Andreeva Alexandra V, Kutuzov Mikhail A, Voyno-Yasenetskaya Tatyana A
Department of Pharmacology, College of Medicine, University of Illinois at Chicago, 909 S, Wolcott Ave, Chicago, Illinois 60612, USA.
J Mol Signal. 2007 Oct 30;2:13. doi: 10.1186/1750-2187-2-13.
Heterotrimeric G proteins are ubiquitous signaling partners of seven transmembrane-domain G-protein-coupled receptors (GPCRs), the largest (and most important pharmacologically) receptor family in mammals. A number of scaffolding proteins have been identified that regulate various facets of GPCR signaling. In this review, we summarize current knowledge concerning those scaffolding proteins that are known to directly bind heterotrimeric G proteins, and discuss the composition of the protein complexes they assemble and their effects on signal transduction. Emerging evidence about possible ways of regulation of activity of these scaffolding proteins is also discussed.
异源三聚体G蛋白是七跨膜结构域G蛋白偶联受体(GPCRs)普遍存在的信号转导伙伴,GPCRs是哺乳动物中最大(且在药理学上最重要)的受体家族。已鉴定出多种支架蛋白,它们调节GPCR信号转导的各个方面。在本综述中,我们总结了目前关于那些已知直接结合异源三聚体G蛋白的支架蛋白的知识,并讨论了它们组装的蛋白质复合物的组成及其对信号转导的影响。还讨论了关于这些支架蛋白活性可能调节方式的新证据。