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磷脂酶Cγ1通过分子间PH结构域控制瞬时受体电位阳离子通道蛋白3的表面表达。

Phospholipase Cgamma1 controls surface expression of TRPC3 through an intermolecular PH domain.

作者信息

van Rossum Damian B, Patterson Randen L, Sharma Sumit, Barrow Roxanne K, Kornberg Michael, Gill Donald L, Snyder Solomon H

机构信息

Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

Nature. 2005 Mar 3;434(7029):99-104. doi: 10.1038/nature03340.

Abstract

Many ion channels are regulated by lipids, but prominent motifs for lipid binding have not been identified in most ion channels. Recently, we reported that phospholipase Cgamma1 (PLC-gamma1) binds to and regulates TRPC3 channels, components of agonist-induced Ca2+ entry into cells. This interaction requires a domain in PLC-gamma1 that includes a partial pleckstrin homology (PH) domain-a consensus lipid-binding and protein-binding sequence. We have developed a gestalt algorithm to detect hitherto 'invisible' PH and PH-like domains, and now report that the partial PH domain of PLC-gamma1 interacts with a complementary partial PH-like domain in TRPC3 to elicit lipid binding and cell-surface expression of TRPC3. Our findings imply a far greater abundance of PH domains than previously appreciated, and suggest that intermolecular PH-like domains represent a widespread signalling mode.

摘要

许多离子通道受脂质调控,但多数离子通道中尚未鉴定出显著的脂质结合基序。最近,我们报道磷脂酶Cγ1(PLC-γ1)与TRPC3通道结合并对其进行调控,TRPC3通道是激动剂诱导Ca2+进入细胞的组分。这种相互作用需要PLC-γ1中的一个结构域,该结构域包含部分普列克底物蛋白同源(PH)结构域——一种公认的脂质结合和蛋白质结合序列。我们开发了一种整体算法来检测迄今“不可见”的PH结构域和类PH结构域,现在报告PLC-γ1的部分PH结构域与TRPC3中互补的部分类PH结构域相互作用,以引发脂质结合和TRPC3的细胞表面表达。我们的发现意味着PH结构域的丰度比之前认为的要高得多,并表明分子间类PH结构域代表一种广泛存在的信号传导模式。

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