孤儿G蛋白偶联受体的细胞和分子生物学。

Da Young Oh, Kyungjin Kim, Hyuk Bang Kwon, Jae Young Seong
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引用次数: 60

摘要

G蛋白偶联受体(gpcr)超家族是最大和最多样化的膜跨越蛋白群。它通过异源三聚体G蛋白向细胞传递胞外信号,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有168个基因编码已建立的无感觉gpcr,以及207个基因预计编码新的gpcr,其天然配体仍有待鉴定,即所谓的孤儿gpcr。其中86名孤儿现在已经与新的或以前已知的分子配对,121名孤儿仍然处于孤儿状态。更好地了解GPCR的结构和分类;了解受体激活机制,依赖或独立于激动剂;加深对gpcr介导的信号转导控制的认识;适当的配体筛选系统的发展可能会提高为剩余的孤儿gpcr发现新配体的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cellular and molecular biology of orphan G protein-coupled receptors.

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.

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