G protein-coupled receptors: structure- and function-based drug discovery

被引:0
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作者
Dehua Yang
Qingtong Zhou
Viktorija Labroska
Shanshan Qin
Sanaz Darbalaei
Yiran Wu
Elita Yuliantie
Linshan Xie
Houchao Tao
Jianjun Cheng
Qing Liu
Suwen Zhao
Wenqing Shui
Yi Jiang
Ming-Wei Wang
机构
[1] Chinese Academy of Sciences,The National Center for Drug Screening, Shanghai Institute of Materia Medica
[2] Chinese Academy of Sciences,The CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica
[3] Fudan University,School of Basic Medical Sciences
[4] University of Chinese Academy of Sciences,iHuman Institute
[5] ShanghaiTech University,School of Life Science and Technology
[6] ShanghaiTech University,School of Pharmacy
[7] Fudan University,undefined
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摘要
As one of the most successful therapeutic target families, G protein-coupled receptors (GPCRs) have experienced a transformation from random ligand screening to knowledge-driven drug design. We are eye-witnessing tremendous progresses made recently in the understanding of their structure–function relationships that facilitated drug development at an unprecedented pace. This article intends to provide a comprehensive overview of this important field to a broader readership that shares some common interests in drug discovery.
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