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A lab-on-a-chip for rapid miRNA extraction

We present a simple to operate microfluidic chip system that allows for the extraction of miRNAs from cells with minimal hands-on time. The chip integrates thermoelectric lysis (TEL) of cells with native gel-electrophoretic elution (GEE) of released nucleic acids and uses non-toxic reagents while re...

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Detalles Bibliográficos
Autores principales: Behrmann, Ole, Hügle, Matthias, Bronsert, Peter, Herde, Bettina, Heni, Julian, Schramm, Marina, Hufert, Frank T., Urban, Gerald A., Dame, Gregory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6922460/
https://www.ncbi.nlm.nih.gov/pubmed/31856234
http://dx.doi.org/10.1371/journal.pone.0226571
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author Behrmann, Ole
Hügle, Matthias
Bronsert, Peter
Herde, Bettina
Heni, Julian
Schramm, Marina
Hufert, Frank T.
Urban, Gerald A.
Dame, Gregory
author_facet Behrmann, Ole
Hügle, Matthias
Bronsert, Peter
Herde, Bettina
Heni, Julian
Schramm, Marina
Hufert, Frank T.
Urban, Gerald A.
Dame, Gregory
author_sort Behrmann, Ole
collection PubMed
description We present a simple to operate microfluidic chip system that allows for the extraction of miRNAs from cells with minimal hands-on time. The chip integrates thermoelectric lysis (TEL) of cells with native gel-electrophoretic elution (GEE) of released nucleic acids and uses non-toxic reagents while requiring a sample volume of only 5 μl. These properties as well as the fast process duration of 180 seconds make the system an ideal candidate to be part of fully integrated point-of-care applications for e.g. the diagnosis of cancerous tissue. GEE was characterized in comparison to state-of-the-art silica column (SC) based RNA recovery using the mirVana kit (Ambion) as a reference. A synthetic miRNA (miR16) as well as a synthetic snoRNA (SNORD48) were subjected to both GEE and SC. Subsequent detection by stem-loop RT-qPCR demonstrated a higher yield for miRNA recovery by GEE. SnoRNA recovery performance was found to be equal for GEE and SC, indicating yield dependence on RNA length. Coupled operation of the chip (TEL + GEE) was characterized using serial dilutions of 5 to 500 MCF7 cancer cells in suspension. Samples were split and cells were subjected to either on-chip extraction or SC. Eluted miRNAs were then detected by stem-loop RT-qPCR without any further pre-processing. The extraction yield from cells was found to be up to ~200-fold higher for the chip system under non-denaturing conditions. The ratio of eluted miRNAs is shown to be dependent on the degree of complexation with miRNA associated proteins by comparing miRNAs purified by GEE from heat-shock and proteinase-K based lysis.
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spelling pubmed-69224602020-01-07 A lab-on-a-chip for rapid miRNA extraction Behrmann, Ole Hügle, Matthias Bronsert, Peter Herde, Bettina Heni, Julian Schramm, Marina Hufert, Frank T. Urban, Gerald A. Dame, Gregory PLoS One Research Article We present a simple to operate microfluidic chip system that allows for the extraction of miRNAs from cells with minimal hands-on time. The chip integrates thermoelectric lysis (TEL) of cells with native gel-electrophoretic elution (GEE) of released nucleic acids and uses non-toxic reagents while requiring a sample volume of only 5 μl. These properties as well as the fast process duration of 180 seconds make the system an ideal candidate to be part of fully integrated point-of-care applications for e.g. the diagnosis of cancerous tissue. GEE was characterized in comparison to state-of-the-art silica column (SC) based RNA recovery using the mirVana kit (Ambion) as a reference. A synthetic miRNA (miR16) as well as a synthetic snoRNA (SNORD48) were subjected to both GEE and SC. Subsequent detection by stem-loop RT-qPCR demonstrated a higher yield for miRNA recovery by GEE. SnoRNA recovery performance was found to be equal for GEE and SC, indicating yield dependence on RNA length. Coupled operation of the chip (TEL + GEE) was characterized using serial dilutions of 5 to 500 MCF7 cancer cells in suspension. Samples were split and cells were subjected to either on-chip extraction or SC. Eluted miRNAs were then detected by stem-loop RT-qPCR without any further pre-processing. The extraction yield from cells was found to be up to ~200-fold higher for the chip system under non-denaturing conditions. The ratio of eluted miRNAs is shown to be dependent on the degree of complexation with miRNA associated proteins by comparing miRNAs purified by GEE from heat-shock and proteinase-K based lysis. Public Library of Science 2019-12-19 /pmc/articles/PMC6922460/ /pubmed/31856234 http://dx.doi.org/10.1371/journal.pone.0226571 Text en © 2019 Behrmann et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Behrmann, Ole
Hügle, Matthias
Bronsert, Peter
Herde, Bettina
Heni, Julian
Schramm, Marina
Hufert, Frank T.
Urban, Gerald A.
Dame, Gregory
A lab-on-a-chip for rapid miRNA extraction
title A lab-on-a-chip for rapid miRNA extraction
title_full A lab-on-a-chip for rapid miRNA extraction
title_fullStr A lab-on-a-chip for rapid miRNA extraction
title_full_unstemmed A lab-on-a-chip for rapid miRNA extraction
title_short A lab-on-a-chip for rapid miRNA extraction
title_sort lab-on-a-chip for rapid mirna extraction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6922460/
https://www.ncbi.nlm.nih.gov/pubmed/31856234
http://dx.doi.org/10.1371/journal.pone.0226571
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