Importance of the G protein γ subunit in activating G protein-coupled inward rectifier K+ channels

被引:16
作者
Kawano, T
Chen, L
Watanabe, SY
Yamauchi, J
Kaziro, Y
Nakajima, Y
Nakajima, S
Itoh, H
机构
[1] Tokyo Inst Technol, Fac Biosci & Biotechnol, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Univ Illinois, Dept Anat & Cell Biol, Chicago, IL 60612 USA
[3] Univ Illinois, Dept Pharmacol, Chicago, IL 60612 USA
关键词
G protein-coupled inward rectifier K+ channel; G protein; G beta gamma; electrophysiology; immunoprecipitation; HEK; 293; cell;
D O I
10.1016/S0014-5793(99)01656-7
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
The G protein-coupled inward rectifier K+ channel (GIRK) is activated by direct interaction with the heterotrimeric GTP-binding protein beta gamma subunits (G beta gamma), However, the precise role of G beta and G gamma in GIRK activation remains to be elucidated. Using transient expression of GIRK1, GIRK2, G beta 1, and G gamma 2 in human embryonic kidney 293 cells, we show that C-terminal mutants of G beta 1, which do not bind to G gamma 2, are still able to associate with GIRK, but these mutants are unable to induce activation of GIRK channels. In contrast, other C-terminal mutants of G beta 1 that bind to G gamma 2, are capable of activating the GIRK channel. These results suggest that G gamma plays a more important role than that of an anchoring device for the G beta gamma-induced GIRK activation. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:355 / 359
页数:5
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