Advances in top-down proteomics for disease biomarker discovery

被引:49
作者
Calligaris, David [1 ]
Villard, Claude [1 ]
Lafitte, Daniel [1 ]
机构
[1] Aix Marseille Univ, INSERM, Ctr Rech Oncol Biol & Oncopharmacol, Fac Pharm,UMR 911, F-13385 Marseille 5, France
关键词
Top-down; Fragmentation; Proteomics; Biomarkers; Post-translational modifications; ELECTRON-CAPTURE DISSOCIATION; IN-SOURCE DECAY; TANDEM MASS-SPECTROMETRY; COLLISIONALLY-ACTIVATED DISSOCIATION; INFRARED MULTIPHOTON DISSOCIATION; LASER-DESORPTION/IONIZATION-TIME; GAS-PHASE BASICITIES; INTACT PROTEINS; POSTTRANSLATIONAL MODIFICATIONS; SEQUENCE INFORMATION;
D O I
10.1016/j.jprot.2011.03.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Top-down mass spectrometry strategies allow identification and characterization of proteins and protein networks by direct fragmentation. These analytical processes involve a panel of fragmentation mechanisms, some of which preserve protein post-translational modifications. Thus top-down is of special interest in clinical biochemistry to probe modified proteins as potential disease biomarkers. This review describes separating methods, mass spectrometry instrumentation, bioinformatics, and theoretical aspects of fragmentation mechanisms used for top-down analysis. The biological interest of this strategy is extensively reported regarding the characterization of post-translational modifications in biochemical pathways and the discovery of biomarkers. One has to bear in mind that quantitative aspects that are beyond the focus of this review are also of critical important for biomarker discovery. The constant evolution of technologies makes top-down strategies crucial players in clinical and basic proteomics. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:920 / 934
页数:15
相关论文
共 128 条
[1]  
Adamczyk M, 1999, RAPID COMMUN MASS SP, V13, P1413, DOI 10.1002/(SICI)1097-0231(19990730)13:14<1413::AID-RCM657>3.0.CO
[2]  
2-4
[3]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[4]   Achievements and perspectives of top-down proteomics [J].
Armirotti, Andrea ;
Damonte, Gianluca .
PROTEOMICS, 2010, 10 (20) :3566-3576
[5]   Electron capture dissociation mass spectrometry in characterization of peptides and proteins [J].
Bakhtiar, Ray ;
Guan, Ziqiang .
BIOTECHNOLOGY LETTERS, 2006, 28 (14) :1047-1059
[6]   CYFRA 21-1 level predicts survival in non-small-cell lung cancer patients receiving gefitinib as third-line therapy [J].
Barlési, F ;
Tchouhadjian, C ;
Doddoli, C ;
Torre, JP ;
Astoul, P ;
Kleisbauer, JP .
BRITISH JOURNAL OF CANCER, 2005, 92 (01) :13-14
[7]   Proteomics by FTICR mass spectrometry: Top down and bottom up [J].
Bogdanov, B ;
Smith, RD .
MASS SPECTROMETRY REVIEWS, 2005, 24 (02) :168-200
[8]  
Bon C, 1998, ANN BIOL CLIN-PARIS, V56, P175
[9]   B3LYP DFT molecular orbital approach, an efficient method to evaluate the thermochemical properties of MALDI matrices [J].
Bourcier, S ;
Hoppilliard, Y .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2002, 217 (1-3) :231-244
[10]   Further studies of in-source fragmentation of peptides in matrix-assisted laser desorption-ionization [J].
Brown, RS ;
Feng, JH ;
Reiber, DC .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 1997, 169 :1-18