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Multifactorial Regulation of G Protein-Coupled Receptor Endocytosis

机译:G蛋白偶联受体胞吞作用的多因素调节

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摘要

Endocytosis is a process by which cells absorb extracellular materials via the inward budding of vesicles formed from the plasma membrane. Receptor-mediated endocytosis is a highly selective process where receptors with specific binding sites for extracellular molecules internalize via vesicles. G protein-coupled receptors (GPCRs) are the largest single family of plasma-membrane receptors with more than 1000 family members. But the molecular mechanisms involved in the regulation of GPCRs are believed to be highly conserved. For example, receptor phosphorylation in collaboration with β-arrestins plays major roles in desensitization and endocytosis of most GPCRs. Nevertheless, a number of subsequent studies showed that GPCR regulation, such as that by endocytosis, occurs through various pathways with a multitude of cellular components and processes. This review focused on i) functional interactions between homologous and heterologous pathways, ii) methodologies applied for determining receptor endocytosis, iii) experimental tools to determine specific endocytic routes, iv) roles of small guanosine triphosphate-binding proteins in GPCR endocytosis, and v) role of post-translational modification of the receptors in endocytosis.
机译:胞吞作用是细胞通过质膜形成的囊泡向内萌芽吸收细胞外物质的过程。受体介导的内吞作用是高度选择性的过程,其中具有与细胞外分子特异性结合位点的受体通过囊泡内化。 G蛋白偶联受体(GPCR)是最大的单个血浆膜受体家族,有1000多个家族成员。但是据信参与GPCR调节的分子机制是高度保守的。例如,受体磷酸化与β-arrestin协同作用在大多数GPCR的脱敏和胞吞作用中起主要作用。然而,许多后续研究表明,GPCR调控(例如通过内吞作用进行的调控)是通过具有多种细胞成分和过程的各种途径发生的。这篇综述着重于i)同源和异源途径之间的功能相互作用,ii)用于确定受体内吞作用的方法,iii)确定特定内吞途径的实验工具,iv)小鸟苷三磷酸结合蛋白在GPCR内吞作用中的作用,和v)翻译后修饰受体在胞吞作用中的作用。

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