Levoye Angélique, Dam Julie, Ayoub Mohammed A, Guillaume Jean-Luc, Jockers Ralf
Institut Cochin, Department of Cell Biology, UMR-S 8104, 22 rue Méchain, Paris F-75014, France.
EMBO Rep. 2006 Nov;7(11):1094-8. doi: 10.1038/sj.embor.7400838.
G-protein-coupled receptors (GPCRs) are important drug targets and are involved in virtually every biological process. However, there are still more than 140 orphan GPCRs, and deciphering their function remains a priority for fundamental and clinical research. Research on orphan GPCRs has concentrated mainly on the identification of their natural ligands, whereas recent data suggest additional ligand-independent functions for these receptors. This emerging concept is connected with the observation that orphan GPCRs can heterodimerize with GPCRs that have identified ligands, and by so doing regulate the function of the latter. Pairing orphan GPCRs with their potential heterodimerization partners will have a major impact on our understanding of the extraordinary diversity offered by GPCR heterodimerization and, in addition, will constitute a novel strategy to elucidate the function of orphan receptors that needs to be added to the repertoire of 'deorphanization' strategies.
G蛋白偶联受体(GPCRs)是重要的药物靶点,几乎参与了每一个生物学过程。然而,仍有140多种孤儿GPCRs,解读它们的功能仍然是基础研究和临床研究的重点。对孤儿GPCRs的研究主要集中在鉴定其天然配体上,而最近的数据表明这些受体还具有其他不依赖配体的功能。这一新兴概念与以下观察结果相关:孤儿GPCRs可与已鉴定出配体的GPCRs形成异源二聚体,从而调节后者的功能。将孤儿GPCRs与其潜在的异源二聚化伙伴配对,将对我们理解GPCR异源二聚化所带来的非凡多样性产生重大影响,此外,这还将构成一种阐明孤儿受体功能——需要添加到“去孤儿化”策略中的一种新策略。