State Key Laboratory of Natural Medicines, Department of Chinese Medicines Analysis, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
State Key Laboratory of Chemical Biology and Drug Discovery, Research Centre for Chinese Medicine Innovation, Food Safety and Technology Research Centre and Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon 999077, China.
Anal Chem. 2024 Jun 18;96(24):9885-9893. doi: 10.1021/acs.analchem.4c00732. Epub 2024 Jun 7.
Glutathione (GSH) redox control and arginine metabolism are critical in regulating the physiological response to injury and oxidative stress. Quantification assessment of the GSH/arginine redox metabolism supports monitoring metabolic pathway shifts during pathological processes and their linkages to redox regulation. However, assessing the redox status of organisms with complex matrices is challenging, and single redox molecule analysis may not be accurate for interrogating the redox status in cells and in vivo. Herein, guided by a paired derivatization strategy, we present a new ultraperformance liquid chromatography tandem mass spectrometry (UPLC-MS/MS)-based approach for the functional assessment of biological redox status. Two structurally analogous probes, 6-aminoquinolyl--hydroxysuccinimidyl carbamate (AQC) and newly synthesized 2-methyl-6-aminoquinolyl--hydroxysuccinimidyl carbamate (MeAQC), were set for paired derivatization. The developed approach was successfully applied to LPS-stimulated RAW 264.7 cells and HDM-induced asthma mice to obtain quantitative information on GSH/arginine redox metabolism. The results suggest that the redox status was remarkably altered upon LPS and HDM stimulation. We expect that this approach will be of good use in a clinical biomarker assay and potential drug screening associated with redox metabolism, oxidative damage, and redox signaling.
谷胱甘肽 (GSH) 氧化还原调控和精氨酸代谢在调节损伤和氧化应激的生理反应中至关重要。GSH/精氨酸氧化还原代谢的定量评估支持在病理过程中监测代谢途径的变化及其与氧化还原调控的联系。然而,评估具有复杂基质的生物体的氧化还原状态具有挑战性,并且单个氧化还原分子分析可能无法准确地探究细胞和体内的氧化还原状态。在此,我们以配对衍生策略为指导,提出了一种新的基于超高效液相色谱串联质谱 (UPLC-MS/MS) 的方法,用于功能评估生物氧化还原状态。两种结构类似的探针,6-氨基喹啉基 -N- 羟基琥珀酰亚胺基碳酸酯 (AQC) 和新合成的 2-甲基-6-氨基喹啉基 -N- 羟基琥珀酰亚胺基碳酸酯 (MeAQC),被设定用于配对衍生化。所开发的方法成功地应用于 LPS 刺激的 RAW 264.7 细胞和 HDM 诱导的哮喘小鼠,以获得关于 GSH/精氨酸氧化还原代谢的定量信息。结果表明,LPS 和 HDM 刺激后氧化还原状态发生了显著改变。我们期望这种方法将在与氧化还原代谢、氧化损伤和氧化还原信号相关的临床生物标志物测定和潜在药物筛选中得到很好的应用。