Jacobs Lianne J H C, Hoehne Michaela N, Riemer Jan
Institute of Biochemistry, Redox Biochemistry, University of Cologne, Zuelpicher Str. 47a/R. 3.49, 50674 Cologne, Germany.
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, 50931 Cologne, Germany.
Bio Protoc. 2022 Oct 20;12(20). doi: 10.21769/BioProtoc.4538.
Depending on its local concentration, hydrogen peroxide (HO) can serve as a cellular signaling molecule but can also cause damage to biomolecules. The levels of H O are influenced by the activity of its generator sites, local antioxidative systems, and the metabolic state of the cell. To study and understand the role of HO in cellular signaling, it is crucial to assess its dynamics with high spatiotemporal resolution. Measuring these subcellular HO dynamics has been challenging. However, with the introduction of the super sensitive pH-independent genetically encoded fluorescent HOsensor HyPer7, many limitations of previous measurement approaches could be overcome. Here, we describe a method to measure local HO dynamics in intact human cells, utilizing the HyPer7 sensor in combination with a microscopic multi-mode microplate reader. Graphical abstract:
根据其局部浓度,过氧化氢(HO)可以作为一种细胞信号分子,但也会对生物分子造成损伤。HO的水平受其产生位点的活性、局部抗氧化系统以及细胞代谢状态的影响。为了研究和理解HO在细胞信号传导中的作用,以高时空分辨率评估其动态变化至关重要。测量这些亚细胞HO动态变化具有挑战性。然而,随着超灵敏的不依赖pH的基因编码荧光HO传感器HyPer7的引入,以往测量方法的许多局限性得以克服。在此,我们描述一种利用HyPer7传感器结合显微多模式微孔板读数器来测量完整人类细胞中局部HO动态变化的方法。图形摘要: