雷公藤醇
邻苯二酚-O-甲基转移酶
化学
甲基转移酶
儿茶酚
半胱氨酸
酶
生物化学
多巴胺
药理学
生物
甲基化
内分泌学
基因型
DNA
基因
细胞凋亡
作者
Huajun Guo,Yang Yang,Qi Zhang,Jie-Ren Deng,Ying Yang,Shuqi Li,Pui-Kin So,Thomas Chuen Lam,Man Leung Wong,Qian Zhao
标识
DOI:10.1021/acschembio.2c00011
摘要
Natural product celastrol is known to have various biological activities, yet its molecular targets that correspond to many activities remain unclear. Here, we used multiple mass-spectrometry-based approaches to identify catechol-O-methyltransferase (COMT) as a major binding target of celastrol and characterized their interaction comprehensively. Celastrol was found to inhibit the enzymatic activity of COMT and increased the dopamine level in neuroendocrine chromaffin cells significantly. Our study not only revealed a novel binding target of celastrol but also provided a new scaffold and cysteine hot spot for developing new generation COMT inhibitors in combating neurological disorders.
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