当前位置: X-MOL 学术Annu. Rev. Biophys. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Serial Femtosecond Crystallography of G Protein–Coupled Receptors
Annual Review of Biophysics ( IF 12.4 ) Pub Date : 2018-05-24 00:00:00 , DOI: 10.1146/annurev-biophys-070317-033239
Benjamin Stauch 1 , Vadim Cherezov 1
Affiliation  

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.

中文翻译:


G 蛋白偶联受体的连续飞秒晶体学

G 蛋白偶联受体 (GPCR) 代表了一个大型膜蛋白超家族,可介导细胞信号传导并调节人体内的各种生理过程。十年前,由于受体稳定、膜环境中的结晶和微晶体学等技术的多项突破,该超家族的结构功能研究得以实现。最近出现的 X 射线自由电子激光器 (XFEL) 通过克服辐射损伤并使用微米大小的晶体提供高分辨率结构和动力学,进一步加速了 GPCR 和其他具有挑战性的蛋白质的结构研究。在这里,我们总结了使用 XFEL 进行 GPCR 研究的关键技术进步和主要里程碑,并对该领域的未来发展进行了简要展望。

更新日期:2018-05-24
down
wechat
bug