N-terminal PDZ domain is required for NHERF dimerization

被引:63
作者
Shenolikar, S
Minkoff, CM
Steplock, DA
Evangelista, C
Liu, MZ
Weinman, EJ
机构
[1] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[2] Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA
[3] Dept Vet Affairs Med Ctr, Med Serv, Baltimore, MD 21201 USA
关键词
Na+/H+ exchanger-3; PSD-95/disc large/ZO-1 domain; protein oligomerization; okadaic acid; protein phosphorylation;
D O I
10.1016/S0014-5793(01)02109-3
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
NHERF, a 55 kDa PDZ-containing protein, binds receptors and ion transporters to mediate signal transduction at the plasma membrane. Recombinant NHERF demonstrated an apparent size of 150 kDa on gel filtration, which could be reduced to approximately 55 kDa by protein denaturing agents, consistent with the formation of NHERF dimers, Biosensor studies established the time- and concentration-dependent dimerization of NHERF. Overlays of recombinant NHERF fragments suggested that NHERF dimerization was principally mediated by the N-terminal PDZ-I domain. In PS120 cells, reversible protein phosphorylation modulated NHERF dimerization and suggested a role for NHERF dimers in hormonal signaling. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:233 / 236
页数:4
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