Oh Da Young, Kim Kyungjin, Kwon Hyuk Bang, Seong Jae Young
Laboratory of G Protein-Coupled Receptors, Korea University College of Medicine, Seoul 136-707, Korea.
Int Rev Cytol. 2006;252:163-218. doi: 10.1016/S0074-7696(06)52003-0.
The superfamily of G protein-coupled receptors (GPCRs) is the largest and most diverse group of membrane-spanning proteins. It plays a variety of roles in pathophysiological processes by transmitting extracellular signals to cells via heterotrimeric G proteins. Completion of the human genome project revealed the presence of approximately 168 genes encoding established nonsensory GPCRs, as well as 207 genes predicted to encode novel GPCRs for which the natural ligands remained to be identified, the so-called orphan GPCRs. Eighty-six of these orphans have now been paired to novel or previously known molecules, and 121 remain to be deorphaned. A better understanding of the GPCR structures and classification; knowledge of the receptor activation mechanism, either dependent on or independent of an agonist; increased understanding of the control of GPCR-mediated signal transduction; and development of appropriate ligand screening systems may improve the probability of discovering novel ligands for the remaining orphan GPCRs.
G蛋白偶联受体(GPCRs)超家族是最大且最多样化的跨膜蛋白家族。它通过异源三聚体G蛋白将细胞外信号传递给细胞,在病理生理过程中发挥多种作用。人类基因组计划的完成揭示了大约168个编码已确定的非感官GPCRs的基因的存在,以及207个预测编码新型GPCRs的基因,其天然配体仍有待确定,即所谓的孤儿GPCRs。这些孤儿GPCRs中,有86个现已与新型或先前已知的分子配对,还有121个仍有待找到其配体。更好地理解GPCRs的结构和分类;了解受体激活机制,无论其是否依赖激动剂;进一步理解GPCR介导的信号转导的调控;以及开发合适的配体筛选系统,可能会提高为其余孤儿GPCRs发现新型配体的概率。