| Autor: |
Li Z; Department of Pediatrics, Peking University First Hospital, Beijing, China., Huang Y; Department of Pediatrics, Peking University First Hospital, Beijing, China., Lv B; Department of Pediatrics, Peking University First Hospital, Beijing, China., Du J; Department of Pediatrics, Peking University First Hospital, Beijing, China., Yang J; State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences, Beijing, Beijing Institute of Lifeomics, Beijing, China., Fu L; State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences, Beijing, Beijing Institute of Lifeomics, Beijing, China., Jin H; Department of Pediatrics, Peking University First Hospital, Beijing, China.; State Key Laboratory of Vascular Homeostasis and Remodeling, Peking University, Beijing, China. |
| Abstrakt: |
Significance: Gasotransmitters, including nitric oxide (NO), hydrogen sulfide (H 2 S) and sulfur dioxide (SO 2 ), participate in various cellular processes via corresponding oxidative posttranslational modifications (oxiPTMs) of specific cysteines. Recent Advances: Accumulating evidence has clarified the mechanisms underlying the formation of oxiPTMs derived from gasotransmitters and their biological functions in multiple signal pathways. Because of the specific existence and functional importance, determining the sites of oxiPTMs in cysteine is crucial in biology. Recent advances in the development of selective probes, together with upgraded mass spectrometry (MS)-based proteomics, have enabled the quantitative analysis of cysteinome. To date, several cysteine residues have been identified as gasotransmitter targets. Critical Issues: To clearly understand the underlying mechanisms for gasotransmitter-mediated biological processes, it is important to identify modified targets. In this review, we summarize the chemical formation and biological effects of gasotransmitter-dependent oxiPTMs and highlight the state-of-the-art detection methods. Future Directions: Future studies in this field should aim to develop the next generation of probes for in situ labeling to improve spatial resolution and determine the dynamic change of oxiPTMs, which can lay the foundation for research on the molecular mechanisms and clinical translation of gasotransmitters. Antioxid. Redox Signal. 40, 145-167. |
