化学
S-亚硝基化
蛋白质组
蛋白质组学
TCEP
硫黄
生物化学
定量蛋白质组学
胰蛋白酶
半胱氨酸
组合化学
计算生物学
酶
催化作用
有机化学
磷化氢
生物
基因
作者
Hongmei Yang,Linxu Wang,Zhaoyang Xie,Simeng Shao,Yi Wu,Weiyin Xu,Bin Gu,Bo Wang
标识
DOI:10.1016/j.chroma.2023.464162
摘要
Comprehensive sulfur-nitrosylation (SNO) proteome coverage in complex biological systems remains challenging as a result of the low level of endogenous S-nitrosylation and its chemical instability. Herein, we optimized the synthesis route of SNOTRAP (SNO trapping by triaryl phosphine) probe and the proteomics pipeline (including preventing over-alkylation, sample washing, trypsin digestion). Preventing overalkylation was found to be the key factor resulting in a higher number of identified SNO proteins by evaluating various experimental conditions. With the improved SNOTRAP-based proteomic pipeline, we achieved an improvement of ∼10-fold on identification efficiency, and identified 1181 SNO proteins (1714 SNO sites) in mouse brain, representing the largest repository of endogenous S-nitrosylation. Moreover, we identified the consensus motif of SNO sites, suggesting the correlation with local hydrophobicity, acid-base catalysis, and the surrounding secondary structures for modification of specific cysteines by NO. Collectively, we provide a universal pipeline for the high-coverage identification of low-abundance SNO proteins with high enrichment efficiency, high specificity (98%), good reproducibility, and easy implementation, contributing to the elucidation of the mechanism(s) of nitrosative stress in multiple diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI