Targeted Quantification of Glutathione/Arginine Redox Metabolism Based on a Novel Paired Mass Spectrometry Probe Approach for the Functional Assessment of Redox Status.
Zhu-Jun ZhongJing LingZhong-Ping YaoLi-Fang LiuJia-Yi ZhengGui-Zhong XinPublished in: Analytical chemistry (2024)
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- N -hydroxysuccinimidyl carbamate (AQC) and newly synthesized 2-methyl-6-aminoquinolyl- N -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.
Keyphrases
- liquid chromatography tandem mass spectrometry
- ms ms
- oxidative stress
- mass spectrometry
- nitric oxide
- electron transfer
- simultaneous determination
- high resolution
- high performance liquid chromatography
- metabolic syndrome
- healthcare
- cell proliferation
- drug delivery
- risk assessment
- emergency department
- chronic obstructive pulmonary disease
- dna damage
- skeletal muscle
- social media
- fluorescent probe
- cancer therapy
- amino acid
- living cells
- single molecule
- insulin resistance
- tandem mass spectrometry
- adverse drug
- fluorescence imaging