中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Chapter 1 - Progress in GPCR structure determination

文献类型:专著章节

作者Qu, Xiangli1,4,5; Wang, Dejian1,4,5; Wu, Beili2,3,4,5
发表日期2019-09-13
出处GPCRs: Structure, Function, and Drug Discovery
出版地125 London Wall, London EC2Y 5AS, United Kingdom
ISBN号978-0-12-816228-6
出版者Academic Press
英文摘要

G protein-coupled receptors (GPCRs) are widely distributed in the human body and trigger cellular responses to a variety of extracellular stimuli. The diverse functions of GPCRs make these receptors key players in numerous physiological regulations and valuable drug targets for many diseases. The GPCR structures are important for understanding the molecular mechanisms of GPCR signaling and enable structure-based drug discovery. Recent advances in GPCR structure determination have provided valuable insights into ligand recognition, receptor activation, and signaling transduction of these receptors. Here we summarize the recent progress, techniques, and discoveries in GPCR structural studies to elucidate the successful strategies for GPCR structure determination and structural basis of GPCR function.

DOI标识10.1016/B978-0-12-816228-6.00001-5
源URL[http://119.78.100.183/handle/2S10ELR8/309264]  
专题新药研究国家重点实验室
作者单位1.State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Pudong, Shanghai, China
2.CAS Center for Excellence in Biomacromolecules, Chinese Academy of Sciences, Beijing, China
3.School of Life Science and Technology, ShanghaiTech University, Pudong, Shanghai, China
4.CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Pudong, Shanghai, China
5.University of Chinese Academy of Sciences, Beijing, China
推荐引用方式
GB/T 7714
Qu, Xiangli,Wang, Dejian,Wu, Beili. Chapter 1 - Progress in GPCR structure determination. 125 London Wall, London EC2Y 5AS, United Kingdom:Academic Press,2019.

入库方式: OAI收割

来源:上海药物研究所

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