The GPCR Network: a large-scale collaboration to determine human GPCR structure and function

被引:227
作者
Stevens, Raymond C. [1 ]
Cherezov, Vadim [1 ]
Katritch, Vsevolod [1 ]
Abagyan, Ruben [2 ,3 ]
Kuhn, Peter [4 ]
Rosen, Hugh [5 ,6 ]
Wuethrich, Kurt [1 ,7 ]
机构
[1] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[3] San Diego Supercomp Ctr, La Jolla, CA 92093 USA
[4] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[5] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
[6] Scripps Res Inst, Scripps Res Inst Mol Screening Ctr, La Jolla, CA 92037 USA
[7] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-COUPLED RECEPTORS; A(2A) ADENOSINE RECEPTOR; MUSCARINIC ACETYLCHOLINE-RECEPTOR; HISTAMINE H-1 RECEPTOR; CRYSTAL-STRUCTURE; OPIOID RECEPTOR; SUBTYPE-SELECTIVITY; MEMBRANE-PROTEINS; LIGAND DISCOVERY; COMPLEX;
D O I
10.1038/nrd3859
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
G protein-coupled receptors (GPCRs) are targeted by similar to 30-40% of marketed drugs, and their key roles in normal physiology and in disease demonstrate that an understanding of their structure and function is valuable to researchers in both basic science and drug discovery. However, until recently, detailed structural information on this protein family was limited by challenges in X-ray crystallographic analysis of such membrane proteins. The GPCR Network was created in 2010 with the goal of structurally characterizing 15-25 representative human GPCRs within 5 years, based on an active outreach programme addressing an interdisciplinary community of scientists interested in GPCR structure, chemistry and biology. Here, we provide an overview of how this collaborative effort has enabled the structural determination and characterization of eight human GPCRs so far, and discuss some of the challenges that remain in gaining more detailed insights into structure-function relationships in this receptor superfamily.
引用
收藏
页码:25 / 34
页数:10
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