Extensive temporally regulated reorganization of the lipid raft proteome following T-cell antigen receptor triggering

被引:122
作者
Bini, L
Pacini, S
Liberatori, S
Valensin, S
Pellegrini, M
Raggiaschi, R
Pallini, V
Baldari, CT
机构
[1] Univ Siena, Dept Evolutionary Biol, I-53100 Siena, Italy
[2] Univ Siena, Dept Mol Biol, I-53100 Siena, Italy
关键词
membrane microdomain; protein segregation; proteomics; signal transduction; T-lymphocyte;
D O I
10.1042/BJ20020503
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Signalling by immunoreceptors is orchestrated at specific plasma membrane microdomains, referred to as lipid rafts. Here we present a proteomics approach to the temporal analysis of protein association with lipid rafts following T-cell antigen receptor (TCR) triggering. We show that TCR engagement promotes the temporally regulated recruitment of proteins participating in the TCR signalling cascade to lipid rafts. Furthermore, TCR triggering results in profound modifications in the composition of lipid rafts involving a number of proteins associated either directly or indirectly with both plasma and intracellular membranes. Raft-associated proteins can be clustered according to their temporal profile of raft association. The data identify lipid rafts as highly dynamic structures and reveal a dramatic impact of surface TCR triggering not only on components of the TCR signalling machinery but also on proteins implicated in a number of diverse cellular processes.
引用
收藏
页码:301 / 309
页数:9
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