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Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor
Ultrasensitive, versatile sensors for molecular biomarkers are a critical component of disease diagnostics and personalized medicine as the COVID-19 pandemic has revealed in dramatic fashion. Integrated electrical nanopore sensors can fill this need via label-free, direct detection of individual bio...
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/PMC8400458/ https://www.ncbi.nlm.nih.gov/pubmed/34474277 http://dx.doi.org/10.1016/j.bios.2021.113588 |
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author | Sampad, Mohammad Julker Neyen Zhang, Han Yuzvinsky, Thomas D. Stott, Matthew A. Hawkins, Aaron R. Schmidt, Holger |
author_facet | Sampad, Mohammad Julker Neyen Zhang, Han Yuzvinsky, Thomas D. Stott, Matthew A. Hawkins, Aaron R. Schmidt, Holger |
author_sort | Sampad, Mohammad Julker Neyen |
collection | PubMed |
description | Ultrasensitive, versatile sensors for molecular biomarkers are a critical component of disease diagnostics and personalized medicine as the COVID-19 pandemic has revealed in dramatic fashion. Integrated electrical nanopore sensors can fill this need via label-free, direct detection of individual biomolecules, but a fully functional device for clinical sample analysis has yet to be developed. Here, we report amplification-free detection of SARS-CoV-2 RNAs with single molecule sensitivity from clinical nasopharyngeal swab samples on an electro-optofluidic chip. The device relies on optically assisted delivery of target carrying microbeads to the nanopore for single RNA detection after release. A sensing rate enhancement of over 2,000x with favorable scaling towards lower concentrations is demonstrated. The combination of target specificity, chip-scale integration and rapid detection ensures the practicality of this approach for COVID-19 diagnosis over the entire clinically relevant concentration range from 10(4)-10(9) copies/mL. |
format | Online Article Text |
id | pubmed-8400458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84004582021-08-30 Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor Sampad, Mohammad Julker Neyen Zhang, Han Yuzvinsky, Thomas D. Stott, Matthew A. Hawkins, Aaron R. Schmidt, Holger Biosens Bioelectron Article Ultrasensitive, versatile sensors for molecular biomarkers are a critical component of disease diagnostics and personalized medicine as the COVID-19 pandemic has revealed in dramatic fashion. Integrated electrical nanopore sensors can fill this need via label-free, direct detection of individual biomolecules, but a fully functional device for clinical sample analysis has yet to be developed. Here, we report amplification-free detection of SARS-CoV-2 RNAs with single molecule sensitivity from clinical nasopharyngeal swab samples on an electro-optofluidic chip. The device relies on optically assisted delivery of target carrying microbeads to the nanopore for single RNA detection after release. A sensing rate enhancement of over 2,000x with favorable scaling towards lower concentrations is demonstrated. The combination of target specificity, chip-scale integration and rapid detection ensures the practicality of this approach for COVID-19 diagnosis over the entire clinically relevant concentration range from 10(4)-10(9) copies/mL. Elsevier B.V. 2021-12-15 2021-08-28 /pmc/articles/PMC8400458/ /pubmed/34474277 http://dx.doi.org/10.1016/j.bios.2021.113588 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 Sampad, Mohammad Julker Neyen Zhang, Han Yuzvinsky, Thomas D. Stott, Matthew A. Hawkins, Aaron R. Schmidt, Holger Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor |
title | Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor |
title_full | Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor |
title_fullStr | Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor |
title_full_unstemmed | Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor |
title_short | Optical trapping assisted label-free and amplification-free detection of SARS-CoV-2 RNAs with an optofluidic nanopore sensor |
title_sort | optical trapping assisted label-free and amplification-free detection of sars-cov-2 rnas with an optofluidic nanopore sensor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400458/ https://www.ncbi.nlm.nih.gov/pubmed/34474277 http://dx.doi.org/10.1016/j.bios.2021.113588 |
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