Lismont Celien, Walton Paul A, Fransen Marc
Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, University of Leuven - KU Leuven, Herestraat 49 - box 601, Leuven, 3000, Belgium.
Department of Anatomy and Cell Biology, University of Western Ontario, London, Canada.
Methods Mol Biol. 2017;1595:151-164. doi: 10.1007/978-1-4939-6937-1_14.
To gain additional insight into how specific cell organelles may participate in redox signaling, it is essential to have access to tools and methodologies that are suitable to monitor spatiotemporal differences in the levels of different reactive oxygen species (ROS) and the oxidation state of specific redox couples. Over the years, the use of genetically encoded fluorescent redox indicators with a ratiometric readout has constantly gained in popularity because they can easily be targeted to various subcellular compartments and monitored in real time in single cells. Here we provide step-by-step protocols and tips for the successful use of roGFP2, a redox-sensitive variant of the enhanced green fluorescent protein, to monitor changes in glutathione redox balance and hydrogen peroxide homeostasis in the cytosol, peroxisomes, and mitochondria of mammalian cells.
为了更深入了解特定细胞器如何参与氧化还原信号传导,必须有合适的工具和方法来监测不同活性氧(ROS)水平的时空差异以及特定氧化还原对的氧化状态。多年来,具有比率读数的基因编码荧光氧化还原指示剂的使用越来越普遍,因为它们可以轻松靶向各种亚细胞区室并在单细胞中进行实时监测。在这里,我们提供了逐步方案和提示,以成功使用增强型绿色荧光蛋白的氧化还原敏感变体roGFP2,来监测哺乳动物细胞胞质溶胶、过氧化物酶体和线粒体中谷胱甘肽氧化还原平衡和过氧化氢稳态的变化。