The PDZ proteins PICK1, GRIP, and syntenin bind multiple glutamate receptor subtypes - Analysis of PDZ binding motifs

被引:119
作者
Hirbec, H
Perestenko, O
Nishimune, A
Meyer, G
Nakanishi, S
Henley, JM
Dev, KK
机构
[1] Univ Bristol, Sch Med, Dept Anat, MRC,Ctr Synapt Plast, Bristol BS8 1TD, Avon, England
[2] Kyoto Univ, Dept Biol Sci, Fac Med, Kyoto 6068501, Japan
基金
英国医学研究理事会;
关键词
D O I
10.1074/jbc.C200112200
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
Using sequence homology searches, yeast two-hybrid assays and glutathione S-transferase (GST)-pull-down approaches we have identified a series of glutamate receptor subunits that interact differentially with the PDZ proteins GRIP, PICK1, and syntenin. GST-pull-down experiments identified more interactions than detected by yeast two-hybrid assays. We report several receptor-protein interactions, strong ones include: W GRIP and syntenin with mGluR7a, mGluR4a, and mGluR6; (ii) PICK1 and GRIP with mGluR3; and (iii) syntenin with all forms of GluR1-4 and mGluR7b. We further characterized the novel mGluR7a-GRIP interaction found both in yeast two-hybrid and GST-pull-down assays and observed that mGluR7a localization overlapped with GRIP with in hippocampal neurons. The wide range of targets for PICK1, GRIP, and syntenin suggests they may represent a molecular mechanism that can concentrate and/or regulate a number of different receptors at a common site on a synapse. These data also suggest that the structural determinants involved in PDZ interactions are more complex than originally envisaged.
引用
收藏
页码:15221 / 15224
页数:4
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