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寻找孤儿G蛋白偶联受体的功能——超越寻找内源性配体

Hunting for the function of orphan GPCRs - beyond the search for the endogenous ligand.

作者信息

Ahmad Raise, Wojciech Stefanie, Jockers Ralf

机构信息

Institut Cochin, INSERM, Paris, France.

CNRS UMR 8104, Paris, France.

出版信息

Br J Pharmacol. 2015 Jul;172(13):3212-28. doi: 10.1111/bph.12942. Epub 2014 Dec 15.

Abstract

Seven transmembrane-spanning proteins (7TM), also called GPCRs, are among the most versatile and evolutionary successful protein families. Out of the 400 non-odourant members identified in the human genome, approximately 100 remain orphans that have not been matched with an endogenous ligand. Apart from the classical deorphanization strategies, several alternative strategies provided recent new insights into the function of these proteins, which hold promise for high therapeutic potential. These alternative strategies consist of the phenotypical characterization of organisms silenced or overexpressing orphan 7TM proteins, the search for constitutive receptor activity and formation of protein complexes including 7TM proteins as well as the development of synthetic, surrogate ligands. Taken together, a variety of ligand-independent functions can be attributed to orphan 7TM proteins that range from constitutive activity to complex formation with other proteins and include 'true' orphans for which no ligand exist and 'conditional' orphans that behave like orphans in the absence of ligand and as non-orphans in the presence of ligand.

摘要

七次跨膜蛋白(7TM),也被称为G蛋白偶联受体(GPCR),是最具多功能性且在进化上最为成功的蛋白质家族之一。在人类基因组中已鉴定出的400种非嗅觉成员中,约有100种仍是孤儿受体,尚未找到与之匹配的内源性配体。除了传统的孤儿受体鉴定策略外,一些替代策略为这些蛋白质的功能提供了新的见解,具有很高的治疗潜力。这些替代策略包括对沉默或过表达孤儿7TM蛋白的生物体进行表型特征分析、寻找组成型受体活性以及形成包含7TM蛋白的蛋白质复合物,以及开发合成替代配体。综上所述,孤儿7TM蛋白具有多种不依赖配体的功能,从组成型活性到与其他蛋白质形成复合物不等,包括不存在配体的“真正”孤儿受体和在无配体时表现为孤儿受体、有配体时表现为非孤儿受体的“条件性”孤儿受体。

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