Serial Femtosecond Crystallography of G Protein-Coupled Receptors

被引:43
作者
Stauch, Benjamin [1 ]
Cherezov, Vadim
机构
[1] Univ Southern Calif, Dept Chem, Los Angeles, CA 90089 USA
来源
ANNUAL REVIEW OF BIOPHYSICS, VOL 47 | 2018年 / 47卷
关键词
G protein-coupled receptor; lipidic cubic phase; serial femtosecond crystallography; structure-function; X-ray free-electron laser; CRYSTALLIZING MEMBRANE-PROTEINS; LIPIDIC CUBIC PHASE; STRUCTURAL BASIS; ANOMALOUS DIFFRACTION; LCP-FRAP; STABILIZATION; STABILITY; FAMILY; ASSAY; GPCRS;
D O I
10.1146/annurev-biophys-070317-033239
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
G protein-coupled receptors (GPCRs) represent a large superfamily of membrane proteins that mediate cell signaling and regulate a variety of physiological processes in the human body. Structure-function studies of this superfamily were enabled a decade ago by multiple breakthroughs in technology that included receptor stabilization, crystallization in a membrane environment, and microcrystallography. The recent emergence of X-ray free-electron lasers (XFELs) has further accelerated structural studies of GPCRs and other challenging proteins by overcoming radiation damage and providing access to high-resolution structures and dynamics using micrometer-sized crystals. Here, we summarize key technology advancements and major milestones of GPCR research using XFELs and provide a brief outlook on future developments in the field.
引用
收藏
页码:377 / 397
页数:21
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