Sequit:: software for de novo peptide sequencing by matrix-assisted laser desorption/ionization post-source decay mass spectrometry

被引:24
作者
Demine, R [1 ]
Walden, P [1 ]
机构
[1] Humboldt Univ, Charite Univ Med Berlin, Dept Dermatol & Allergy, D-10117 Berlin, Germany
关键词
D O I
10.1002/rcm.1420
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Peptide sequencing by mass spectrometry is gaining increasing importance for peptide chemistry and proteomics. However, available tools for interpreting matrix-assisted laser desorption/ ionization post-source decay (MALDI-PSD) mass spectra depend on databases, and identify peptides by matching experimental data with spectra calculated from database sequences. This severely obstructs the identification of proteins and peptides not listed in databases or of variations, e.g. mutated proteins. The development of a new computer program for databaseindependent peptide sequencing by MALDI-PSD mass spectrometry is reported here. This computer program was validated by the determination of the correct sequences for various peptides including sequences listed in the sequence databases, but also for peptides that deviate from database sequences or are completely artificial. This strategy should substantially facilitate the identification of novel or variant peptides and proteins, and increase the power of MALDI-PSD analyses in proteomics. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:907 / 913
页数:7
相关论文
共 47 条
[1]   Complete sequencing of anti-vancomycin fab fragment by liquid chromatography-electrospray ion trap mass spectrometry with a combination of database searching and manual interpretation of the MS/MS spectra [J].
Adamczyk, M ;
Gebler, JC ;
Wu, J ;
Yu, ZG .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 260 (1-2) :235-249
[2]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[3]   SEQUENCING OF PEPTIDES BY TANDEM MASS-SPECTROMETRY AND HIGH-ENERGY COLLISION-INDUCED DISSOCIATION [J].
BIEMANN, K .
METHODS IN ENZYMOLOGY, 1990, 193 :455-479
[4]   Four decades of structure determination by mass spectrometry: From alkaloids to heparin [J].
Biemann, K .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2002, 13 (11) :1254-1272
[5]   NOMENCLATURE FOR PEPTIDE FRAGMENT IONS (POSITIVE-IONS) [J].
BIEMANN, K .
METHODS IN ENZYMOLOGY, 1990, 193 :886-887
[6]   De novo peptide sequencing and quantitative profiling of complex protein mixtures using mass-coded abundance tagging [J].
Cagney, G ;
Emili, A .
NATURE BIOTECHNOLOGY, 2002, 20 (02) :163-170
[7]   Peptide and protein identification by matrix-assisted laser desorption ionization (MALDI) and MALDI-post-source decay time-of-flight mass spectrometry [J].
Chaurand, P ;
Luetzenkirchen, F ;
Spengler, B .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1999, 10 (02) :91-103
[8]  
Creasy DM, 2002, PROTEOMICS, V2, P1426, DOI 10.1002/1615-9861(200210)2:10<1426::AID-PROT1426>3.0.CO
[9]  
2-5
[10]   Development of new methodologies for the mass spectrometry study of bioorganic macromolecules [J].
Cristoni, S ;
Bernardi, LR .
MASS SPECTROMETRY REVIEWS, 2003, 22 (06) :369-406