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Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor
The outbreak of the coronavirus disease (COVID-19) pandemic caused by the novel coronavirus (SARS-CoV-2) has been declared an international public health crisis. It is essential to develop diagnostic tests that can quickly identify infected individuals to limit the spread of the virus and assign tre...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827295/ https://www.ncbi.nlm.nih.gov/pubmed/33429915 http://dx.doi.org/10.3390/s21020390 |
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author | Mojsoska, Biljana Larsen, Sylvester Olsen, Dorte Aalund Madsen, Jonna Skov Brandslund, Ivan Alatraktchi, Fatima AlZahra’a |
author_facet | Mojsoska, Biljana Larsen, Sylvester Olsen, Dorte Aalund Madsen, Jonna Skov Brandslund, Ivan Alatraktchi, Fatima AlZahra’a |
author_sort | Mojsoska, Biljana |
collection | PubMed |
description | The outbreak of the coronavirus disease (COVID-19) pandemic caused by the novel coronavirus (SARS-CoV-2) has been declared an international public health crisis. It is essential to develop diagnostic tests that can quickly identify infected individuals to limit the spread of the virus and assign treatment options. Herein, we report a proof-of-concept label-free electrochemical immunoassay for the rapid detection of SARS-CoV-2 virus via the spike surface protein. The assay consists of a graphene working electrode functionalized with anti-spike antibodies. The concept of the immunosensor is to detect the signal perturbation obtained from ferri/ferrocyanide measurements after binding of the antigen during 45 min of incubation with a sample. The absolute change in the [Fe(CN)(6)](3)−/(4−) current upon increasing antigen concentrations on the immunosensor surface was used to determine the detection range of the spike protein. The sensor was able to detect a specific signal above 260 nM (20 µg/mL) of subunit 1 of recombinant spike protein. Additionally, it was able to detect SARS-CoV-2 at a concentration of 5.5 × 10(5) PFU/mL, which is within the physiologically relevant concentration range. The novel immunosensor has a significantly faster analysis time than the standard qPCR and is operated by a portable device which can enable on-site diagnosis of infection. |
format | Online Article Text |
id | pubmed-7827295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78272952021-01-25 Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor Mojsoska, Biljana Larsen, Sylvester Olsen, Dorte Aalund Madsen, Jonna Skov Brandslund, Ivan Alatraktchi, Fatima AlZahra’a Sensors (Basel) Article The outbreak of the coronavirus disease (COVID-19) pandemic caused by the novel coronavirus (SARS-CoV-2) has been declared an international public health crisis. It is essential to develop diagnostic tests that can quickly identify infected individuals to limit the spread of the virus and assign treatment options. Herein, we report a proof-of-concept label-free electrochemical immunoassay for the rapid detection of SARS-CoV-2 virus via the spike surface protein. The assay consists of a graphene working electrode functionalized with anti-spike antibodies. The concept of the immunosensor is to detect the signal perturbation obtained from ferri/ferrocyanide measurements after binding of the antigen during 45 min of incubation with a sample. The absolute change in the [Fe(CN)(6)](3)−/(4−) current upon increasing antigen concentrations on the immunosensor surface was used to determine the detection range of the spike protein. The sensor was able to detect a specific signal above 260 nM (20 µg/mL) of subunit 1 of recombinant spike protein. Additionally, it was able to detect SARS-CoV-2 at a concentration of 5.5 × 10(5) PFU/mL, which is within the physiologically relevant concentration range. The novel immunosensor has a significantly faster analysis time than the standard qPCR and is operated by a portable device which can enable on-site diagnosis of infection. MDPI 2021-01-08 /pmc/articles/PMC7827295/ /pubmed/33429915 http://dx.doi.org/10.3390/s21020390 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mojsoska, Biljana Larsen, Sylvester Olsen, Dorte Aalund Madsen, Jonna Skov Brandslund, Ivan Alatraktchi, Fatima AlZahra’a Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor |
title | Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor |
title_full | Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor |
title_fullStr | Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor |
title_full_unstemmed | Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor |
title_short | Rapid SARS-CoV-2 Detection Using Electrochemical Immunosensor |
title_sort | rapid sars-cov-2 detection using electrochemical immunosensor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827295/ https://www.ncbi.nlm.nih.gov/pubmed/33429915 http://dx.doi.org/10.3390/s21020390 |
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