Department of Molecular Pharmacology and Biological Chemistry, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Curr Top Membr. 2013;71:1-32. doi: 10.1016/B978-0-12-407870-3.00001-9.
In many animal cells, store-operated Ca(2+) release-activated Ca(2+) (CRAC) channels function as an essential route for Ca(2+) entry. CRAC channels control many fundamental cellular functions including gene expression, motility, and cell proliferation, are involved in the etiology of several disease processes including a severe combined immunodeficiency syndrome, and have emerged as major targets for drug development. Although little was known of the molecular mechanisms of CRAC channel operation for several decades, the discovery of Orai1 as a prototypic CRAC channel protein and STIM1 as the endoplasmic reticulum (ER) Ca(2+) sensor has led to rapid progress in our understanding of the mechanisms and functions of CRAC channels. It is now known that activation of CRAC channels following ER Ca(2+) store depletion is governed by several events, which include the redistributions and accumulations of STIM1 and Orai1 into overlapping puncta at peripheral cellular sites, resulting in direct protein-protein interactions between the two proteins. In this chapter, I review the molecular features of the STIM and Orai proteins that regulate the gating and ion conduction mechanisms of CRAC channels.
在许多动物细胞中,储存操纵的钙(Ca(2+))释放激活的钙(Ca(2+))(CRAC)通道作为钙(Ca(2+))进入的基本途径。CRAC 通道控制许多基本的细胞功能,包括基因表达、运动和细胞增殖,涉及几种疾病过程的病因,包括严重联合免疫缺陷综合征,并且已成为药物开发的主要目标。尽管几十年来对 CRAC 通道操作的分子机制知之甚少,但 Orai1 作为典型的 CRAC 通道蛋白和 STIM1 作为内质网(ER)Ca(2+)传感器的发现,使得我们对 CRAC 通道的机制和功能的理解取得了快速进展。现在已知,ER Ca(2+)储存耗尽后 CRAC 通道的激活受几个事件控制,包括 STIM1 和 Orai1 在细胞外周部位重新分布和积累到重叠的小点,导致这两种蛋白质之间的直接蛋白-蛋白相互作用。在本章中,我回顾了调节 CRAC 通道门控和离子传导机制的 STIM 和 Orai 蛋白的分子特征。