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iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections

Both isobaric tags for relative and absolute quantitation (iTRAQ) and label-free methods are widely used for quantitative proteomics. Here, we provide a detailed evaluation of these proteomics approaches based on large datasets from biological samples. iTRAQ-label-based and label-free quantitations...

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Autores principales: Trinh, Hung V., Grossmann, Jonas, Gehrig, Peter, Roschitzki, Bernd, Schlapbach, Ralph, Greber, Urs F., Hemmi, Silvio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608280/
https://www.ncbi.nlm.nih.gov/pubmed/23555056
http://dx.doi.org/10.1155/2013/581862
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author Trinh, Hung V.
Grossmann, Jonas
Gehrig, Peter
Roschitzki, Bernd
Schlapbach, Ralph
Greber, Urs F.
Hemmi, Silvio
author_facet Trinh, Hung V.
Grossmann, Jonas
Gehrig, Peter
Roschitzki, Bernd
Schlapbach, Ralph
Greber, Urs F.
Hemmi, Silvio
author_sort Trinh, Hung V.
collection PubMed
description Both isobaric tags for relative and absolute quantitation (iTRAQ) and label-free methods are widely used for quantitative proteomics. Here, we provide a detailed evaluation of these proteomics approaches based on large datasets from biological samples. iTRAQ-label-based and label-free quantitations were compared using protein lysate samples from noninfected human lung epithelial A549 cells and from cells infected for 24 h with human adenovirus type 3 or type 5. Either iTRAQ-label-based or label-free methods were used, and the resulting samples were analyzed by liquid chromatography (LC) and tandem mass spectrometry (MS/MS). To reduce a possible bias from quantitation software, we applied several software packages for each procedure. ProteinPilot and Scaffold Q+ software were used for iTRAQ-labeled samples, while Progenesis LC-MS and ProgenesisF-T2PQ/T3PQ were employed for label-free analyses. R (2) correlation coefficients correlated well between two software packages applied to the same datasets with values between 0.48 and 0.78 for iTRAQ-label-based quantitations and 0.5 and 0.86 for label-free quantitations. Analyses of label-free samples showed higher levels of protein up- or downregulation in comparison to iTRAQ-labeled samples. The concentration differences were further evaluated by Western blotting for four downregulated proteins. These data suggested that the label-free method was more accurate than the iTRAQ method.
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spelling pubmed-36082802013-04-02 iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections Trinh, Hung V. Grossmann, Jonas Gehrig, Peter Roschitzki, Bernd Schlapbach, Ralph Greber, Urs F. Hemmi, Silvio Int J Proteomics Research Article Both isobaric tags for relative and absolute quantitation (iTRAQ) and label-free methods are widely used for quantitative proteomics. Here, we provide a detailed evaluation of these proteomics approaches based on large datasets from biological samples. iTRAQ-label-based and label-free quantitations were compared using protein lysate samples from noninfected human lung epithelial A549 cells and from cells infected for 24 h with human adenovirus type 3 or type 5. Either iTRAQ-label-based or label-free methods were used, and the resulting samples were analyzed by liquid chromatography (LC) and tandem mass spectrometry (MS/MS). To reduce a possible bias from quantitation software, we applied several software packages for each procedure. ProteinPilot and Scaffold Q+ software were used for iTRAQ-labeled samples, while Progenesis LC-MS and ProgenesisF-T2PQ/T3PQ were employed for label-free analyses. R (2) correlation coefficients correlated well between two software packages applied to the same datasets with values between 0.48 and 0.78 for iTRAQ-label-based quantitations and 0.5 and 0.86 for label-free quantitations. Analyses of label-free samples showed higher levels of protein up- or downregulation in comparison to iTRAQ-labeled samples. The concentration differences were further evaluated by Western blotting for four downregulated proteins. These data suggested that the label-free method was more accurate than the iTRAQ method. Hindawi Publishing Corporation 2013 2013-03-11 /pmc/articles/PMC3608280/ /pubmed/23555056 http://dx.doi.org/10.1155/2013/581862 Text en Copyright © 2013 Hung V. Trinh 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
Trinh, Hung V.
Grossmann, Jonas
Gehrig, Peter
Roschitzki, Bernd
Schlapbach, Ralph
Greber, Urs F.
Hemmi, Silvio
iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections
title iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections
title_full iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections
title_fullStr iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections
title_full_unstemmed iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections
title_short iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections
title_sort itraq-based and label-free proteomics approaches for studies of human adenovirus infections
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608280/
https://www.ncbi.nlm.nih.gov/pubmed/23555056
http://dx.doi.org/10.1155/2013/581862
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