阿佩林
G蛋白偶联受体
功能选择性
兴奋剂
受体
痛苦
信号转导
生物
药理学
内科学
细胞生物学
医学
生物化学
政治
政治学
法学
作者
Qiu Sun,Xiaowen Tian,Lun Tan,Yan Deng,Sicen Liu,Yixiao Xiong,Yuying Feng,Yujia Wang,Lele Zhang,Jiayi Zhu,Huan Xiao,Zhenhua Shao,Yingqiang Guo,Wei Yan,Tao Li,Liang Ouyang
标识
DOI:10.1073/pnas.2423432122
摘要
-protein-biased APLNR agonist CMF-019 and developed a biased chemical space remodeling approach to identify exclusive G-protein-biased agonists targeting APLNR. These agonists exhibited enhanced Gi-protein-biased function and protective effects in both in vitro and in vivo. Our findings not only enhance comprehension of APLNR-biased agonism but also establish drug design strategies for modifying and reshaping biased chemical landscapes in other G-protein-coupled receptors (GPCRs).
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