S1PR1型
鞘氨醇-1-磷酸受体
鞘氨醇
受体
1-磷酸鞘氨醇
细胞生物学
化学
机制(生物学)
生物
生物化学
癌症研究
血管内皮生长因子
哲学
认识论
血管内皮生长因子A
血管内皮生长因子受体
作者
Wei Gao,Shiyi Gan,Mengting Zhang,Asuka Inoue,Mengting Xie,Huan He,Huan Zhu,Shanshan Guo,Chen Qiu,Di Chang,Jinling Yu,Zhuo Deng,Fang Ye,Shiliang Li,Jian Zhang,Zhenjiang Zhao,Mengzhu Xue,Bernard Ofosuhene,Yufang Xu,Honghuang Lin
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2024-03-03
标识
DOI:10.1101/2024.03.02.583092
摘要
Abstract S1PR4 is one of five subtypes of sphingosine 1-phosphate receptors (S1PRs) that regulate immune cell functioning, with functional distinctions to other subtypes. S1PR1-targeted modulators caused serious cardiac and vascular adverse effects because S1PR1 was expressed throughout the whole body. Since S1PR4 was only expressed in lung and lymphoid cells, S1PR4-targeted modulators might not trigger these side effects. However, the development of S1PR4-specific agonists is greatly hindered because of the lack of activated S1PR4 structure. Here, we resolved cryo-EM structures of activated S1PR4 and revealed the structural mechanism of ligand recognition, receptor activation, and Gα i coupling. Our results offered structural templates for the development of selective S1PR4 agonists with improved safety profiles.
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