van Rossum Damian B, Patterson Randen L, Sharma Sumit, Barrow Roxanne K, Kornberg Michael, Gill Donald L, Snyder Solomon H
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Nature. 2005 Mar 3;434(7029):99-104. doi: 10.1038/nature03340.
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.
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。