Department of Chemistry and Bridge Institute, University of Southern California, Los Angeles, California 90089, USA; email:
Annu Rev Biophys. 2018 May 20;47:377-397. doi: 10.1146/annurev-biophys-070317-033239. Epub 2018 Mar 15.
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.
G 蛋白偶联受体 (GPCRs) 是一大类膜蛋白超家族,介导细胞信号转导,调节人体多种生理过程。该超家族的结构-功能研究得益于十年前多项技术突破,包括受体稳定化、在膜环境中结晶和微晶体学。最近 X 射线自由电子激光 (XFEL) 的出现通过克服辐射损伤并使用微米级晶体提供了获取高分辨率结构和动态信息的途径,进一步加速了 GPCR 和其他具有挑战性的蛋白质的结构研究。本文总结了使用 XFEL 进行 GPCR 研究的关键技术进展和主要里程碑,并对该领域的未来发展进行了简要展望。