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

被引:114
作者
Espenel, Cedric [1 ,2 ]
Margeat, Emmanuel [1 ,2 ]
Dosset, Patrice [1 ,2 ]
Arduise, Cecile [3 ,4 ]
Le Grimellec, Christian [1 ,2 ]
Royer, Catherine A. [1 ,2 ]
Boucheix, Claude [3 ,4 ]
Rubinstein, Eric [3 ,4 ]
Milhiet, Pierre-Emmanuel [1 ,2 ]
机构
[1] INSERM, U554, F-34090 Montpellier, France
[2] Univ Montpellier, CNRS, Unite Mixte Rech 5048, Ctr Biochim Struct, F-34090 Montpellier, France
[3] INSERM, U602, F-94804 Villejuif, France
[4] Univ Paris 11, Inst Andre Lwoff, F-94801 Villejuif, France
关键词
D O I
10.1083/jcb.200803010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:765 / 776
页数:12
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