Integration of High Accuracy N-Terminus Identification in Peptide Sequencing and Comparative Protein Analysis Via Isothiocyanate-Based Isotope Labeling Reagent with ESI Ion-trap TOF MS

被引:14
作者
Leng, Jiapeng [1 ]
Wang, Haoyang [1 ]
Zhang, Li [1 ]
Zhang, Jing [1 ]
Wang, Hang [1 ]
Cai, Tingting [1 ]
Yao, Jinting [2 ]
Guo, Yinlong [1 ]
机构
[1] Chinese Acad Sci, Shanghai Mass Spectrometry Ctr, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
[2] Shimadzu Global COE Applicat & Tech Dev, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
4,6-dimethoxy pyrimidine-2-isothiocyanate; Isotope labeling; N-terminus identification; b1; ions; Comparative protein analysis; TANDEM MASS-SPECTROMETRY; GAS-PHASE; QUANTITATIVE PROTEOMICS; ISOLEUCINE RESIDUES; LEUCINE; DERIVATIVES; FRAGMENTATION; DIFFERENTIATION; CLEAVAGE; MALDI;
D O I
10.1007/s13361-011-0129-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A multifunctional isothiocyanate-based isotope labeling reagent, [d (0)]-/[d (6)]-4,6-dimethoxy pyrimidine-2-isothiocyanate (DMPITC), has been developed for accurate N-terminus identification in peptide sequencing and comparative protein analysis by ESI Ion-trap TOF mass spectrometry. In contrast with the conventional labeling reagent phenyl isothiocyanate (PITC), DMPITC showed more desirable properties such as rapid labeling, sensitivity enhancement, and facilitating peptide sequencing. More significantly, DMPITC-based labeling strategy possessed the capacity of higher reliable N-terminus identification owning to the high-yield b(1) ion combined with the isotope validation of 6 Da. Meanwhile, it also showed potential in differentiating isomeric residues of leucine and isoleucine at N-terminus on the basis of the relative abundance ratios between the fragment ions of their respective b(1) ions. The strategy not only allows accurate interpretation for peptide but also ensures rapid and sensitive comparative analysis for protein by direct MS analysis. Using trypsin-digested bovine serum albumin (BSA), both peptide N-terminus identification and quantitative analysis were accomplished with high accuracy, efficiency, and reproducibility. The application of DMPITC-based labeling strategy is expected to serve as a promising tool for proteome research.
引用
收藏
页码:1204 / 1213
页数:10
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