压电1
药物发现
虚拟筛选
离子通道
计算生物学
纳米技术
药品
功能(生物学)
生物
神经科学
生物信息学
细胞生物学
药理学
材料科学
遗传学
受体
机械敏感通道
出处
期刊:Annual Review of Pharmacology and Toxicology
[Annual Reviews]
日期:2019-08-27
卷期号:60 (1): 195-218
被引量:116
标识
DOI:10.1146/annurev-pharmtox-010919-023703
摘要
The mechanically activated Piezo channels, including Piezo1 and Piezo2 in mammals, function as key mechanotransducers for converting mechanical force into electrochemical signals. This review highlights key evidence for the potential of Piezo channel drug discovery. First, both mouse and human genetic studies have unequivocally demonstrated the prominent role of Piezo channels in various mammalian physiologies and pathophysiologies, validating their potential as novel therapeutic targets. Second, the cryo-electron microscopy structure of the 2,547-residue mouse Piezo1 trimer has been determined, providing a solid foundation for studying its structure-function relationship and drug action mechanisms and conducting virtual drug screening. Third, Piezo1 chemical activators, named Yoda1 and Jedi1/2, have been identified through high-throughput screening assays, demonstrating the drugability of Piezo channels. However, the pharmacology of Piezo channels is in its infancy. By establishing an integrated drug discovery platform, we may hopefully discover and develop a fleet of Jedi masters for battling Piezo-related human diseases.
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