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Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics
Accurate and accessible nucleic acid diagnostics is critical to reducing the spread of COVID-19 and resuming socioeconomic activities. Here, we present an integrated platform for the direct detection of SARS-CoV-2 RNA targets near patients. Termed electrochemical system integrating reconfigurable en...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435073/ https://www.ncbi.nlm.nih.gov/pubmed/34534949 http://dx.doi.org/10.1016/j.bios.2021.113629 |
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author | Zhao, Haitao Zhang, Yan Chen, Yuan Ho, Nicholas R.Y. Sundah, Noah R. Natalia, Auginia Liu, Yu Miow, Qing Hao Wang, Yu Tambyah, Paul A. Ong, Catherine W.M. Shao, Huilin |
author_facet | Zhao, Haitao Zhang, Yan Chen, Yuan Ho, Nicholas R.Y. Sundah, Noah R. Natalia, Auginia Liu, Yu Miow, Qing Hao Wang, Yu Tambyah, Paul A. Ong, Catherine W.M. Shao, Huilin |
author_sort | Zhao, Haitao |
collection | PubMed |
description | Accurate and accessible nucleic acid diagnostics is critical to reducing the spread of COVID-19 and resuming socioeconomic activities. Here, we present an integrated platform for the direct detection of SARS-CoV-2 RNA targets near patients. Termed electrochemical system integrating reconfigurable enzyme-DNA nanostructures (eSIREN), the technology leverages responsive molecular nanostructures and automated microfluidics to seamlessly transduce target-induced molecular activation into an enhanced electrochemical signal. Through responsive enzyme-DNA nanostructures, the technology establishes a molecular circuitry that directly recognizes specific RNA targets and catalytically enhances signaling; only upon target hybridization, the molecular nanostructures activate to liberate strong enzymatic activity and initiate cascading reactions. Through automated microfluidics, the system coordinates and interfaces the molecular circuitry with embedded electronics; its pressure actuation and liquid-guiding structures improve not only analytical performance but also automated implementation. The developed platform establishes a detection limit of 7 copies of RNA target per μl, operates against the complex biological background of native patient samples, and is completed in <20 min at room temperature. When clinically evaluated, the technology demonstrates accurate detection in extracted RNA samples and direct swab lysates to diagnose COVID-19 patients. |
format | Online Article Text |
id | pubmed-8435073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84350732021-09-13 Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics Zhao, Haitao Zhang, Yan Chen, Yuan Ho, Nicholas R.Y. Sundah, Noah R. Natalia, Auginia Liu, Yu Miow, Qing Hao Wang, Yu Tambyah, Paul A. Ong, Catherine W.M. Shao, Huilin Biosens Bioelectron Article Accurate and accessible nucleic acid diagnostics is critical to reducing the spread of COVID-19 and resuming socioeconomic activities. Here, we present an integrated platform for the direct detection of SARS-CoV-2 RNA targets near patients. Termed electrochemical system integrating reconfigurable enzyme-DNA nanostructures (eSIREN), the technology leverages responsive molecular nanostructures and automated microfluidics to seamlessly transduce target-induced molecular activation into an enhanced electrochemical signal. Through responsive enzyme-DNA nanostructures, the technology establishes a molecular circuitry that directly recognizes specific RNA targets and catalytically enhances signaling; only upon target hybridization, the molecular nanostructures activate to liberate strong enzymatic activity and initiate cascading reactions. Through automated microfluidics, the system coordinates and interfaces the molecular circuitry with embedded electronics; its pressure actuation and liquid-guiding structures improve not only analytical performance but also automated implementation. The developed platform establishes a detection limit of 7 copies of RNA target per μl, operates against the complex biological background of native patient samples, and is completed in <20 min at room temperature. When clinically evaluated, the technology demonstrates accurate detection in extracted RNA samples and direct swab lysates to diagnose COVID-19 patients. Elsevier B.V. 2021-12-15 2021-09-12 /pmc/articles/PMC8435073/ /pubmed/34534949 http://dx.doi.org/10.1016/j.bios.2021.113629 Text en © 2021 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Zhao, Haitao Zhang, Yan Chen, Yuan Ho, Nicholas R.Y. Sundah, Noah R. Natalia, Auginia Liu, Yu Miow, Qing Hao Wang, Yu Tambyah, Paul A. Ong, Catherine W.M. Shao, Huilin Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics |
title | Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics |
title_full | Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics |
title_fullStr | Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics |
title_full_unstemmed | Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics |
title_short | Accessible detection of SARS-CoV-2 through molecular nanostructures and automated microfluidics |
title_sort | accessible detection of sars-cov-2 through molecular nanostructures and automated microfluidics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435073/ https://www.ncbi.nlm.nih.gov/pubmed/34534949 http://dx.doi.org/10.1016/j.bios.2021.113629 |
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