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降钙素基因相关肽(CGRP)受体的配体结合与激活

Ligand binding and activation of the CGRP receptor.

作者信息

Conner A C, Simms J, Barwell J, Wheatley M, Poyner D R

机构信息

School of Medicine, University of Swansea, Swansea SA2 8PP, UK.

出版信息

Biochem Soc Trans. 2007 Aug;35(Pt 4):729-32. doi: 10.1042/BST0350729.

Abstract

The receptor for CGRP (calcitonin gene-related peptide) is a heterodimer between a GPCR (G-protein-coupled receptor), CLR (calcitonin receptor-like receptor) and an accessory protein, RAMP1 (receptor activity-modifying protein 1). Models have been produced of RAMP1 and CLR. It is likely that the C-terminus of CGRP interacts with the extracellular N-termini of CLR and RAMP1; the extreme N-terminus of CLR is particularly important and may interact directly with CGRP and also with RAMP1. The N-terminus of CGRP interacts with the TM (transmembrane) portion of the receptor; the second ECL (extracellular loop) is especially important. Receptor activation is likely to involve the relative movements of TMs 3 and 6 to create a G-protein-binding pocket, as in Family A GPCRs. Pro(321) in TM6 appears to act as a pivot. At the base of TMs 2 and 3, Arg(151), His(155) and Glu(211) may form a loose equivalent of the Family A DRY (Asp-Arg-Tyr) motif. Although the details of this proposed activation mechanism clearly do not apply to all Family B GPCRs, the broad outlines may be conserved.

摘要

降钙素基因相关肽(CGRP)的受体是一种异二聚体,由G蛋白偶联受体(GPCR)降钙素受体样受体(CLR)和辅助蛋白受体活性修饰蛋白1(RAMP1)组成。已构建出RAMP1和CLR的模型。CGRP的C末端可能与CLR和RAMP1的细胞外N末端相互作用;CLR的极端N末端尤为重要,可能直接与CGRP以及RAMP1相互作用。CGRP的N末端与受体的跨膜(TM)部分相互作用;第二个细胞外环(ECL)尤为重要。受体激活可能涉及跨膜螺旋3(TM3)和跨膜螺旋6(TM6)的相对移动以形成一个G蛋白结合口袋,就像A类GPCR一样。TM6中的Pro(321)似乎起到了枢轴的作用。在TM2和TM3的底部,Arg(151)、His(155)和Glu(211)可能形成一个类似于A类DRY(天冬氨酸 - 精氨酸 - 酪氨酸)基序的松散结构。尽管这个提出的激活机制的细节显然并不适用于所有B类GPCR,但大致轮廓可能是保守的。

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