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A Versatile Microarray Platform for Capturing Rare Cells
Analyses of rare events occurring at extremely low frequencies in body fluids are still challenging. We established a versatile microarray-based platform able to capture single target cells from large background populations. As use case we chose the challenging application of detecting circulating t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615978/ https://www.ncbi.nlm.nih.gov/pubmed/26493176 http://dx.doi.org/10.1038/srep15342 |
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author | Brinkmann, Falko Hirtz, Michael Haller, Anna Gorges, Tobias M. Vellekoop, Michael J. Riethdorf, Sabine Müller, Volkmar Pantel, Klaus Fuchs, Harald |
author_facet | Brinkmann, Falko Hirtz, Michael Haller, Anna Gorges, Tobias M. Vellekoop, Michael J. Riethdorf, Sabine Müller, Volkmar Pantel, Klaus Fuchs, Harald |
author_sort | Brinkmann, Falko |
collection | PubMed |
description | Analyses of rare events occurring at extremely low frequencies in body fluids are still challenging. We established a versatile microarray-based platform able to capture single target cells from large background populations. As use case we chose the challenging application of detecting circulating tumor cells (CTCs) – about one cell in a billion normal blood cells. After incubation with an antibody cocktail, targeted cells are extracted on a microarray in a microfluidic chip. The accessibility of our platform allows for subsequent recovery of targets for further analysis. The microarray facilitates exclusion of false positive capture events by co-localization allowing for detection without fluorescent labelling. Analyzing blood samples from cancer patients with our platform reached and partly outreached gold standard performance, demonstrating feasibility for clinical application. Clinical researchers free choice of antibody cocktail without need for altered chip manufacturing or incubation protocol, allows virtual arbitrary targeting of capture species and therefore wide spread applications in biomedical sciences. |
format | Online Article Text |
id | pubmed-4615978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46159782015-10-29 A Versatile Microarray Platform for Capturing Rare Cells Brinkmann, Falko Hirtz, Michael Haller, Anna Gorges, Tobias M. Vellekoop, Michael J. Riethdorf, Sabine Müller, Volkmar Pantel, Klaus Fuchs, Harald Sci Rep Article Analyses of rare events occurring at extremely low frequencies in body fluids are still challenging. We established a versatile microarray-based platform able to capture single target cells from large background populations. As use case we chose the challenging application of detecting circulating tumor cells (CTCs) – about one cell in a billion normal blood cells. After incubation with an antibody cocktail, targeted cells are extracted on a microarray in a microfluidic chip. The accessibility of our platform allows for subsequent recovery of targets for further analysis. The microarray facilitates exclusion of false positive capture events by co-localization allowing for detection without fluorescent labelling. Analyzing blood samples from cancer patients with our platform reached and partly outreached gold standard performance, demonstrating feasibility for clinical application. Clinical researchers free choice of antibody cocktail without need for altered chip manufacturing or incubation protocol, allows virtual arbitrary targeting of capture species and therefore wide spread applications in biomedical sciences. Nature Publishing Group 2015-10-23 /pmc/articles/PMC4615978/ /pubmed/26493176 http://dx.doi.org/10.1038/srep15342 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Brinkmann, Falko Hirtz, Michael Haller, Anna Gorges, Tobias M. Vellekoop, Michael J. Riethdorf, Sabine Müller, Volkmar Pantel, Klaus Fuchs, Harald A Versatile Microarray Platform for Capturing Rare Cells |
title | A Versatile Microarray Platform for Capturing Rare Cells |
title_full | A Versatile Microarray Platform for Capturing Rare Cells |
title_fullStr | A Versatile Microarray Platform for Capturing Rare Cells |
title_full_unstemmed | A Versatile Microarray Platform for Capturing Rare Cells |
title_short | A Versatile Microarray Platform for Capturing Rare Cells |
title_sort | versatile microarray platform for capturing rare cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615978/ https://www.ncbi.nlm.nih.gov/pubmed/26493176 http://dx.doi.org/10.1038/srep15342 |
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