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Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays

MicroRNAs (miRNAs) have recently emerged as promising biomarkers for the profiling of diseases. Translation of miRNA biomarkers to clinical practice, however, remains a challenge due to the lack of analysis platforms for sensitive, quantitative, and multiplex miRNA assays that have simple and robust...

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Autores principales: Tentori, Augusto M., Nagarajan, Maxwell B., Kim, Jae Jung, Zhang, Wen Cai, Slack, Frank J., Doyle, Patrick S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081239/
https://www.ncbi.nlm.nih.gov/pubmed/29998262
http://dx.doi.org/10.1039/c8lc00498f
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author Tentori, Augusto M.
Nagarajan, Maxwell B.
Kim, Jae Jung
Zhang, Wen Cai
Slack, Frank J.
Doyle, Patrick S.
author_facet Tentori, Augusto M.
Nagarajan, Maxwell B.
Kim, Jae Jung
Zhang, Wen Cai
Slack, Frank J.
Doyle, Patrick S.
author_sort Tentori, Augusto M.
collection PubMed
description MicroRNAs (miRNAs) have recently emerged as promising biomarkers for the profiling of diseases. Translation of miRNA biomarkers to clinical practice, however, remains a challenge due to the lack of analysis platforms for sensitive, quantitative, and multiplex miRNA assays that have simple and robust workflows suitable for translation. The platform we present here utilizes functionalized hydrogel posts contained within isolated nanoliter well reactors for quantitative and multiplex assays directly from unprocessed cell samples without the need of prior nucleic acid extraction. Simultaneous reactor isolation and delivery of miRNA extraction reagents is achieved by sealing an array of wells containing the functionalized hydrogel posts and cells against another array of wells containing lysis and extraction reagents. The nanoliter well array platform features >100× better sensitivity compared to previous technology utilizing hydrogel particles without relying on signal amplification and enables >100 parallel assays in a single device. These advances provided by this platform lay the groundwork for translatable and robust analysis technologies for miRNA expression profiling in samples with small populations of cells and in precious, material-limited samples.
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spelling pubmed-60812392018-08-08 Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays Tentori, Augusto M. Nagarajan, Maxwell B. Kim, Jae Jung Zhang, Wen Cai Slack, Frank J. Doyle, Patrick S. Lab Chip Chemistry MicroRNAs (miRNAs) have recently emerged as promising biomarkers for the profiling of diseases. Translation of miRNA biomarkers to clinical practice, however, remains a challenge due to the lack of analysis platforms for sensitive, quantitative, and multiplex miRNA assays that have simple and robust workflows suitable for translation. The platform we present here utilizes functionalized hydrogel posts contained within isolated nanoliter well reactors for quantitative and multiplex assays directly from unprocessed cell samples without the need of prior nucleic acid extraction. Simultaneous reactor isolation and delivery of miRNA extraction reagents is achieved by sealing an array of wells containing the functionalized hydrogel posts and cells against another array of wells containing lysis and extraction reagents. The nanoliter well array platform features >100× better sensitivity compared to previous technology utilizing hydrogel particles without relying on signal amplification and enables >100 parallel assays in a single device. These advances provided by this platform lay the groundwork for translatable and robust analysis technologies for miRNA expression profiling in samples with small populations of cells and in precious, material-limited samples. Royal Society of Chemistry 2018-08-21 2018-07-06 /pmc/articles/PMC6081239/ /pubmed/29998262 http://dx.doi.org/10.1039/c8lc00498f Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Tentori, Augusto M.
Nagarajan, Maxwell B.
Kim, Jae Jung
Zhang, Wen Cai
Slack, Frank J.
Doyle, Patrick S.
Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays
title Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays
title_full Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays
title_fullStr Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays
title_full_unstemmed Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays
title_short Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays
title_sort quantitative and multiplex microrna assays from unprocessed cells in isolated nanoliter well arrays
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081239/
https://www.ncbi.nlm.nih.gov/pubmed/29998262
http://dx.doi.org/10.1039/c8lc00498f
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