Interaction between two adapter proteins, PAG and EBP50:: a possible link between membrane rafts and actin cytoskeleton

被引:98
作者
Brdicková, N
Brdicka, T
Andera, L
Spicka, J
Angelisová, P
Milgram, SL
Horejsí, V
机构
[1] Acad Sci Czech Republ, Inst Genet Mol, Prague 14220 4, Czech Republic
[2] Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA
关键词
raft; microdomain; cytoskeleton; adapter protein; PDZ domain;
D O I
10.1016/S0014-5793(01)02955-6
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
Phosphoprotein associated with GEMs (PAG), also known as Csk-binding protein (Cbp), is a broadly expressed palmitoylated transmembrane adapter protein found in membrane rafts, also called GEMs (glycosphingolipid-enriched membrane microdomains). PAG is known to bind and activate the essential regulator of Src-family kinases, cytoplasmic protein tyrosine kinase Csk. In the present study we used the yeast 2-hybrid system to search for additional proteins which might bind to PAG. We have identified the abundant cytoplasmic adapter protein EBP50 (ezrin/radixin/moesin (ERM)-binding phosphoprotein of 50 kDa), also known as NHERF (Na+/H+ exchanger regulatory factor), as a specific PAG-binding partner. The interaction involves the C-terminal sequence (TRL) of PAG and N-terminal PDZ domain(s) of EBP50. As EBP50 is known to interact via its C-terminal domain with the ERM-family proteins, which in turn bind to actin cytoskeleton, the PAG-EBP50 interaction may be important for connecting membrane rafts to the actin cytoskeleton. (C) 2001 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:133 / 136
页数:4
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