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Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum
BACKGROUND: Proteolysis of matrix components, in particular elastin, is a major contributing factor to the development of lung diseases such as emphysema and chronic obstructive pulmonary disease (COPD). MMP-12 (macrophage elastase) is a protease known to be involved in the progression of lung disea...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921351/ https://www.ncbi.nlm.nih.gov/pubmed/20678199 http://dx.doi.org/10.1186/1471-2466-10-40 |
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author | LaPan, Peter Brady, Jeff Grierson, Christal Fleming, Margaret Miller, Doug Sypek, Joe Fu, Bin |
author_facet | LaPan, Peter Brady, Jeff Grierson, Christal Fleming, Margaret Miller, Doug Sypek, Joe Fu, Bin |
author_sort | LaPan, Peter |
collection | PubMed |
description | BACKGROUND: Proteolysis of matrix components, in particular elastin, is a major contributing factor to the development of lung diseases such as emphysema and chronic obstructive pulmonary disease (COPD). MMP-12 (macrophage elastase) is a protease known to be involved in the progression of lung disease. The relatively low abundance of MMP-12 has precluded the development of quantitative assays that can accurately measure MMP-12 protein levels and activity across cohorts of healthy and diseased individuals. METHODS: Commercial antibodies were screened for performance in sandwich ELISA and capture FRET activity assay formats. Precision, accuracy, sensitivity, dilution linearity, and spike recovery were evaluated using sputum samples. RESULTS: Total protein and capture FRET activity assays were developed that were sensitive enough to detect MMP-12 in 37 of 38 donor sputum samples. A comparison of results between the two assays shows that a majority of sputum MMP-12 is in the active form. No differences were seen between normal, asthmatic, and COPD donors. CONCLUSION: Sensitive and quantitative assays for both MMP-12 activity and total protein in human induced sputum have been developed. These assays can be used to evaluate MMP-12 as a biomarker for lung disease, and to monitor efficacy of potential therapeutic compounds. |
format | Text |
id | pubmed-2921351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29213512010-08-14 Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum LaPan, Peter Brady, Jeff Grierson, Christal Fleming, Margaret Miller, Doug Sypek, Joe Fu, Bin BMC Pulm Med Technical Advance BACKGROUND: Proteolysis of matrix components, in particular elastin, is a major contributing factor to the development of lung diseases such as emphysema and chronic obstructive pulmonary disease (COPD). MMP-12 (macrophage elastase) is a protease known to be involved in the progression of lung disease. The relatively low abundance of MMP-12 has precluded the development of quantitative assays that can accurately measure MMP-12 protein levels and activity across cohorts of healthy and diseased individuals. METHODS: Commercial antibodies were screened for performance in sandwich ELISA and capture FRET activity assay formats. Precision, accuracy, sensitivity, dilution linearity, and spike recovery were evaluated using sputum samples. RESULTS: Total protein and capture FRET activity assays were developed that were sensitive enough to detect MMP-12 in 37 of 38 donor sputum samples. A comparison of results between the two assays shows that a majority of sputum MMP-12 is in the active form. No differences were seen between normal, asthmatic, and COPD donors. CONCLUSION: Sensitive and quantitative assays for both MMP-12 activity and total protein in human induced sputum have been developed. These assays can be used to evaluate MMP-12 as a biomarker for lung disease, and to monitor efficacy of potential therapeutic compounds. BioMed Central 2010-08-02 /pmc/articles/PMC2921351/ /pubmed/20678199 http://dx.doi.org/10.1186/1471-2466-10-40 Text en Copyright ©2010 LaPan 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 | Technical Advance LaPan, Peter Brady, Jeff Grierson, Christal Fleming, Margaret Miller, Doug Sypek, Joe Fu, Bin Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum |
title | Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum |
title_full | Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum |
title_fullStr | Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum |
title_full_unstemmed | Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum |
title_short | Optimization of total protein and activity assays for the detection of MMP-12 in induced human sputum |
title_sort | optimization of total protein and activity assays for the detection of mmp-12 in induced human sputum |
topic | Technical Advance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921351/ https://www.ncbi.nlm.nih.gov/pubmed/20678199 http://dx.doi.org/10.1186/1471-2466-10-40 |
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