Gold Nanoparticle Enrichment Method for Identifying S-Nitrosylation and S-Glutathionylation Sites in Proteins

被引:56
作者
Faccenda, Adam [1 ]
Bonham, Christopher A. [1 ]
Vacratsis, Panayiotis O. [1 ]
Zhang, Xueji [2 ,3 ]
Mutus, Bulent [1 ]
机构
[1] Univ Windsor, Dept Chem & Biochem, Windsor, ON N9B 3P4, Canada
[2] World Precis Instruments, Sarasota, FL 34240 USA
[3] Univ Sci & Technol Beijing, Sch Appl Sci, Beijing 100083, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
DISULFIDE-ISOMERASE; MASS-SPECTROMETRY; NITRIC-OXIDE; IDENTIFICATION; NITROSOTHIOLS; CELLS; THIOREDOXIN; YVH1; NO;
D O I
10.1021/ja103591v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present a simple method by which gold nanoparticles (AuNPs) are used to simultaneously isolate and enrich for free or modified thiol-containing peptides, thus facilitating the identification of protein S-modification sites. Here, protein disulfide isomerase (PDI) and dual specificity phosphatase 12 (DUSP12 or hYVH1) were S-nitrosylated or S-glutathionylated, their free thiols differentially alkylated, and subjected to proteolysis. AuNPs were added to the digests, and the AuNP-bound peptides were isolated by centrifugation and released by thiol exchange. These AuNP-bound peptides were analyzed by MALDI-TOF mass spectrometry revealing that AuNPs result in a significant enrichment of free thiol-containing as well as S-nitrosylated, S-glutathionylated, and S-alkylated peptides, leading to the unequivocal assignment of thiols susceptible to modification.
引用
收藏
页码:11392 / 11394
页数:3
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