Applications of molecular replacement to G protein-coupled receptors

被引:3
作者
Kruse, Andrew C. [1 ]
Manglik, Aashish [1 ]
Kobilka, Brian K. [1 ]
Weis, William I. [1 ]
机构
[1] Stanford Univ, Stanford, CA 94305 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY | 2013年 / 69卷
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
molecular replacement; G protein-coupled receptors; GPCRs; membrane proteins; CRYSTAL-STRUCTURE; MEMBRANE-PROTEINS; SEROTONIN RECEPTORS; CRYSTALLOGRAPHY; CRYSTALLIZATION; COMPLEX;
D O I
10.1107/S090744491301322X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
G protein-coupled receptors (GPCRs) are a large class of integral membrane proteins involved in regulating virtually every aspect of human physiology. Despite their profound importance in human health and disease, structural information regarding GPCRs has been extremely limited until recently. With the advent of a variety of new biochemical and crystallographic techniques, the structural biology of GPCRs has advanced rapidly, offering key molecular insights into GPCR activation and signal transduction. To date, almost all GPCR structures have been solved using molecular-replacement techniques. Here, the unique aspects of molecular replacement as applied to individual GPCRs and to signaling complexes of these important proteins are discussed.
引用
收藏
页码:2287 / 2292
页数:6
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