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Integrated Post-Experiment Monoisotopic Mass Refinement: An Integrated Approach to Accurately Assign Monoisotopic Precursor Masses to Tandem Mass Spectrometric Data

Authors
Jung, Hee-JungPurvine, Samuel O.Kim, HokeunPetyuk, Vladislav A.Hyung, Seok-WonMonroe, Matthew E.Mun, Dong-GiKim, Kyong-ChulPark, Jong-MoonKim, Su-JinTolic, NikolaSlysz, Gordon W.Moore, Ronald J.Zhao, RuiAdkins, Joshua N.Anderson, Gordon A.Lee, HookeunCamp, David G., IIYu, Myeong-HeeSmith, Richard D.Lee, Sang-Won
Issue Date
15-10월-2010
Publisher
AMER CHEMICAL SOC
Citation
ANALYTICAL CHEMISTRY, v.82, no.20, pp.8510 - 8518
Indexed
SCIE
SCOPUS
Journal Title
ANALYTICAL CHEMISTRY
Volume
82
Number
20
Start Page
8510
End Page
8518
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/115514
DOI
10.1021/ac101388b
ISSN
0003-2700
Abstract
Accurate assignment of monoisotopic precursor masses to tandem mass spectrometric (MS/MS) data is a fundamental and critically important step for successful peptide identifications in mass spectrometry based proteomics. Here we describe an integrated approach that combines three previously reported methods of treating MS/MS data for precursor mass refinement. This combined method, "integrated post-experiment monoisotopic mass refinement" (iPE-MMR), integrates steps (1) generation of refined MS/MS data by DeconMSn; (2) additional refinement of the resultant MS/MS data by a modified version of PE-MMR; and (3) elimination of systematic errors of precursor masses using DtaRefinery. iPE-MMR is the first method that utilizes all MS information from multiple MS scans of a precursor ion including multiple charge states, in an MS scan, to determine precursor mass. With the combination of these methods, iPE-MMR increases sensitivity in peptide identification and provides increased accuracy when applied to complex high-throughput proteomics data.
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