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新 RAMPage 的黎明。

Dawn of a New RAMPage.

机构信息

Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Trends Pharmacol Sci. 2020 Apr;41(4):249-265. doi: 10.1016/j.tips.2020.01.009. Epub 2020 Feb 27.

Abstract

Receptor activity-modifying proteins (RAMPs) interact with G-protein-coupled receptors (GPCRs) to modify their functions, imparting significant implications upon their physiological and therapeutic potentials. Resurging interest in identifying RAMP-GPCR interactions has recently been fueled by coevolution studies and orthogonal technological screening platforms. These new studies reveal previously unrecognized RAMP-interacting GPCRs, many of which expand beyond Class B GPCRs. The consequences of these interactions on GPCR function and physiology lays the foundation for new molecular therapeutic targets, as evidenced by the recent success of erenumab. Here, we highlight recent papers that uncovered novel RAMP-GPCR interactions, human RAMP-GPCR disease-causing mutations, and RAMP-related human pathologies, paving the way for a new era of RAMP-targeted drug development.

摘要

受体活性修饰蛋白(RAMPs)与 G 蛋白偶联受体(GPCRs)相互作用,从而调节其功能,对其生理和治疗潜能具有重要意义。最近,共进化研究和正交技术筛选平台激发了人们对鉴定 RAMPs-GPCR 相互作用的兴趣。这些新的研究揭示了以前未被识别的与 RAMPs 相互作用的 GPCRs,其中许多超出了 B 类 GPCRs。这些相互作用对 GPCR 功能和生理学的影响为新的分子治疗靶点奠定了基础,依那西普的成功就是一个很好的证明。在这里,我们重点介绍了最近发现新的 RAMPs-GPCR 相互作用、人类 RAMPs-GPCR 致病突变和与 RAMPs 相关的人类病理的论文,为靶向 RAMPs 的药物开发开辟了一个新时代。

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