Levoye Angélique, Jockers Ralf
Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Department of Cell Biology, Paris, France.
Drug Discov Today. 2008 Jan;13(1-2):52-8. doi: 10.1016/j.drudis.2007.09.011. Epub 2007 Nov 19.
G protein-coupled receptors (GPCRs) are well-known drug targets. However, a question mark remains for the more than 100 orphan GPCRs as current deorphanisation strategies failed to identify specific ligands for these receptors. Recent advances have shown that orphan GPCRs may have important functions that are ligand-independent. Orphan GPCRs can modulate the function of well-defined drug targets such as GPCRs with identified ligands and neurotransmitter transporters though physical association with those molecules. Thus, compounds that bind to orphan GPCRs and allosterically regulate the function of the interacting partner or even disrupt the interaction with the latter could become new drugs.
G蛋白偶联受体(GPCRs)是众所周知的药物靶点。然而,对于100多种孤儿GPCRs来说,仍然存在一个问号,因为目前的去孤儿化策略未能识别出这些受体的特异性配体。最近的进展表明,孤儿GPCRs可能具有与配体无关的重要功能。孤儿GPCRs可以通过与已确定配体的GPCRs和神经递质转运体等明确的药物靶点分子发生物理缔合,来调节其功能。因此,与孤儿GPCRs结合并变构调节相互作用伙伴功能甚至破坏与后者相互作用的化合物可能成为新药。