甲基乙二醛
乳糖谷胱甘肽裂解酶
糖基化
小分子
酶
生物化学
谷胱甘肽
药物发现
限制
功能(生物学)
化学
计算生物学
机制(生物学)
高通量筛选
药理学
生物
细胞生物学
受体
哲学
工程类
认识论
机械工程
作者
Yujiao He,Chunyan Zhou,Mao Lin Huang,Chunyan Tang,Xiao Liu,Yan Yue,Qingchun Diao,Zhe-Bin Zheng,Deming Liu
标识
DOI:10.1016/j.biopha.2020.110663
摘要
The glyoxalase system is a ubiquitous enzymatic network which plays important roles in biological life. It consists of glyoxalase 1 (GLO1), glyoxalase 2 (GLO2), and reduced glutathione (GSH), which perform an essential metabolic function in cells by detoxifying methylglyoxal (MG) and other endogenous harmful metabolites into non-toxic d-lactate. MG and MG-derived advanced glycation endproducts (AGEs) are associated with various diseases, such as diabetes, cardiovascular disease, neurodegenerative disorders and cancer, and GLO1 is a key rate-limiting enzyme in the anti-glycation defense. The abnormal activity and expression of GLO1 in various diseases make this enzyme a promising target for drug design and development. This review focuses on the regulatory mechanism of GLO1 in diverse pathogenic conditions with a thorough discussion of GLO1 regulators since their discovery, including GLO1 activators and inhibitors. The different classes, chemical structure and structure-activity relationship are embraced. Moreover, assays for the discovery of small molecule regulators of the glyoxalase system are also introduced in this article. Compared with spectrophotometer-based assay, microplate-based assay is a more simple, rapid and quantitative high-throughput method. This review will be useful to design novel and potent GLO1 regulators and hopefully provide a convenient reference for researchers.
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