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支架蛋白在TRPC依赖性钙内流调节中的作用。

Role of Scaffolding Proteins in the Regulation of TRPC-Dependent Calcium Entry.

作者信息

Constantin Bruno

机构信息

Laboratory STIM, ERL-7368 CNRS-Université de Poitiers, 1, rue Georges Bonnet, Bat. B36, Pôle Biologie-Santé, 86000, Poitiers, France.

出版信息

Adv Exp Med Biol. 2016;898:379-403. doi: 10.1007/978-3-319-26974-0_16.

DOI:10.1007/978-3-319-26974-0_16
PMID:27161237
Abstract

Plasma membrane ion channels, and in particular TRPC channels need a specific membrane environment and association with scaffolding, signaling, and cytoskeleton proteins in order to play their important functional role. The molecular composition of TRPC channels is an important factor in determining channel activation mechanisms. TRPC proteins are incorporated in macromolecular complexes including several key Ca(2 +) signaling proteins as well as proteins involved in vesicle trafficking, cytoskeletal interactions, and scaffolding. Evidence has been provided for association of TRPC with calmodulin (CaM), IP3R, PMCA, Gq/11, RhoA, and a variety of scaffolding proteins. The interaction between TRPC channels with adaptor proteins, determines their mode of regulation as well as their cellular localization and function. Adaptor proteins do not display any enzymatic activity but act as scaffold for the building of signaling complexes. The scaffolding proteins are involved in the assembling of these Ca(2+) signaling complexes, the correct sub-cellular localization of protein partners, and the regulation of the TRPC channelosome. In particular, these proteins, via their multiple protein-protein interaction motifs, can interact with various ion channels involved in the transmembrane potential, and membrane excitability. Scaffolding proteins are key components for the functional organization of TRPC channelosomes that serves as a platform regulating slow Ca(2+) entry, spatially and temporally controlled [Ca(2+)]i signals and Ca(2+) -dependent cellular functions.

摘要

质膜离子通道,尤其是瞬时受体电位经典型(TRPC)通道,需要特定的膜环境并与支架蛋白、信号蛋白和细胞骨架蛋白相互作用,才能发挥其重要的功能作用。TRPC通道的分子组成是决定通道激活机制的重要因素。TRPC蛋白整合在大分子复合物中,这些复合物包括几种关键的Ca(2+)信号蛋白以及参与囊泡运输、细胞骨架相互作用和支架构建的蛋白。已有证据表明TRPC与钙调蛋白(CaM)、肌醇三磷酸受体(IP3R)、质膜钙泵(PMCA)、Gq/11、RhoA以及多种支架蛋白有关联。TRPC通道与衔接蛋白之间的相互作用决定了它们的调节方式以及细胞定位和功能。衔接蛋白不显示任何酶活性,但作为构建信号复合物的支架发挥作用。支架蛋白参与这些Ca(2+)信号复合物的组装、蛋白伴侣在亚细胞水平的正确定位以及TRPC通道体的调节。特别是,这些蛋白通过其多个蛋白质 - 蛋白质相互作用基序,可以与参与跨膜电位和膜兴奋性的各种离子通道相互作用。支架蛋白是TRPC通道体功能组织的关键组成部分,TRPC通道体作为一个平台,在空间和时间上控制慢Ca(2+)内流、[Ca(2+)]i信号以及Ca(2+)依赖性细胞功能。

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