Altier Christophe
Department of Physiology and Pharmacology, University of Calgary, 3330 Hospital Drive NW, Calgary, AB, T2N 4N1, Canada,
Subcell Biochem. 2012;63:241-62. doi: 10.1007/978-94-007-4765-4_13.
Voltage-gated ion channels are transmembrane proteins that control nerve impulses and cell homeostasis. Signaling molecules that regulate ion channel activity and density at the plasma membrane must be specifically and efficiently coupled to these channels in order to control critical physiological functions such as action potential propagation. Although their regulation by G-protein receptor activation has been extensively explored, the assembly of ion channels into signaling complexes of GPCRs plays a fundamental role, engaging specific downstream -signaling pathways that trigger precise downstream effectors. Recent work has confirmed that GPCRs can intimately interact with ion channels and serve as -chaperone proteins that finely control their gating and trafficking in subcellular microdomains. This chapter aims to describe examples of GPCR-ion channel co-assembly, focusing mainly on signaling complexes between GPCRs and voltage-gated calcium channels.
电压门控离子通道是控制神经冲动和细胞内稳态的跨膜蛋白。调节质膜上离子通道活性和密度的信号分子必须特异性且高效地与这些通道偶联,以控制诸如动作电位传播等关键生理功能。尽管通过G蛋白偶联受体激活对其调节已得到广泛研究,但离子通道组装到G蛋白偶联受体的信号复合物中起着基本作用,涉及特定的下游信号通路,这些通路触发精确的下游效应器。最近的研究证实,G蛋白偶联受体可与离子通道密切相互作用,并作为伴侣蛋白精细控制其在亚细胞微结构域中的门控和转运。本章旨在描述G蛋白偶联受体 - 离子通道共组装的实例,主要聚焦于G蛋白偶联受体与电压门控钙通道之间的信号复合物。