington, VT 05405, USA.
Patrice Rassam
Emmanuel Margeat
Nathan H Roy
Jürgen Schneider-Schaulies
Pierre-Emmanuel Milhiet
Markus Thali
University of Vermont · USCentre de Biologie Structurale · FRInstitute for Neurosciences of Montpellier · FRMARK Resources (United States) · USUniversité de Montpellier · FRUniversity of Würzburg · DE

Funding

VERMONT IMMUNOBIOLOIGY/ INFECTIOUS DISEASES CENTERP20RR021905 · NCRR · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HILL, JACK · 2006 to 2011
$14.5M
Vermont Immunology/Infectious Diseases Training GrantT32AI055402 · NIAID · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI GARY E WARD · 2005 to 2026
$2.7M
Molecular regulation of HIV-1 assembly, release and cell-to-cell transmissionR01AI080302 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI THALI, MARKUS · 2009 to 2013
$1.9M
Spatio-temporal analysis of HIV-1 assembly and releaseR56AI047727 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI THALI, MARKUS · 2008 to 2008
$376k
NCRR NIH HHS P20 RR021905NIAID NIH HHS R01 AI 080302NIAID NIH HHS R01 AI080302NIAID NIH HHS R56 AI047727NIAID NIH HHS T32 AI055402PHS HHS R01 A1072021-0251
6 · The paper itself

Abstract

Partitioning of membrane proteins into various types of microdomains is crucial for many cellular functions. Tetraspanin-enriched microdomains (TEMs) are a unique type of protein-based microdomain, clearly distinct from membrane rafts, and important for several cellular processes such as fusion, migration and signaling. Paradoxically, HIV-1 assembly/egress occurs at TEMs, yet the viral particles also incorporate raft lipids. Using different quantitative microscopy approaches, we investigated the dynamic relationship between TEMs, membrane rafts and HIV-1 exit sites, focusing mainly on the tetraspanin CD9. Our results show that clustering of CD9 correlates with multimerization of the major viral structural component, Gag, at the plasma membrane. CD9 exhibited confined behavior and reduced lateral mobility at viral assembly sites, suggesting that Gag locally traps tetraspanins. In contrast, the raft lipid GM1 and the raft-associated protein CD55, while also recruited to assembly/budding sites, were only transiently trapped in these membrane areas. CD9 recruitment and confinement were found to be partially dependent on cholesterol, while those of CD55 were completely dependent on cholesterol. Importantly, our findings support the emerging concept that cellular and viral components, instead of clustering at preexisting microdomain platforms, direct the formation of distinct domains for the execution of specific functions.

Indexed as

AnimalsChlorocebus aethiopsFluorescence Recovery After PhotobleachingHeLa CellsHIV-1HumansMembrane GlycoproteinsMembrane MicrodomainsVero CellsVirus AssemblyMembrane Glycoproteins

Identifiers

PMID20727121
PMCPMC4073295
OpenAlexW2155957331

What OpenQuestion holds

Textmetadata
LicenceTDM
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.