黄嘌呤氧化酶
化学
黄嘌呤
毛细管电泳
类黄酮
槲皮素
酶
酶分析
色谱法
基质(水族馆)
高尿酸血症
生物杀虫素A
尿酸
立体化学
生物化学
抗氧化剂
医学
大豆黄酮
染料木素
内科学
海洋学
地质学
作者
Zhaoyu Wu,Hao Zhang,Feng Li,Feng Yang
标识
DOI:10.1002/elps.202000083
摘要
Abstract Xanthine oxidase (XOD) is a key enzyme in the human body to produce uric acid, and its inhibitor can be used for the treatment of hyperuricemia and gout. In this study, an online CE‐based XOD immobilized enzyme microreactor (IMER) was developed for the enzyme kinetics assays and inhibitor screening. After 30 consecutive runs, the XOD activity remained about 95.6% of the initial immobilized activity. The Michaelis–Menten constant ( K m ) of the immobilized XOD was determined as 0.39 mM using xanthine as substrate. The half‐maximal inhibitory concentration and inhibition constant of the known inhibitor 4‐aminopyrazolo[3,4‐d]pyrimidine on XOD were determined as 11.9 and 5.2 μM, respectively. Then, the developed method was applied to evaluate the XOD inhibitory activity of 10 flavonoids, which indicated that dihydroquercetin, quercetin, biochanin A, and epicatechin had significant inhibitory effect on XOD. In addition, molecular docking results verified that the binding energy of the flavonoids with enzyme were in line with their inhibitory activity determined by XOD–IMER. Therefore, the developed XOD–IMER is a potential tool for the primary screening of XOD inhibitors from natural products.
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