4.5 Article

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

期刊

FEBS LETTERS
卷 507, 期 2, 页码 133-136

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/S0014-5793(01)02955-6

关键词

raft; microdomain; cytoskeleton; adapter protein; PDZ domain

资金

  1. NHLBI NIH HHS [HL63755] Funding Source: Medline

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据