化学
蛋白质水解
跨膜蛋白
淀粉样前体蛋白分泌酶
小分子
合理设计
发病机制
细胞生物学
神经科学
计算生物学
阿尔茨海默病
疾病
生物化学
淀粉样前体蛋白
生物
受体
酶
医学
免疫学
遗传学
病理
作者
Jiachen Wen,Dan Liu,Linxiang Zhao
标识
DOI:10.1016/j.ejmech.2022.114169
摘要
The γ-secretase is a large transmembrane protein complex composed of four distinct units. It has aroused numerous attention over the past two decades as its intriguing role in mediating intramembrane proteolysis. γ-Secretase controls the cleavage of a broad ranged substrates, part of which have implicated in the pathogenesis of Alzheimer's disease, inflammation, and tumorigenesis. The disclosure of the atomic structure of the γ-secretase complex through cryo-EM in recent years has facilitated the understanding of its physiological roles, as well as enabled rational design of novel γ-secretase targeting molecules. This review highlights the recent progress of γ-secretase inhibitors and modulators under either clinical or preclinical stages, as well as their potential uses against various biological indications.
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