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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...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2008
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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 |
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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 |
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