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Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera
Biomarkers, including cytokines, can help in the diagnosis, prognosis, and prediction of treatment response across a wide range of disease settings. Consequently, the recent emergence of protein microarray technology, which is able to quantify a range of inflammatory mediators in a large number of s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213990/ https://www.ncbi.nlm.nih.gov/pubmed/25382942 http://dx.doi.org/10.1155/2014/820304 |
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author | Selvarajah, Senthooran Negm, Ola H. Hamed, Mohamed R. Tubby, Carolyn Todd, Ian Tighe, Patrick J. Harrison, Tim Fairclough, Lucy C. |
author_facet | Selvarajah, Senthooran Negm, Ola H. Hamed, Mohamed R. Tubby, Carolyn Todd, Ian Tighe, Patrick J. Harrison, Tim Fairclough, Lucy C. |
author_sort | Selvarajah, Senthooran |
collection | PubMed |
description | Biomarkers, including cytokines, can help in the diagnosis, prognosis, and prediction of treatment response across a wide range of disease settings. Consequently, the recent emergence of protein microarray technology, which is able to quantify a range of inflammatory mediators in a large number of samples simultaneously, has become highly desirable. However, the cost of commercial systems remains somewhat prohibitive. Here we show the development, validation, and implementation of an in-house microarray platform which enables the simultaneous quantitative analysis of multiple protein biomarkers. The accuracy and precision of the in-house microarray system were investigated according to the Food and Drug Administration (FDA) guidelines for pharmacokinetic assay validation. The assay fell within these limits for all but the very low-abundant cytokines, such as interleukin- (IL-) 10. Additionally, there were no significant differences between cytokine detection using our microarray system and the “gold standard” ELISA format. Crucially, future biomarker detection need not be limited to the 16 cytokines shown here but could be expanded as required. In conclusion, we detail a bespoke protein microarray system, utilizing well-validated ELISA reagents, that allows accurate, precise, and reproducible multiplexed biomarker quantification, comparable with commercial ELISA, and allowing customization beyond that of similar commercial microarrays. |
format | Online Article Text |
id | pubmed-4213990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42139902014-11-09 Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera Selvarajah, Senthooran Negm, Ola H. Hamed, Mohamed R. Tubby, Carolyn Todd, Ian Tighe, Patrick J. Harrison, Tim Fairclough, Lucy C. Mediators Inflamm Research Article Biomarkers, including cytokines, can help in the diagnosis, prognosis, and prediction of treatment response across a wide range of disease settings. Consequently, the recent emergence of protein microarray technology, which is able to quantify a range of inflammatory mediators in a large number of samples simultaneously, has become highly desirable. However, the cost of commercial systems remains somewhat prohibitive. Here we show the development, validation, and implementation of an in-house microarray platform which enables the simultaneous quantitative analysis of multiple protein biomarkers. The accuracy and precision of the in-house microarray system were investigated according to the Food and Drug Administration (FDA) guidelines for pharmacokinetic assay validation. The assay fell within these limits for all but the very low-abundant cytokines, such as interleukin- (IL-) 10. Additionally, there were no significant differences between cytokine detection using our microarray system and the “gold standard” ELISA format. Crucially, future biomarker detection need not be limited to the 16 cytokines shown here but could be expanded as required. In conclusion, we detail a bespoke protein microarray system, utilizing well-validated ELISA reagents, that allows accurate, precise, and reproducible multiplexed biomarker quantification, comparable with commercial ELISA, and allowing customization beyond that of similar commercial microarrays. Hindawi Publishing Corporation 2014 2014-10-14 /pmc/articles/PMC4213990/ /pubmed/25382942 http://dx.doi.org/10.1155/2014/820304 Text en Copyright © 2014 Senthooran Selvarajah 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 Selvarajah, Senthooran Negm, Ola H. Hamed, Mohamed R. Tubby, Carolyn Todd, Ian Tighe, Patrick J. Harrison, Tim Fairclough, Lucy C. Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera |
title | Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera |
title_full | Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera |
title_fullStr | Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera |
title_full_unstemmed | Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera |
title_short | Development and Validation of Protein Microarray Technology for Simultaneous Inflammatory Mediator Detection in Human Sera |
title_sort | development and validation of protein microarray technology for simultaneous inflammatory mediator detection in human sera |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213990/ https://www.ncbi.nlm.nih.gov/pubmed/25382942 http://dx.doi.org/10.1155/2014/820304 |
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