Application of Peptide LC Retention Time Information in a Discriminant Function for Peptide Identification by Tandem Mass Spectrometry

We describe the application of a peptide retention time reversed phase liquid chromatography (RPLC) prediction model previously reported (Petritis et al. Anal. Chem. 2003, 75, 1039) for improved peptide identification. The model uses peptide sequence information to generate a theoretical (predicted)...

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Veröffentlicht in:Journal of Proteome Research, 3(4):760-769 3(4):760-769, 2004-07, Vol.3 (4), p.760-769
Hauptverfasser: Strittmatter, Eric F, Kangas, Lars J, Petritis, Konstantinos, Mottaz, Heather M, Anderson, Gordon A, Shen, Yufeng, Jacobs, Jon M, Camp, David G, Smith, Richard D
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container_issue 4
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container_title Journal of Proteome Research, 3(4):760-769
container_volume 3
creator Strittmatter, Eric F
Kangas, Lars J
Petritis, Konstantinos
Mottaz, Heather M
Anderson, Gordon A
Shen, Yufeng
Jacobs, Jon M
Camp, David G
Smith, Richard D
description We describe the application of a peptide retention time reversed phase liquid chromatography (RPLC) prediction model previously reported (Petritis et al. Anal. Chem. 2003, 75, 1039) for improved peptide identification. The model uses peptide sequence information to generate a theoretical (predicted) elution time that can be compared with the observed elution time. Using data from a set of known proteins, the retention time parameter was incorporated into a discriminant function for use with tandem mass spectrometry (MS/MS) data analyzed with the peptide/protein identification program SEQUEST. For singly charged ions, the number of confident identifications increased by 12% when the elution time metric is included compared to when mass spectral data is the sole source of information in the context of a Drosophila melanogaster database. A 3−4% improvement was obtained for doubly and triply charged ions for the same biological system. Application to the larger Rattus norvegicus (rat) and human proteome databases resulted in an 8−9% overall increase in the number of confident identifications, when both the discriminant function and elution time are used. The effect of adding “runner-up” hits (peptide matches that are not the highest scoring for a spectra) from SEQUEST is also explored, and we find that the number of confident identifications is further increased by 1% when these hits are also considered. Finally, application of the discriminant functions derived in this work with ∼2.2 million spectra from over three hundred LC−MS/MS analyses of peptides from human plasma protein resulted in a 16% increase in confident peptide identifications (9022 vs 7779) using elution time information. Further improvements from the use of elution time information can be expected as both the experimental control of elution time reproducibility and the predictive capability are improved. Keywords: bioinformatics • proteome • algorithm • accurate mass and time tag • multivariate statistics • capillary liquid-chromatography • retention time • FTICR
doi_str_mv 10.1021/pr049965y
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A 3−4% improvement was obtained for doubly and triply charged ions for the same biological system. Application to the larger Rattus norvegicus (rat) and human proteome databases resulted in an 8−9% overall increase in the number of confident identifications, when both the discriminant function and elution time are used. The effect of adding “runner-up” hits (peptide matches that are not the highest scoring for a spectra) from SEQUEST is also explored, and we find that the number of confident identifications is further increased by 1% when these hits are also considered. Finally, application of the discriminant functions derived in this work with ∼2.2 million spectra from over three hundred LC−MS/MS analyses of peptides from human plasma protein resulted in a 16% increase in confident peptide identifications (9022 vs 7779) using elution time information. Further improvements from the use of elution time information can be expected as both the experimental control of elution time reproducibility and the predictive capability are improved. 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(PNNL), Richland, WA (United States)</creatorcontrib><title>Application of Peptide LC Retention Time Information in a Discriminant Function for Peptide Identification by Tandem Mass Spectrometry</title><title>Journal of Proteome Research, 3(4):760-769</title><addtitle>J. Proteome Res</addtitle><description>We describe the application of a peptide retention time reversed phase liquid chromatography (RPLC) prediction model previously reported (Petritis et al. Anal. Chem. 2003, 75, 1039) for improved peptide identification. The model uses peptide sequence information to generate a theoretical (predicted) elution time that can be compared with the observed elution time. Using data from a set of known proteins, the retention time parameter was incorporated into a discriminant function for use with tandem mass spectrometry (MS/MS) data analyzed with the peptide/protein identification program SEQUEST. For singly charged ions, the number of confident identifications increased by 12% when the elution time metric is included compared to when mass spectral data is the sole source of information in the context of a Drosophila melanogaster database. A 3−4% improvement was obtained for doubly and triply charged ions for the same biological system. Application to the larger Rattus norvegicus (rat) and human proteome databases resulted in an 8−9% overall increase in the number of confident identifications, when both the discriminant function and elution time are used. The effect of adding “runner-up” hits (peptide matches that are not the highest scoring for a spectra) from SEQUEST is also explored, and we find that the number of confident identifications is further increased by 1% when these hits are also considered. Finally, application of the discriminant functions derived in this work with ∼2.2 million spectra from over three hundred LC−MS/MS analyses of peptides from human plasma protein resulted in a 16% increase in confident peptide identifications (9022 vs 7779) using elution time information. Further improvements from the use of elution time information can be expected as both the experimental control of elution time reproducibility and the predictive capability are improved. 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The effect of adding “runner-up” hits (peptide matches that are not the highest scoring for a spectra) from SEQUEST is also explored, and we find that the number of confident identifications is further increased by 1% when these hits are also considered. Finally, application of the discriminant functions derived in this work with ∼2.2 million spectra from over three hundred LC−MS/MS analyses of peptides from human plasma protein resulted in a 16% increase in confident peptide identifications (9022 vs 7779) using elution time information. Further improvements from the use of elution time information can be expected as both the experimental control of elution time reproducibility and the predictive capability are improved. 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source MEDLINE; ACS Journals: American Chemical Society Web Editions
subjects Animals
BASIC BIOLOGICAL SCIENCES
CHROMATOGRAPHY
Chromatography, Liquid
DROSOPHILA
Drosophila Proteins - chemistry
FORECASTING
Mass Spectrometry
MASS SPECTROSCOPY
METRICS
PEPTIDES
Peptides - analysis
Peptides - chemistry
Peptides - isolation & purification
PLASMA
PROTEINS
Proteome - chemistry
Rats
RETENTION
Software
SPECTRA
title Application of Peptide LC Retention Time Information in a Discriminant Function for Peptide Identification by Tandem Mass Spectrometry
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