Post Analysis Data Acquisition for the Iterative MS/MS Sampling of Proteomics Mixtures

被引:48
作者
Hoopmann, Michael R. [1 ]
Merrihew, Gennifer E. [1 ]
von Haller, Priska D. [1 ]
MacCoss, Michael J. [1 ]
机构
[1] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
instrument control; technical replicates; high resolution; isotope distributions; Fourier transform mass spectrometry; AMINO-ACID-SEQUENCES; TANDEM MASS-SPECTRA; PROTEIN IDENTIFICATION; PEPTIDE IDENTIFICATION; QUANTITATIVE-ANALYSIS; COMPLEX PEPTIDE; ION-TRAP; SPECTROMETRY;
D O I
10.1021/pr800828p
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The identification of peptides by microcapillary liquid chromatography-tandem mass spectrometry (mu LC-MS/MS) has become routine because of the development of fast scanning mass spectrometers, data-dependent acquisition, and database searching algorithms. However, many peptides within the detection limit of the mass spectrometer remain unidentified because of limitations in MS/MS sampling speed despite the dynamic range and peak capacity of the instrument. We have developed an automated approach that uses the mass spectra from high resolution mu LC-MS data to define the molecular species present in the mixture and directs the acquisition of MS/MS spectra to precursors that were missed in prior analyses. This approach increases the coverage of the molecular species sampled by MS/MS and consequently the number of peptides and proteins identified during the acquisition of technical or biological replicates using a simple one-dimensional chromatographic separation. The combination of a unique workflow and custom software contribute to the improved identification of molecular features detected in proteomics experiments of complex protein mixtures.
引用
收藏
页码:1870 / 1875
页数:6
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