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Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations

Recent improvements in the mass accuracy and resolution of mass spectrometers have led to renewed interest in label-free quantification using data from the primary mass spectrum (MS1) acquired from data-dependent proteomics experiments. The capacity for higher specificity quantification of peptides...

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Autores principales: Higgs, Richard E., Butler, Jon P., Han, Bomie, Knierman, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655581/
https://www.ncbi.nlm.nih.gov/pubmed/23710359
http://dx.doi.org/10.1155/2013/674282
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author Higgs, Richard E.
Butler, Jon P.
Han, Bomie
Knierman, Michael D.
author_facet Higgs, Richard E.
Butler, Jon P.
Han, Bomie
Knierman, Michael D.
author_sort Higgs, Richard E.
collection PubMed
description Recent improvements in the mass accuracy and resolution of mass spectrometers have led to renewed interest in label-free quantification using data from the primary mass spectrum (MS1) acquired from data-dependent proteomics experiments. The capacity for higher specificity quantification of peptides from samples enriched for proteins of biological interest offers distinct advantages for hypothesis generating experiments relative to immunoassay detection methods or prespecified peptide ions measured by multiple reaction monitoring (MRM) approaches. Here we describe an evaluation of different methods to post-process peptide level quantification information to support protein level inference. We characterize the methods by examining their ability to recover a known dilution of a standard protein in background matrices of varying complexity. Additionally, the MS1 quantification results are compared to a standard, targeted, MRM approach on the same samples under equivalent instrument conditions. We show the existence of multiple peptides with MS1 quantification sensitivity similar to the best MRM peptides for each of the background matrices studied. Based on these results we provide recommendations on preferred approaches to leveraging quantitative measurements of multiple peptides to improve protein level inference.
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spelling pubmed-36555812013-05-24 Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations Higgs, Richard E. Butler, Jon P. Han, Bomie Knierman, Michael D. Int J Proteomics Research Article Recent improvements in the mass accuracy and resolution of mass spectrometers have led to renewed interest in label-free quantification using data from the primary mass spectrum (MS1) acquired from data-dependent proteomics experiments. The capacity for higher specificity quantification of peptides from samples enriched for proteins of biological interest offers distinct advantages for hypothesis generating experiments relative to immunoassay detection methods or prespecified peptide ions measured by multiple reaction monitoring (MRM) approaches. Here we describe an evaluation of different methods to post-process peptide level quantification information to support protein level inference. We characterize the methods by examining their ability to recover a known dilution of a standard protein in background matrices of varying complexity. Additionally, the MS1 quantification results are compared to a standard, targeted, MRM approach on the same samples under equivalent instrument conditions. We show the existence of multiple peptides with MS1 quantification sensitivity similar to the best MRM peptides for each of the background matrices studied. Based on these results we provide recommendations on preferred approaches to leveraging quantitative measurements of multiple peptides to improve protein level inference. Hindawi Publishing Corporation 2013 2013-04-23 /pmc/articles/PMC3655581/ /pubmed/23710359 http://dx.doi.org/10.1155/2013/674282 Text en Copyright © 2013 Richard E. Higgs et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Higgs, Richard E.
Butler, Jon P.
Han, Bomie
Knierman, Michael D.
Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations
title Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations
title_full Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations
title_fullStr Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations
title_full_unstemmed Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations
title_short Quantitative Proteomics via High Resolution MS Quantification: Capabilities and Limitations
title_sort quantitative proteomics via high resolution ms quantification: capabilities and limitations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655581/
https://www.ncbi.nlm.nih.gov/pubmed/23710359
http://dx.doi.org/10.1155/2013/674282
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