Literature DB >> 15772112

Improving protein identification using complementary fragmentation techniques in fourier transform mass spectrometry.

Michael L Nielsen1, Mikhail M Savitski, Roman A Zubarev.   

Abstract

Identification of proteins by MS/MS is performed by matching experimental mass spectra against calculated spectra of all possible peptides in a protein data base. The search engine assigns each spectrum a score indicating how well the experimental data complies with the expected one; a higher score means increased confidence in the identification. One problem is the false-positive identifications, which arise from incomplete data as well as from the presence of misleading ions in experimental mass spectra due to gas-phase reactions, stray ions, contaminants, and electronic noise. We employed a novel technique of reduction of false positives that is based on a combined use of orthogonal fragmentation techniques electron capture dissociation (ECD) and collisionally activated dissociation (CAD). Since ECD and CAD exhibit many complementary properties, their combined use greatly increased the analysis specificity, which was further strengthened by the high mass accuracy (approximately 1 ppm) afforded by Fourier transform mass spectrometry. The utility of this approach is demonstrated on a whole cell lysate from Escherichia coli. Analysis was made using the data-dependent acquisition mode. Extraction of complementary sequence information was performed prior to data base search using in-house written software. Only masses involved in complementary pairs in the MS/MS spectrum from the same or orthogonal fragmentation techniques were submitted to the data base search. ECD/CAD identified twice as many proteins at a fixed statistically significant confidence level with on average a 64% higher Mascot score. The confidence in protein identification was hereby increased by more than 1 order of magnitude. The combined ECD/CAD searches were on average 20% faster than CAD-only searches. A specially developed test with scrambled MS/MS data revealed that the amount of false-positive identifications was dramatically reduced by the combined use of CAD and ECD.

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Year:  2005        PMID: 15772112     DOI: 10.1074/mcp.T400022-MCP200

Source DB:  PubMed          Journal:  Mol Cell Proteomics        ISSN: 1535-9476            Impact factor:   5.911


  48 in total

1.  Effects of peptide backbone amide-to-ester bond substitution on the cleavage frequency in electron capture dissociation and collision-activated dissociation.

Authors:  Frank Kjeldsen; Roman A Zubarev
Journal:  J Am Soc Mass Spectrom       Date:  2011-05-05       Impact factor: 3.109

2.  The generating function of CID, ETD, and CID/ETD pairs of tandem mass spectra: applications to database search.

Authors:  Sangtae Kim; Nikolai Mischerikow; Nuno Bandeira; J Daniel Navarro; Louis Wich; Shabaz Mohammed; Albert J R Heck; Pavel A Pevzner
Journal:  Mol Cell Proteomics       Date:  2010-09-09       Impact factor: 5.911

3.  The relative charge ratio between C and N atoms in amide bond acts as a key factor to determine peptide fragment efficiency in different charge states.

Authors:  Feng Sun; Wansong Zong; Rutao Liu; Meijie Wang; Pengjun Zhang; Qifei Xu
Journal:  J Am Soc Mass Spectrom       Date:  2010-07-08       Impact factor: 3.109

4.  Thermal proteome profiling for unbiased identification of direct and indirect drug targets using multiplexed quantitative mass spectrometry.

Authors:  Holger Franken; Toby Mathieson; Dorothee Childs; Gavain M A Sweetman; Thilo Werner; Ina Tögel; Carola Doce; Stephan Gade; Marcus Bantscheff; Gerard Drewes; Friedrich B M Reinhard; Wolfgang Huber; Mikhail M Savitski
Journal:  Nat Protoc       Date:  2015-09-17       Impact factor: 13.491

Review 5.  Accurate mass measurements in proteomics.

Authors:  Tao Liu; Mikhail E Belov; Navdeep Jaitly; Wei-Jun Qian; Richard D Smith
Journal:  Chem Rev       Date:  2007-07-25       Impact factor: 60.622

6.  Evidence for sequence scrambling in collision-induced dissociation of y-type fragment ions.

Authors:  Mahsan Miladi; Brett Harper; Touradj Solouki
Journal:  J Am Soc Mass Spectrom       Date:  2013-08-28       Impact factor: 3.109

7.  On performing simultaneous electron transfer dissociation and collision-induced dissociation on multiply protonated peptides in a linear ion trap.

Authors:  J Larry Campbell; James W Hager; J C Yves Le Blanc
Journal:  J Am Soc Mass Spectrom       Date:  2009-05-20       Impact factor: 3.109

8.  Bifurcating fragmentation behavior of gas-phase tryptic peptide dications in collisional activation.

Authors:  Mikhail M Savitski; Maria Fälth; Y M Eva Fung; Christopher M Adams; Roman A Zubarev
Journal:  J Am Soc Mass Spectrom       Date:  2008-08-09       Impact factor: 3.109

9.  Characterization of 4-hydroxy-2-nonenal-modified peptides by liquid chromatography-tandem mass spectrometry using data-dependent acquisition: neutral loss-driven MS3 versus neutral loss-driven electron capture dissociation.

Authors:  Navin Rauniyar; Stanley M Stevens; Katalin Prokai-Tatrai; Laszlo Prokai
Journal:  Anal Chem       Date:  2009-01-15       Impact factor: 6.986

10.  Systematic characterization of high mass accuracy influence on false discovery and probability scoring in peptide mass fingerprinting.

Authors:  Eric D Dodds; Brian H Clowers; Paul J Hagerman; Carlito B Lebrilla
Journal:  Anal Biochem       Date:  2007-10-11       Impact factor: 3.365

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