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      Enhanced Peptide Identification by Electron Transfer Dissociation Using an Improved Mascot Percolator*

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          Abstract

          Peptide identification using tandem mass spectrometry is a core technology in proteomics. Latest generations of mass spectrometry instruments enable the use of electron transfer dissociation (ETD) to complement collision induced dissociation (CID) for peptide fragmentation. However, a critical limitation to the use of ETD has been optimal database search software. Percolator is a post-search algorithm, which uses semi-supervised machine learning to improve the rate of peptide spectrum identifications (PSMs) together with providing reliable significance measures. We have previously interfaced the Mascot search engine with Percolator and demonstrated sensitivity and specificity benefits with CID data. Here, we report recent developments in the Mascot Percolator V2.0 software including an improved feature calculator and support for a wider range of ion series. The updated software is applied to the analysis of several CID and ETD fragmented peptide data sets. This version of Mascot Percolator increases the number of CID PSMs by up to 80% and ETD PSMs by up to 60% at a 0.01 q-value (1% false discovery rate) threshold over a standard Mascot search, notably recovering PSMs from high charge state precursor ions. The greatly increased number of PSMs and peptide coverage afforded by Mascot Percolator has enabled a fuller assessment of CID/ETD complementarity to be performed. Using a data set of CID and ETcaD spectral pairs, we find that at a 1% false discovery rate, the overlap in peptide identifications by CID and ETD is 83%, which is significantly higher than that obtained using either stand-alone Mascot (69%) or OMSSA (39%). We conclude that Mascot Percolator is a highly sensitive and accurate post-search algorithm for peptide identification and allows direct comparison of peptide identifications using multiple alternative fragmentation techniques.

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          Most cited references32

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          TANDEM: matching proteins with tandem mass spectra.

          Tandem mass spectra obtained from fragmenting peptide ions contain some peptide sequence specific information, but often there is not enough information to sequence the original peptide completely. Several proprietary software applications have been developed to attempt to match the spectra with a list of protein sequences that may contain the sequence of the peptide. The application TANDEM was written to provide the proteomics research community with a set of components that can be used to test new methods and algorithms for performing this type of sequence-to-data matching. The source code and binaries for this software are available at http://www.proteome.ca/opensource.html, for Windows, Linux and Macintosh OSX. The source code is made available under the Artistic License, from the authors.
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            Peptide and protein sequence analysis by electron transfer dissociation mass spectrometry.

            Peptide sequence analysis using a combination of gas-phase ion/ion chemistry and tandem mass spectrometry (MS/MS) is demonstrated. Singly charged anthracene anions transfer an electron to multiply protonated peptides in a radio frequency quadrupole linear ion trap (QLT) and induce fragmentation of the peptide backbone along pathways that are analogous to those observed in electron capture dissociation. Modifications to the QLT that enable this ion/ion chemistry are presented, and automated acquisition of high-quality, single-scan electron transfer dissociation MS/MS spectra of phosphopeptides separated by nanoflow HPLC is described.
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              Open mass spectrometry search algorithm.

              Large numbers of MS/MS peptide spectra generated in proteomics experiments require efficient, sensitive and specific algorithms for peptide identification. In the Open Mass Spectrometry Search Algorithm (OMSSA), specificity is calculated by a classic probability score using an explicit model for matching experimental spectra to sequences. At default thresholds, OMSSA matches more spectra from a standard protein cocktail than a comparable algorithm. OMSSA is designed to be faster than published algorithms in searching large MS/MS datasets.
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                Author and article information

                Journal
                Mol Cell Proteomics
                Mol. Cell Proteomics
                mcprot
                mcprot
                MCP
                Molecular & Cellular Proteomics : MCP
                The American Society for Biochemistry and Molecular Biology
                1535-9476
                1535-9484
                August 2012
                6 April 2012
                6 April 2012
                : 11
                : 8
                : 478-491
                Affiliations
                [1]From the ‡Proteomic Mass Spectrometry, Wellcome Trust Sanger Institute, Hinxton, Cambridge, CB10 1SA;
                [2]§Science for Life Laboratory, School of Biotechnology, Royal Institute of Technology (KTH), Solna, Sweden
                Author notes
                ¶ To whom correspondence should be addressed: Proteomic Mass Spectrometry, Wellcome Trust Sanger Institute, Genome Campus, Hinxton, Cambridge, CB10 1SA. Tel.: +44 (0)1223 834244; E-mail: jc4@ 123456sanger.ac.uk .
                Article
                O111.014522
                10.1074/mcp.O111.014522
                3412976
                22493177
                dc647e4e-4e43-475f-9e2b-cb9fdd9a6652
                © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.

                Creative Commons Attribution Non-Commercial License applies to Author Choice Articles

                History
                : 19 September 2011
                : 27 February 2012
                Categories
                Technological Innovation and Resources

                Molecular biology
                Molecular biology

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