ProtQuant: a tool for the label-free quantification of MudPIT proteomics data

被引:34
作者
Bridges, Susan M. [1 ,4 ]
Magee, G. Bryce [1 ,4 ]
Wang, Nan [1 ,4 ]
Williams, W. Paul [3 ,4 ]
Burgess, Shane C. [2 ,4 ,5 ]
Nanduri, Bindu [2 ,4 ]
机构
[1] Mississippi State Univ, Dept Comp Sci & Engn, Starkville, MS 39762 USA
[2] Mississippi State Univ, Coll Vet Med, Starkville, MS 39762 USA
[3] Mississippi State Univ, USDA ARS Corn Host Plant Resistance Res Unit, Starkville, MS 39762 USA
[4] Mississippi State Univ, Inst Digital Biol, Starkville, MS 39762 USA
[5] Mississippi State Univ, Mississippi Agr & Forestry Expt Stn, Starkville, MS 39762 USA
关键词
D O I
10.1186/1471-2105-8-S7-S24
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Effective and economical methods for quantitative analysis of high throughput mass spectrometry data are essential to meet the goals of directly identifying, characterizing, and quantifying proteins from a particular cell state. Multidimensional Protein Identification Technology (MudPIT) is a common approach used in protein identification. Two types of methods are used to detect differential protein expression in MudPIT experiments: those involving stable isotope labelling and the so-called label-free methods. Label-free methods are based on the relationship between protein abundance and sampling statistics such as peptide count, spectral count, probabilistic peptide identification scores, and sum of peptide Sequest XCorr scores (Sigma XCorr). Although a number of label-free methods for protein quantification have been described in the literature, there are few publicly available tools that implement these methods. We describe ProtQuant, a Java-based tool for label-free protein quantification that uses the previously published Sigma XCorr method for quantification and includes an improved method for handling missing data. Results: ProtQuant was designed for ease of use and portability for the bench scientist. It implements the Sigma XCorr method for label free protein quantification from MudPIT datasets. ProtQuant has a graphical user interface, accepts multiple file formats, is not limited by the size of the input files, and can process any number of replicates and any number of treatments. In addition, ProtQuant implements a new method for dealing with missing values for peptide scores used for quantification. The new algorithm, called Sigma XCorr*, uses "below threshold" peptide scores to provide meaningful non-zero values for missing data points. We demonstrate that Sigma XCorr* produces an average reduction in false positive identifications of differential expression of 25% compared to Sigma XCorr. Conclusion: ProtQuant is a tool for protein quantification built for multi-platform use with an intuitive user interface. ProtQuant efficiently and uniquely performs label-free quantification of protein datasets produced with Sequest and provides the user with facilities for data management and analysis. Importantly, ProtQuant is available as a self-installing executable for the Windows environment used by many bench scientists.
引用
收藏
页数:9
相关论文
共 21 条
[1]   Direct proteomic mapping of the lung microvascular endothelial cell surface in vivo and in cell culture [J].
Durr, E ;
Yu, JY ;
Krasinska, KM ;
Carver, LA ;
Yates, JR ;
Testa, JE ;
Oh, P ;
Schnitzer, JE .
NATURE BIOTECHNOLOGY, 2004, 22 (08) :985-992
[2]   Comparative evaluation of mass spectrometry platforms used in large-scale proteomics investigations [J].
Elias, JE ;
Haas, W ;
Faherty, BK ;
Gygi, SP .
NATURE METHODS, 2005, 2 (09) :667-675
[3]   Target-decoy search strategy for increased confidence in large-scale protein identifications by mass spectrometry [J].
Elias, Joshua E. ;
Gygi, Steven P. .
NATURE METHODS, 2007, 4 (03) :207-214
[4]   AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE [J].
ENG, JK ;
MCCORMACK, AL ;
YATES, JR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) :976-989
[5]   A proteomic view of the Plasmodium falciparum life cycle [J].
Florens, L ;
Washburn, MP ;
Raine, JD ;
Anthony, RM ;
Grainger, M ;
Haynes, JD ;
Moch, JK ;
Muster, N ;
Sacci, JB ;
Tabb, DL ;
Witney, AA ;
Wolters, D ;
Wu, YM ;
Gardner, MJ ;
Holder, AA ;
Sinden, RE ;
Yates, JR ;
Carucci, DJ .
NATURE, 2002, 419 (6906) :520-526
[6]   Changes in the protein expression of yeast as a function of carbon source [J].
Gao, J ;
Opiteck, GJ ;
Friedrichs, MS ;
Dongre, AR ;
Hefta, SA .
JOURNAL OF PROTEOME RESEARCH, 2003, 2 (06) :643-649
[7]   Open mass spectrometry search algorithm [J].
Geer, LY ;
Markey, SP ;
Kowalak, JA ;
Wagner, L ;
Xu, M ;
Maynard, DM ;
Yang, XY ;
Shi, WY ;
Bryant, SH .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (05) :958-964
[8]   Quantitative analysis of complex protein mixtures using isotope-coded affinity tags [J].
Gygi, SP ;
Rist, B ;
Gerber, SA ;
Turecek, F ;
Gelb, MH ;
Aebersold, R .
NATURE BIOTECHNOLOGY, 1999, 17 (10) :994-999
[9]   An ensemble approach to microarray data-based gene prioritization after missing value imputation [J].
Hua, Dong ;
Lai, Yinglei .
BIOINFORMATICS, 2007, 23 (06) :747-754
[10]   Exponentially modified protein abundance index (emPAI) for estimation of absolute protein amount in proteomics by the number of sequenced peptides per protein [J].
Ishihama, Y ;
Oda, Y ;
Tabata, T ;
Sato, T ;
Nagasu, T ;
Rappsilber, J ;
Mann, M .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (09) :1265-1272