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Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification
BACKGROUND: Reverse phase protein arrays (RPPA) emerged as a useful experimental platform to analyze biological samples in a high-throughput format. Different signal detection methods have been described to generate a quantitative readout on RPPA including the use of fluorescently labeled antibodies...
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/PMC2908584/ https://www.ncbi.nlm.nih.gov/pubmed/20569466 http://dx.doi.org/10.1186/1477-5956-8-36 |
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author | Brase, Jan C Mannsperger, Heiko Fröhlich, Holger Gade, Stephan Schmidt, Christian Wiemann, Stefan Beissbarth, Tim Schlomm, Thorsten Sültmann, Holger Korf, Ulrike |
author_facet | Brase, Jan C Mannsperger, Heiko Fröhlich, Holger Gade, Stephan Schmidt, Christian Wiemann, Stefan Beissbarth, Tim Schlomm, Thorsten Sültmann, Holger Korf, Ulrike |
author_sort | Brase, Jan C |
collection | PubMed |
description | BACKGROUND: Reverse phase protein arrays (RPPA) emerged as a useful experimental platform to analyze biological samples in a high-throughput format. Different signal detection methods have been described to generate a quantitative readout on RPPA including the use of fluorescently labeled antibodies. Increasing the sensitivity of RPPA approaches is important since many signaling proteins or posttranslational modifications are present at a low level. RESULTS: A new antibody-mediated signal amplification (AMSA) strategy relying on sequential incubation steps with fluorescently-labeled secondary antibodies reactive against each other is introduced here. The signal quantification is performed in the near-infrared range. The RPPA-based analysis of 14 endogenous proteins in seven different cell lines demonstrated a strong correlation (r = 0.89) between AMSA and standard NIR detection. Probing serial dilutions of human cancer cell lines with different primary antibodies demonstrated that the new amplification approach improved the limit of detection especially for low abundant target proteins. CONCLUSIONS: Antibody-mediated signal amplification is a convenient and cost-effective approach for the robust and specific quantification of low abundant proteins on RPPAs. Contrasting other amplification approaches it allows target protein detection over a large linear range. |
format | Text |
id | pubmed-2908584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29085842010-07-23 Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification Brase, Jan C Mannsperger, Heiko Fröhlich, Holger Gade, Stephan Schmidt, Christian Wiemann, Stefan Beissbarth, Tim Schlomm, Thorsten Sültmann, Holger Korf, Ulrike Proteome Sci Methodology BACKGROUND: Reverse phase protein arrays (RPPA) emerged as a useful experimental platform to analyze biological samples in a high-throughput format. Different signal detection methods have been described to generate a quantitative readout on RPPA including the use of fluorescently labeled antibodies. Increasing the sensitivity of RPPA approaches is important since many signaling proteins or posttranslational modifications are present at a low level. RESULTS: A new antibody-mediated signal amplification (AMSA) strategy relying on sequential incubation steps with fluorescently-labeled secondary antibodies reactive against each other is introduced here. The signal quantification is performed in the near-infrared range. The RPPA-based analysis of 14 endogenous proteins in seven different cell lines demonstrated a strong correlation (r = 0.89) between AMSA and standard NIR detection. Probing serial dilutions of human cancer cell lines with different primary antibodies demonstrated that the new amplification approach improved the limit of detection especially for low abundant target proteins. CONCLUSIONS: Antibody-mediated signal amplification is a convenient and cost-effective approach for the robust and specific quantification of low abundant proteins on RPPAs. Contrasting other amplification approaches it allows target protein detection over a large linear range. BioMed Central 2010-06-22 /pmc/articles/PMC2908584/ /pubmed/20569466 http://dx.doi.org/10.1186/1477-5956-8-36 Text en Copyright ©2010 Brase 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 | Methodology Brase, Jan C Mannsperger, Heiko Fröhlich, Holger Gade, Stephan Schmidt, Christian Wiemann, Stefan Beissbarth, Tim Schlomm, Thorsten Sültmann, Holger Korf, Ulrike Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification |
title | Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification |
title_full | Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification |
title_fullStr | Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification |
title_full_unstemmed | Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification |
title_short | Increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification |
title_sort | increasing the sensitivity of reverse phase protein arrays by antibody-mediated signal amplification |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908584/ https://www.ncbi.nlm.nih.gov/pubmed/20569466 http://dx.doi.org/10.1186/1477-5956-8-36 |
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