Identification of a novel Ezrin-binding site in syndecan-2 cytoplasmic domain

被引:51
作者
Granés, F
Berndt, C
Roy, C
Mangeat, P
Reina, M [1 ]
Vilaró, S
机构
[1] Univ Barcelona, Dept Cellular Biol, Fac Biol, Barcelona, Spain
[2] Univ Montpellier 2, Dept Biol Sante, CNRS, URA 1856, Montpellier, France
关键词
syndecan; Ezrin/Radixin/Moesin proteins; protein interaction;
D O I
10.1016/S0014-5793(03)00712-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ERM (Ezrin/Radixin/Moesin) proteins are crosslinkers between plasma membrane proteins and the actin cytoskeleton, thereby involved in the formation of cell adhesion sites. Earlier work showed that Ezrin links syndecan-2 to the actin cytoskeleton. Here we provide evidence that the Ezrin N-terminal domain binds to the syndecan-2 cytoplasmic domain with an estimated K-D of 0.71 muM and without the requirement of other proteins. We also studied the regions in the syndecan-2 cytoplasmic domain implicated in the binding to Ezrin. By truncating the syndecan-2 cytoplasmic domain and by oligopeptide competition assays we show that the Ezrin-binding sequence is not located in the positively charged juxtamembrane region (RMRKK), but in the neighboring sequence DEGSYD. We therefore conclude that the consensus sequence for Ezrin binding is unique among membrane proteins, suggesting a distinct regulation. (C) 2003 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:212 / 216
页数:5
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