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

<p>Abstract</p> <p>Background</p> <p>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 de...

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Main Authors: Bauer Chris, Kleinjung Frank, Rutishauser Dorothea, Panse Christian, Chadt Alexandra, Dreja Tanja, Al-Hasani Hadi, Reinert Knut, Schlapbach Ralph, Schuchhardt Johannes
Format: Article
Language:English
Published: BMC 2012-02-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/13/34
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spelling doaj-50017622b1ec4ac086f65c9df197dd662020-11-24T21:39:42ZengBMCBMC Bioinformatics1471-21052012-02-011313410.1186/1471-2105-13-34PPINGUIN: Peptide Profiling Guided Identification of Proteins improves quantitation of iTRAQ ratiosBauer ChrisKleinjung FrankRutishauser DorotheaPanse ChristianChadt AlexandraDreja TanjaAl-Hasani HadiReinert KnutSchlapbach RalphSchuchhardt Johannes<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p> http://www.biomedcentral.com/1471-2105/13/34
collection DOAJ
language English
format Article
sources DOAJ
author Bauer Chris
Kleinjung Frank
Rutishauser Dorothea
Panse Christian
Chadt Alexandra
Dreja Tanja
Al-Hasani Hadi
Reinert Knut
Schlapbach Ralph
Schuchhardt Johannes
spellingShingle 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
BMC Bioinformatics
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
title 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_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_sort ppinguin: peptide profiling guided identification of proteins improves quantitation of itraq ratios
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2012-02-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>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.</p>
url http://www.biomedcentral.com/1471-2105/13/34
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