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减轻NADPH氧化酶2活性作为抑制过氧亚硝酸盐形成的策略。

Mitigation of NADPH Oxidase 2 Activity as a Strategy to Inhibit Peroxynitrite Formation.

作者信息

Zielonka Jacek, Zielonka Monika, VerPlank Lynn, Cheng Gang, Hardy Micael, Ouari Olivier, Ayhan Mehmet Menaf, Podsiadły Radosław, Sikora Adam, Lambeth J David, Kalyanaraman Balaraman

机构信息

From the Department of Biophysics and Free Radical Research Center, Medical College of Wisconsin, Milwaukee, Wisconsin 53226,

From the Department of Biophysics and Free Radical Research Center, Medical College of Wisconsin, Milwaukee, Wisconsin 53226.

出版信息

J Biol Chem. 2016 Mar 25;291(13):7029-44. doi: 10.1074/jbc.M115.702787. Epub 2016 Feb 2.

Abstract

Using high throughput screening-compatible assays for superoxide and hydrogen peroxide, we identified potential inhibitors of the NADPH oxidase (Nox2) isoform from a small library of bioactive compounds. By using multiple probes (hydroethidine, hydropropidine, Amplex Red, and coumarin boronate) with well defined redox chemistry that form highly diagnostic marker products upon reaction with superoxide (O2 (̇̄)), hydrogen peroxide (H2O2), and peroxynitrite (ONOO(-)), the number of false positives was greatly decreased. Selected hits for Nox2 were further screened for their ability to inhibit ONOO(-)formation in activated macrophages. A new diagnostic marker product for ONOO(-)is reported. We conclude that the newly developed high throughput screening/reactive oxygen species assays could also be used to identify potential inhibitors of ONOO(-)formed from Nox2-derived O2 (̇̄)and nitric oxide synthase-derived nitric oxide.

摘要

通过使用与高通量筛选兼容的超氧化物和过氧化氢检测方法,我们从小分子生物活性化合物库中鉴定出了NADPH氧化酶(Nox2)亚型的潜在抑制剂。通过使用具有明确氧化还原化学性质的多种探针(羟基乙啶、羟基丙啶、Amplex Red和香豆素硼酸酯),这些探针在与超氧化物(O2 (̇̄))、过氧化氢(H2O2)和过氧亚硝酸盐(ONOO(-))反应时会形成高度诊断性的标记产物,从而大大减少了假阳性的数量。对筛选出的Nox2命中化合物进一步筛选其抑制活化巨噬细胞中ONOO(-)形成的能力。报道了一种新的ONOO(-)诊断标记产物。我们得出结论,新开发的高通量筛选/活性氧检测方法也可用于鉴定由Nox2衍生的O2 (̇̄)和一氧化氮合酶衍生的一氧化氮形成的ONOO(-)的潜在抑制剂。

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