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Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry

Quantitative proteomics employing mass spectrometry is an indispensable tool in life science research. Targeted proteomics has emerged as a powerful approach for reproducible quantification but is limited in the number of proteins quantified. SWATH-mass spectrometry consists of data-independent acqu...

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Autores principales: Collins, Ben C., Hunter, Christie L., Liu, Yansheng, Schilling, Birgit, Rosenberger, George, Bader, Samuel L., Chan, Daniel W., Gibson, Bradford W., Gingras, Anne-Claude, Held, Jason M., Hirayama-Kurogi, Mio, Hou, Guixue, Krisp, Christoph, Larsen, Brett, Lin, Liang, Liu, Siqi, Molloy, Mark P., Moritz, Robert L., Ohtsuki, Sumio, Schlapbach, Ralph, Selevsek, Nathalie, Thomas, Stefani N., Tzeng, Shin-Cheng, Zhang, Hui, Aebersold, Ruedi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566333/
https://www.ncbi.nlm.nih.gov/pubmed/28827567
http://dx.doi.org/10.1038/s41467-017-00249-5
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author Collins, Ben C.
Hunter, Christie L.
Liu, Yansheng
Schilling, Birgit
Rosenberger, George
Bader, Samuel L.
Chan, Daniel W.
Gibson, Bradford W.
Gingras, Anne-Claude
Held, Jason M.
Hirayama-Kurogi, Mio
Hou, Guixue
Krisp, Christoph
Larsen, Brett
Lin, Liang
Liu, Siqi
Molloy, Mark P.
Moritz, Robert L.
Ohtsuki, Sumio
Schlapbach, Ralph
Selevsek, Nathalie
Thomas, Stefani N.
Tzeng, Shin-Cheng
Zhang, Hui
Aebersold, Ruedi
author_facet Collins, Ben C.
Hunter, Christie L.
Liu, Yansheng
Schilling, Birgit
Rosenberger, George
Bader, Samuel L.
Chan, Daniel W.
Gibson, Bradford W.
Gingras, Anne-Claude
Held, Jason M.
Hirayama-Kurogi, Mio
Hou, Guixue
Krisp, Christoph
Larsen, Brett
Lin, Liang
Liu, Siqi
Molloy, Mark P.
Moritz, Robert L.
Ohtsuki, Sumio
Schlapbach, Ralph
Selevsek, Nathalie
Thomas, Stefani N.
Tzeng, Shin-Cheng
Zhang, Hui
Aebersold, Ruedi
author_sort Collins, Ben C.
collection PubMed
description Quantitative proteomics employing mass spectrometry is an indispensable tool in life science research. Targeted proteomics has emerged as a powerful approach for reproducible quantification but is limited in the number of proteins quantified. SWATH-mass spectrometry consists of data-independent acquisition and a targeted data analysis strategy that aims to maintain the favorable quantitative characteristics (accuracy, sensitivity, and selectivity) of targeted proteomics at large scale. While previous SWATH-mass spectrometry studies have shown high intra-lab reproducibility, this has not been evaluated between labs. In this multi-laboratory evaluation study including 11 sites worldwide, we demonstrate that using SWATH-mass spectrometry data acquisition we can consistently detect and reproducibly quantify >4000 proteins from HEK293 cells. Using synthetic peptide dilution series, we show that the sensitivity, dynamic range and reproducibility established with SWATH-mass spectrometry are uniformly achieved. This study demonstrates that the acquisition of reproducible quantitative proteomics data by multiple labs is achievable, and broadly serves to increase confidence in SWATH-mass spectrometry data acquisition as a reproducible method for large-scale protein quantification.
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spelling pubmed-55663332017-08-29 Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry Collins, Ben C. Hunter, Christie L. Liu, Yansheng Schilling, Birgit Rosenberger, George Bader, Samuel L. Chan, Daniel W. Gibson, Bradford W. Gingras, Anne-Claude Held, Jason M. Hirayama-Kurogi, Mio Hou, Guixue Krisp, Christoph Larsen, Brett Lin, Liang Liu, Siqi Molloy, Mark P. Moritz, Robert L. Ohtsuki, Sumio Schlapbach, Ralph Selevsek, Nathalie Thomas, Stefani N. Tzeng, Shin-Cheng Zhang, Hui Aebersold, Ruedi Nat Commun Article Quantitative proteomics employing mass spectrometry is an indispensable tool in life science research. Targeted proteomics has emerged as a powerful approach for reproducible quantification but is limited in the number of proteins quantified. SWATH-mass spectrometry consists of data-independent acquisition and a targeted data analysis strategy that aims to maintain the favorable quantitative characteristics (accuracy, sensitivity, and selectivity) of targeted proteomics at large scale. While previous SWATH-mass spectrometry studies have shown high intra-lab reproducibility, this has not been evaluated between labs. In this multi-laboratory evaluation study including 11 sites worldwide, we demonstrate that using SWATH-mass spectrometry data acquisition we can consistently detect and reproducibly quantify >4000 proteins from HEK293 cells. Using synthetic peptide dilution series, we show that the sensitivity, dynamic range and reproducibility established with SWATH-mass spectrometry are uniformly achieved. This study demonstrates that the acquisition of reproducible quantitative proteomics data by multiple labs is achievable, and broadly serves to increase confidence in SWATH-mass spectrometry data acquisition as a reproducible method for large-scale protein quantification. Nature Publishing Group UK 2017-08-21 /pmc/articles/PMC5566333/ /pubmed/28827567 http://dx.doi.org/10.1038/s41467-017-00249-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Collins, Ben C.
Hunter, Christie L.
Liu, Yansheng
Schilling, Birgit
Rosenberger, George
Bader, Samuel L.
Chan, Daniel W.
Gibson, Bradford W.
Gingras, Anne-Claude
Held, Jason M.
Hirayama-Kurogi, Mio
Hou, Guixue
Krisp, Christoph
Larsen, Brett
Lin, Liang
Liu, Siqi
Molloy, Mark P.
Moritz, Robert L.
Ohtsuki, Sumio
Schlapbach, Ralph
Selevsek, Nathalie
Thomas, Stefani N.
Tzeng, Shin-Cheng
Zhang, Hui
Aebersold, Ruedi
Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry
title Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry
title_full Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry
title_fullStr Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry
title_full_unstemmed Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry
title_short Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry
title_sort multi-laboratory assessment of reproducibility, qualitative and quantitative performance of swath-mass spectrometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566333/
https://www.ncbi.nlm.nih.gov/pubmed/28827567
http://dx.doi.org/10.1038/s41467-017-00249-5
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