Blumer Joe B, Cismowski Mary J, Sato Motohiko, Lanier Stephen M
Department of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.
Trends Pharmacol Sci. 2005 Sep;26(9):470-6. doi: 10.1016/j.tips.2005.07.003.
The identification of AGS proteins as receptor-independent activators of G-protein signaling reveals unexpected mechanisms for the regulation of heterotrimeric G-protein activation and has opened up new areas of research related to the role of G proteins as signal transducers. In addition to their obvious interest associated with G-protein-coupled receptor signaling, AGS proteins might provide alternative binding partners for G-protein subunits that enable them to serve unexpected functions related to cell division, differentiation and organelle structure that might operate independently of a GPCR. Thus, these proteins and the concepts advanced with their discovery highlight the diversity associated with G-protein signaling and present new avenues for the development of therapeutics that target G-protein signaling.
将AGS蛋白鉴定为G蛋白信号的受体非依赖性激活剂,揭示了异源三聚体G蛋白激活调控的意外机制,并开辟了与G蛋白作为信号转导分子作用相关的新研究领域。除了与G蛋白偶联受体信号传导相关的明显研究价值外,AGS蛋白可能为G蛋白亚基提供替代结合伴侣,使它们能够发挥与细胞分裂、分化和细胞器结构相关的意外功能,这些功能可能独立于GPCR发挥作用。因此,这些蛋白质及其发现所提出的概念突出了与G蛋白信号传导相关的多样性,并为开发靶向G蛋白信号传导的治疗方法提供了新途径。