Prophossi: automating expert validation of phosphopeptide-spectrum matches from tandem mass spectrometry

被引:13
作者
Martin, David M. A. [1 ]
Nett, Isabelle R. E. [1 ]
Vandermoere, Franck [2 ]
Barber, Jonathan D. [1 ]
Morrice, Nicholas A. [2 ]
Ferguson, Michael A. J. [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Div Biol Chem & Drug Discovery, Dundee DD1 5EH, Scotland
[2] Univ Dundee, Coll Life Sci, MRC Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
PHOSPHORYLATED PROTEINS; AFFINITY-CHROMATOGRAPHY; TRYPANOSOMA-BRUCEI; IDENTIFICATION; PHOSPHOPROTEINS; LOCALIZATION; NETWORKS; DATABASE;
D O I
10.1093/bioinformatics/btq341
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Complex patterns of protein phosphorylation mediate many cellular processes. Tandem mass spectrometry (MS/MS) is a powerful tool for identifying these post-translational modifications. In high-throughput experiments, mass spectrometry database search engines, such as MASCOT provide a ranked list of peptide identifications based on hundreds of thousands of MS/MS spectra obtained in a mass spectrometry experiment. These search results are not in themselves sufficient for confident assignment of phosphorylation sites as identification of characteristic mass differences requires time-consuming manual assessment of the spectra by an experienced analyst. The time required for manual assessment has previously rendered high-throughput confident assignment of phosphorylation sites challenging. Results: We have developed a knowledge base of criteria, which replicate expert assessment, allowing more than half of cases to be automatically validated and site assignments verified with a high degree of confidence. This was assessed by comparing automated spectral interpretation with careful manual examination of the assignments for 501 peptides above the 1% false discovery rate (FOR) threshold corresponding to 259 putative phosphorylation sites in 74 proteins of the Trypanosoma brucei proteome. Despite this stringent approach, we are able to validate 80 of the 91 phosphorylation sites (88%) positively identified by manual examination of the spectra used for the MASCOT searches with a FOR < 15%. Conclusions: High-throughput computational analysis can provide a viable second stage validation of primary mass spectrometry database search results. Such validation gives rapid access to a systems level overview of protein phosphorylation in the experiment under investigation.
引用
收藏
页码:2153 / 2159
页数:7
相关论文
共 23 条
[1]   ISOLATION OF PHOSPHOPROTEINS BY IMMOBILIZED METAL (FE-3+) AFFINITY-CHROMATOGRAPHY [J].
ANDERSSON, L ;
PORATH, J .
ANALYTICAL BIOCHEMISTRY, 1986, 154 (01) :250-254
[2]   A probability-based approach for high-throughput protein phosphorylation analysis and site localization [J].
Beausoleil, Sean A. ;
Villen, Judit ;
Gerber, Scott A. ;
Rush, John ;
Gygi, Steven P. .
NATURE BIOTECHNOLOGY, 2006, 24 (10) :1285-1292
[3]   Cleavage N-terminal to proline: Analysis of a database of peptide tandem mass spectra [J].
Breci, LA ;
Tabb, DL ;
Yates, JR ;
Wysocki, VH .
ANALYTICAL CHEMISTRY, 2003, 75 (09) :1963-1971
[5]   Is proteomics the new genomics? [J].
Cox, Juergen ;
Mann, Matthias .
CELL, 2007, 130 (03) :395-398
[6]   Intensity-based protein identification by machine learning from a library of tandem mass spectra [J].
Elias, JE ;
Gibbons, FD ;
King, OD ;
Roth, FP ;
Gygi, SP .
NATURE BIOTECHNOLOGY, 2004, 22 (02) :214-219
[7]   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
[8]   A mass spectrometry-based proteomic approach for identification of serine/threonine-phosphorylated proteins by enrichment with phospho-specific antibodies - Identification of a novel protein, Frigg, as a protein kinase A substrate [J].
Gronborg, M ;
Kristiansen, TZ ;
Stensballe, A ;
Andersen, JS ;
Ohara, O ;
Mann, M ;
Jensen, ON ;
Pandey, A .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (07) :517-527
[9]   Phosphoproteomics toolbox: Computational biology, protein chemistry and mass spectrometry [J].
Hjerrild, Majbrit ;
Gammeltoft, Steen .
FEBS LETTERS, 2006, 580 (20) :4764-4770
[10]   Posterior error probabilities and false discovery rates:: Two sides of the same coin [J].
Kaell, Lukas ;
Storey, John D. ;
MacCoss, Michael J. ;
Noble, William Stafford .
JOURNAL OF PROTEOME RESEARCH, 2008, 7 (01) :40-44