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一种适用于高通量筛选线粒体酰胺氧化还原酶(mARC)底物和抑制剂的活性测定新设计。

New Design of an Activity Assay Suitable for High-Throughput Screening of Substrates and Inhibitors of the Mitochondrial Amidoxime Reducing Component (mARC).

机构信息

Pharmaceutical Institute - Medicinal Chemistry, Kiel University, Gutenbergstraße 76, 24118 Kiel, Germany.

Zoological Institute - Structural Biology, Kiel University, Am Botanischen Garten 9, 24118 Kiel, Germany.

出版信息

Anal Chem. 2023 Aug 22;95(33):12452-12458. doi: 10.1021/acs.analchem.3c02109. Epub 2023 Aug 7.

Abstract

The mitochondrial amidoxime-reducing component (mARC) is one of the simplest molybdenum-containing enzymes. mARC is among a few known reducing enzymes playing an important role in drug metabolism in mammals. Here, an assay based on the fluorescence of NADH is reported for the rapid detection of substrates and potential inhibitors of mARC. So far unknown inhibitors might be useful for the development of drugs assigned to nonalcoholic fatty liver disease (NAFLD) and similar diseases. Kinetics of reactions catalyzed by mARC can be recorded with high sensitivity and precision. On a microtiter plate scale, the assay presented could be applied for high-throughput screening of substance libraries and detection of novel mARC substrate candidates. For instance, molnupiravir was also identified as a new substrate by this assay. For better comparison for such substances, the inhibitor or substrate-to-BAO ratio was introduced. After normalization of enzyme activities to the standard benzamidoxime, substrates can reproducibly be classified.

摘要

线粒体 amidoxime 还原酶(mARC)是最简单的钼酶之一。mARC 是哺乳动物中参与药物代谢的少数几种已知还原酶之一。本研究报道了一种基于 NADH 荧光的快速检测 mARC 底物和潜在抑制剂的方法。迄今为止未知的抑制剂可能有助于开发用于治疗非酒精性脂肪性肝病(NAFLD)和类似疾病的药物。mARC 催化的反应动力学可以高灵敏度和高精度进行记录。在微孔板规模上,本研究提出的方法可用于物质文库的高通量筛选和新型 mARC 底物候选物的检测。例如,莫努匹韦也被该方法鉴定为新的底物。为了更好地比较此类物质,引入了抑制剂或底物与 BAO 的比值。在将酶活性标准化到标准苯甲脒肟后,可以重复地对底物进行分类。

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