Cargando…

Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web

Tetraspanins regulate cell migration, sperm–egg fusion, and viral infection. Through interactions with one another and other cell surface proteins, tetraspanins form a network of molecular interactions called the tetraspanin web. In this study, we use single-molecule fluorescence microscopy to disse...

Descripción completa

Detalles Bibliográficos
Autores principales: Espenel, Cedric, Margeat, Emmanuel, Dosset, Patrice, Arduise, Cécile, Le Grimellec, Christian, Royer, Catherine A., Boucheix, Claude, Rubinstein, Eric, Milhiet, Pierre-Emmanuel
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518714/
https://www.ncbi.nlm.nih.gov/pubmed/18710926
http://dx.doi.org/10.1083/jcb.200803010
_version_ 1782158600760721408
author Espenel, Cedric
Margeat, Emmanuel
Dosset, Patrice
Arduise, Cécile
Le Grimellec, Christian
Royer, Catherine A.
Boucheix, Claude
Rubinstein, Eric
Milhiet, Pierre-Emmanuel
author_facet Espenel, Cedric
Margeat, Emmanuel
Dosset, Patrice
Arduise, Cécile
Le Grimellec, Christian
Royer, Catherine A.
Boucheix, Claude
Rubinstein, Eric
Milhiet, Pierre-Emmanuel
author_sort Espenel, Cedric
collection PubMed
description Tetraspanins regulate cell migration, sperm–egg fusion, and viral infection. Through interactions with one another and other cell surface proteins, tetraspanins form a network of molecular interactions called the tetraspanin web. In this study, we use single-molecule fluorescence microscopy to dissect dynamics and partitioning of the tetraspanin CD9. We show that lateral mobility of CD9 in the plasma membrane is regulated by at least two modes of interaction that each exhibit specific dynamics. The majority of CD9 molecules display Brownian behavior but can be transiently confined to an interaction platform that is in permanent exchange with the rest of the membrane. These platforms, which are enriched in CD9 and its binding partners, are constant in shape and localization. Two CD9 molecules undergoing Brownian trajectories can also codiffuse, revealing extra platform interactions. CD9 mobility and partitioning are both dependent on its palmitoylation and plasma membrane cholesterol. Our data show the high dynamic of interactions in the tetraspanin web and further indicate that the tetraspanin web is distinct from raft microdomains.
format Text
id pubmed-2518714
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-25187142009-02-25 Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web Espenel, Cedric Margeat, Emmanuel Dosset, Patrice Arduise, Cécile Le Grimellec, Christian Royer, Catherine A. Boucheix, Claude Rubinstein, Eric Milhiet, Pierre-Emmanuel J Cell Biol Research Articles Tetraspanins regulate cell migration, sperm–egg fusion, and viral infection. Through interactions with one another and other cell surface proteins, tetraspanins form a network of molecular interactions called the tetraspanin web. In this study, we use single-molecule fluorescence microscopy to dissect dynamics and partitioning of the tetraspanin CD9. We show that lateral mobility of CD9 in the plasma membrane is regulated by at least two modes of interaction that each exhibit specific dynamics. The majority of CD9 molecules display Brownian behavior but can be transiently confined to an interaction platform that is in permanent exchange with the rest of the membrane. These platforms, which are enriched in CD9 and its binding partners, are constant in shape and localization. Two CD9 molecules undergoing Brownian trajectories can also codiffuse, revealing extra platform interactions. CD9 mobility and partitioning are both dependent on its palmitoylation and plasma membrane cholesterol. Our data show the high dynamic of interactions in the tetraspanin web and further indicate that the tetraspanin web is distinct from raft microdomains. The Rockefeller University Press 2008-08-25 /pmc/articles/PMC2518714/ /pubmed/18710926 http://dx.doi.org/10.1083/jcb.200803010 Text en © 2008 Espenel et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Espenel, Cedric
Margeat, Emmanuel
Dosset, Patrice
Arduise, Cécile
Le Grimellec, Christian
Royer, Catherine A.
Boucheix, Claude
Rubinstein, Eric
Milhiet, Pierre-Emmanuel
Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web
title Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web
title_full Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web
title_fullStr Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web
title_full_unstemmed Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web
title_short Single-molecule analysis of CD9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web
title_sort single-molecule analysis of cd9 dynamics and partitioning reveals multiple modes of interaction in the tetraspanin web
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518714/
https://www.ncbi.nlm.nih.gov/pubmed/18710926
http://dx.doi.org/10.1083/jcb.200803010
work_keys_str_mv AT espenelcedric singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT margeatemmanuel singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT dossetpatrice singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT arduisececile singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT legrimellecchristian singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT royercatherinea singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT boucheixclaude singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT rubinsteineric singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb
AT milhietpierreemmanuel singlemoleculeanalysisofcd9dynamicsandpartitioningrevealsmultiplemodesofinteractioninthetetraspaninweb