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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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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. |
format | Online Article Text |
id | pubmed-3608280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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