Department of Biophysics and Free Radical Research Center, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.
J Biol Chem. 2012 Jan 27;287(5):2984-95. doi: 10.1074/jbc.M111.309062. Epub 2011 Dec 4.
Herein we describe a high-throughput fluorescence and HPLC-based methodology for global profiling of reactive oxygen and nitrogen species (ROS/RNS) in biological systems. The combined use of HPLC and fluorescence detection is key to successful implementation and validation of this methodology. Included here are methods to specifically detect and quantitate the products formed from interaction between the ROS/RNS species and the fluorogenic probes, as follows: superoxide using hydroethidine, peroxynitrite using boronate-based probes, nitric oxide-derived nitrosating species with 4,5-diaminofluorescein, and hydrogen peroxide and other oxidants using 10-acetyl-3,7-dihydroxyphenoxazine (Amplex® Red) with and without horseradish peroxidase, respectively. In this study, we demonstrate real-time monitoring of ROS/RNS in activated macrophages using high-throughput fluorescence and HPLC methods. This global profiling approach, simultaneous detection of multiple ROS/RNS products of fluorescent probes, developed in this study will be useful in unraveling the complex role of ROS/RNS in redox regulation, cell signaling, and cellular oxidative processes and in high-throughput screening of anti-inflammatory antioxidants.
在这里,我们描述了一种基于高通量荧光和 HPLC 的方法,用于对生物系统中的活性氧和氮物种(ROS/RNS)进行全局分析。HPLC 和荧光检测的结合使用是成功实施和验证该方法的关键。这里包括专门用于检测和定量 ROS/RNS 物种与荧光探针相互作用形成的产物的方法,如下所示:使用羟乙基啶检测超氧自由基,使用硼酸酯探针检测过氧亚硝酸盐,使用 4,5-二氨基荧光素检测一氧化氮衍生的亚硝化物种,使用 10-乙酰-3,7-二羟基苯并恶嗪(Amplex® Red)检测过氧化氢和其他氧化剂,分别在有和没有辣根过氧化物酶的情况下进行。在这项研究中,我们使用高通量荧光和 HPLC 方法实时监测活化巨噬细胞中的 ROS/RNS。本研究中开发的这种全局分析方法,同时检测荧光探针的多种 ROS/RNS 产物,将有助于揭示 ROS/RNS 在氧化还原调节、细胞信号转导和细胞氧化过程中的复杂作用,以及在抗炎抗氧化剂的高通量筛选中发挥作用。