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Isobaric Matching between Runs and Novel PSM-Level Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification
[Image: see text] Isobaric labeling has the promise of combining high sample multiplexing with precise quantification. However, normalization issues and the missing value problem of complete n-plexes hamper quantification across more than one n-plex. Here, we introduce two novel algorithms implement...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586393/ https://www.ncbi.nlm.nih.gov/pubmed/32892627 http://dx.doi.org/10.1021/acs.jproteome.0c00209 |
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author | Yu, Sung-Huan Kyriakidou, Pelagia Cox, Jürgen |
author_facet | Yu, Sung-Huan Kyriakidou, Pelagia Cox, Jürgen |
author_sort | Yu, Sung-Huan |
collection | PubMed |
description | [Image: see text] Isobaric labeling has the promise of combining high sample multiplexing with precise quantification. However, normalization issues and the missing value problem of complete n-plexes hamper quantification across more than one n-plex. Here, we introduce two novel algorithms implemented in MaxQuant that substantially improve the data analysis with multiple n-plexes. First, isobaric matching between runs makes use of the three-dimensional MS1 features to transfer identifications from identified to unidentified MS/MS spectra between liquid chromatography–mass spectrometry runs in order to utilize reporter ion intensities in unidentified spectra for quantification. On typical datasets, we observe a significant gain in MS/MS spectra that can be used for quantification. Second, we introduce a novel PSM-level normalization, applicable to data with and without the common reference channel. It is a weighted median-based method, in which the weights reflect the number of ions that were used for fragmentation. On a typical dataset, we observe complete removal of batch effects and dominance of the biological sample grouping after normalization. Furthermore, we provide many novel processing and normalization options in Perseus, the companion software for the downstream analysis of quantitative proteomics results. All novel tools and algorithms are available with the regular MaxQuant and Perseus releases, which are downloadable at http://maxquant.org. |
format | Online Article Text |
id | pubmed-7586393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75863932020-10-27 Isobaric Matching between Runs and Novel PSM-Level Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification Yu, Sung-Huan Kyriakidou, Pelagia Cox, Jürgen J Proteome Res [Image: see text] Isobaric labeling has the promise of combining high sample multiplexing with precise quantification. However, normalization issues and the missing value problem of complete n-plexes hamper quantification across more than one n-plex. Here, we introduce two novel algorithms implemented in MaxQuant that substantially improve the data analysis with multiple n-plexes. First, isobaric matching between runs makes use of the three-dimensional MS1 features to transfer identifications from identified to unidentified MS/MS spectra between liquid chromatography–mass spectrometry runs in order to utilize reporter ion intensities in unidentified spectra for quantification. On typical datasets, we observe a significant gain in MS/MS spectra that can be used for quantification. Second, we introduce a novel PSM-level normalization, applicable to data with and without the common reference channel. It is a weighted median-based method, in which the weights reflect the number of ions that were used for fragmentation. On a typical dataset, we observe complete removal of batch effects and dominance of the biological sample grouping after normalization. Furthermore, we provide many novel processing and normalization options in Perseus, the companion software for the downstream analysis of quantitative proteomics results. All novel tools and algorithms are available with the regular MaxQuant and Perseus releases, which are downloadable at http://maxquant.org. American Chemical Society 2020-09-07 2020-10-02 /pmc/articles/PMC7586393/ /pubmed/32892627 http://dx.doi.org/10.1021/acs.jproteome.0c00209 Text en This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Yu, Sung-Huan Kyriakidou, Pelagia Cox, Jürgen Isobaric Matching between Runs and Novel PSM-Level Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification |
title | Isobaric Matching
between Runs and Novel PSM-Level
Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification |
title_full | Isobaric Matching
between Runs and Novel PSM-Level
Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification |
title_fullStr | Isobaric Matching
between Runs and Novel PSM-Level
Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification |
title_full_unstemmed | Isobaric Matching
between Runs and Novel PSM-Level
Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification |
title_short | Isobaric Matching
between Runs and Novel PSM-Level
Normalization in MaxQuant Strongly Improve Reporter Ion-Based Quantification |
title_sort | isobaric matching
between runs and novel psm-level
normalization in maxquant strongly improve reporter ion-based quantification |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586393/ https://www.ncbi.nlm.nih.gov/pubmed/32892627 http://dx.doi.org/10.1021/acs.jproteome.0c00209 |
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