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PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios

BACKGROUND: Recent development of novel technologies paved the way for quantitative proteomics. One of the most important among them is iTRAQ, employing isobaric tags for relative or absolute quantitation. Despite large progress in technology development, still many challenges remain for derivation...

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Autores principales: Bauer, Chris, Kleinjung, Frank, Rutishauser, Dorothea, Panse, Christian, Chadt, Alexandra, Dreja, Tanja, Al-Hasani, Hadi, Reinert, Knut, Schlapbach, Ralph, Schuchhardt, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368728/
https://www.ncbi.nlm.nih.gov/pubmed/22340093
http://dx.doi.org/10.1186/1471-2105-13-34
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author Bauer, Chris
Kleinjung, Frank
Rutishauser, Dorothea
Panse, Christian
Chadt, Alexandra
Dreja, Tanja
Al-Hasani, Hadi
Reinert, Knut
Schlapbach, Ralph
Schuchhardt, Johannes
author_facet Bauer, Chris
Kleinjung, Frank
Rutishauser, Dorothea
Panse, Christian
Chadt, Alexandra
Dreja, Tanja
Al-Hasani, Hadi
Reinert, Knut
Schlapbach, Ralph
Schuchhardt, Johannes
author_sort Bauer, Chris
collection PubMed
description BACKGROUND: Recent development of novel technologies paved the way for quantitative proteomics. One of the most important among them is iTRAQ, employing isobaric tags for relative or absolute quantitation. Despite large progress in technology development, still many challenges remain for derivation and interpretation of quantitative results. One of these challenges is the consistent assignment of peptides to proteins. RESULTS: We have developed Peptide Profiling Guided Identification of Proteins (PPINGUIN), a statistical analysis workflow for iTRAQ data addressing the problem of ambiguous peptide quantitations. Motivated by the assumption that peptides uniquely derived from the same protein are correlated, our method employs clustering as a very early step in data processing prior to protein inference. Our method increases experimental reproducibility and decreases variability of quantitations of peptides assigned to the same protein. Giving further support to our method, application to a type 2 diabetes dataset identifies a list of protein candidates that is in very good agreement with previously performed transcriptomics meta analysis. Making use of quantitative properties of signal patterns identified, PPINGUIN can reveal new isoform candidates. CONCLUSIONS: Regarding the increasing importance of quantitative proteomics we think that this method will be useful in practical applications like model fitting or functional enrichment analysis. We recommend to use this method if quantitation is a major objective of research.
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spelling pubmed-33687282012-06-07 PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios Bauer, Chris Kleinjung, Frank Rutishauser, Dorothea Panse, Christian Chadt, Alexandra Dreja, Tanja Al-Hasani, Hadi Reinert, Knut Schlapbach, Ralph Schuchhardt, Johannes BMC Bioinformatics Methodology Article BACKGROUND: Recent development of novel technologies paved the way for quantitative proteomics. One of the most important among them is iTRAQ, employing isobaric tags for relative or absolute quantitation. Despite large progress in technology development, still many challenges remain for derivation and interpretation of quantitative results. One of these challenges is the consistent assignment of peptides to proteins. RESULTS: We have developed Peptide Profiling Guided Identification of Proteins (PPINGUIN), a statistical analysis workflow for iTRAQ data addressing the problem of ambiguous peptide quantitations. Motivated by the assumption that peptides uniquely derived from the same protein are correlated, our method employs clustering as a very early step in data processing prior to protein inference. Our method increases experimental reproducibility and decreases variability of quantitations of peptides assigned to the same protein. Giving further support to our method, application to a type 2 diabetes dataset identifies a list of protein candidates that is in very good agreement with previously performed transcriptomics meta analysis. Making use of quantitative properties of signal patterns identified, PPINGUIN can reveal new isoform candidates. CONCLUSIONS: Regarding the increasing importance of quantitative proteomics we think that this method will be useful in practical applications like model fitting or functional enrichment analysis. We recommend to use this method if quantitation is a major objective of research. BioMed Central 2012-02-16 /pmc/articles/PMC3368728/ /pubmed/22340093 http://dx.doi.org/10.1186/1471-2105-13-34 Text en Copyright ©2012 Bauer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Bauer, Chris
Kleinjung, Frank
Rutishauser, Dorothea
Panse, Christian
Chadt, Alexandra
Dreja, Tanja
Al-Hasani, Hadi
Reinert, Knut
Schlapbach, Ralph
Schuchhardt, Johannes
PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios
title PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios
title_full PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios
title_fullStr PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios
title_full_unstemmed PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios
title_short PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratios
title_sort ppinguin: peptide profiling guided identification of proteins improves quantitation of itraq ratios
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368728/
https://www.ncbi.nlm.nih.gov/pubmed/22340093
http://dx.doi.org/10.1186/1471-2105-13-34
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