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Cellular mechanisms that determine selective RGS protein regulation of G protein-coupled receptor signaling

机译:确定G蛋白偶联受体信号传导的选择性RGS蛋白调控的细胞机制

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摘要

Regulators of G protein signaling (RGS proteins) bind directly to activated G alpha subunits to inhibit their signaling. However, recent findings show that RGS proteins selectively regulate signaling by certain G protein-coupled receptors (GPCRs) in cells, irrespective of the coupled G protein. New studies support an emerging model that suggests RGS proteins utilize both direct and indirect mechanisms to form stable functional pairs with preferred GPCRs to selectively modulate the signaling functions of those receptors and linked G proteins. Here, we discuss these findings and their implications for established models of GPCR signaling. (c) 2006 Elsevier Ltd. All rights reserved.
机译:G蛋白信号的调节剂(RGS蛋白)直接与活化的G alpha亚基结合,以抑制其信号传导。但是,最近的发现表明,RGS蛋白选择性地调节细胞中某些G蛋白偶联受体(GPCR)的信号传导,而与偶联的G蛋白无关。新研究支持一种新兴模型,该模型表明RGS蛋白利用直接和间接机制与首选GPCR形成稳定的功能对,从而选择性地调节那些受体和连接的G蛋白的信号传导功能。在这里,我们讨论这些发现及其对GPCR信号传导建立模型的影响。 (c)2006 Elsevier Ltd.保留所有权利。

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