ECD/ETD-based Tandem Mass Spectrometry in Proteomics

被引:11
|
作者
Sun Rui-Xiang [1 ]
Dong Meng-Qiu [2 ]
Chi Hao [1 ]
Yang Bing [2 ]
Xiu Li-Yun [1 ]
Wang Le-Heng [1 ]
Fu Yan [1 ]
He Si-Min [1 ]
机构
[1] Chinese Acad Sci, Inst Comp Technol, Key Lab Intelligent Informat Proc, Beijing 100190, Peoples R China
[2] Natl Inst Biol Sci, Beijing 102206, Peoples R China
关键词
electron capture dissociation; electron transfer dissociation; collision induced dissociation; tandem mass spectrometry; computational proteomics; ELECTRON-TRANSFER DISSOCIATION; COLLISION-INDUCED DISSOCIATION; PROTEIN-SEQUENCE ANALYSIS; CAPTURE DISSOCIATION; ION-TRAP; SIDE-CHAIN; PEPTIDE; IDENTIFICATION; CELL; CATIONS;
D O I
10.3724/SP.J.1206.2009.00352
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteomics has propelled the rapid development of mass spectrometry (MS) in the past ten years. Conversely, the advancement of MS has greatly expanded the horizon of proteomics research by allowing it to address questions never touched before. Standing out among the recent technological innovations in MS are electron capture dissociation (ECD) and electron transfer dissociation (ETD). These electron-based fragmentation methods have shown a great potential for analysis of proteolytic peptides as well as intact proteins. A promising future lies ahead for ECD- or ETD-based techniques in proteomics research, especially in studies of protein post-translational modifications and top-down analysis of intact proteins. The mechanism, instrumentation and application of ECD/ETD, along with the spectral characteristics and data analysis of peptides ECD/ETD spectra were reviewed. The current issues in ECD/ETD applications or method development, the challenges for software development, and the outlook of these techniques in future research were also discussed.
引用
收藏
页码:94 / 102
页数:9
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