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A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples

The ongoing coronavirus disease 2019 (COVID-19) pandemic continues to threaten public health systems all around the world. In controlling the viral outbreak, early diagnosis of COVID-19 is pivotal. This article describes a novel method of voltammetrically determining severe acute respiratory syndrom...

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Detalles Bibliográficos
Autores principales: Liv, Lokman, Çoban, Gizem, Nakiboğlu, Nuri, Kocagöz, Tanıl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8276568/
https://www.ncbi.nlm.nih.gov/pubmed/34274624
http://dx.doi.org/10.1016/j.bios.2021.113497
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author Liv, Lokman
Çoban, Gizem
Nakiboğlu, Nuri
Kocagöz, Tanıl
author_facet Liv, Lokman
Çoban, Gizem
Nakiboğlu, Nuri
Kocagöz, Tanıl
author_sort Liv, Lokman
collection PubMed
description The ongoing coronavirus disease 2019 (COVID-19) pandemic continues to threaten public health systems all around the world. In controlling the viral outbreak, early diagnosis of COVID-19 is pivotal. This article describes a novel method of voltammetrically determining severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein with a newly designed sensor involving bovine serum albumin, SARS-CoV-2 spike antibody and a functionalised graphene oxide modified glassy carbon electrode (BSA/AB/f-GO/GCE) or screen-printed electrode (BSA/AB/f-GO/SPE). The oxidation reaction based on the antibody–antigen protein interaction was evaluated as a response to SARS-CoV-2 spike protein at -200 mV and 1430 mV with the BSA/AB/f-GO/SPE and BSA/AB/f-GO/GCE, respectively. The developed sensors, BSA/AB/f-GO/SPE and BSA/AB/f-GO/GCE, could detect 1 ag/mL of virus spike protein in synthetic, saliva and oropharyngeal swab samples in 5 min and 35 min, and both sensors demonstrated a dynamic response to the SARS-CoV-2 spike protein between 1 ag/mL and 10 fg/mL. Real-time polymerase chain reaction (RT-PCR), rapid antigen test and the proposed method were applied to saliva samples. When compared to RT-PCR, it was observed that the developed method had a 92.5% specificity and 93.3% sensitivity. Moreover, BSA/AB/f-GO/SPE sensor achieved 91.7% accuracy compared to 66.7% accuracy of rapid antigen test kit in positive samples. In view of these findings, the developed sensor provides great potential for the diagnosing of COVID-19 in real samples.
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spelling pubmed-82765682021-07-14 A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples Liv, Lokman Çoban, Gizem Nakiboğlu, Nuri Kocagöz, Tanıl Biosens Bioelectron Article The ongoing coronavirus disease 2019 (COVID-19) pandemic continues to threaten public health systems all around the world. In controlling the viral outbreak, early diagnosis of COVID-19 is pivotal. This article describes a novel method of voltammetrically determining severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein with a newly designed sensor involving bovine serum albumin, SARS-CoV-2 spike antibody and a functionalised graphene oxide modified glassy carbon electrode (BSA/AB/f-GO/GCE) or screen-printed electrode (BSA/AB/f-GO/SPE). The oxidation reaction based on the antibody–antigen protein interaction was evaluated as a response to SARS-CoV-2 spike protein at -200 mV and 1430 mV with the BSA/AB/f-GO/SPE and BSA/AB/f-GO/GCE, respectively. The developed sensors, BSA/AB/f-GO/SPE and BSA/AB/f-GO/GCE, could detect 1 ag/mL of virus spike protein in synthetic, saliva and oropharyngeal swab samples in 5 min and 35 min, and both sensors demonstrated a dynamic response to the SARS-CoV-2 spike protein between 1 ag/mL and 10 fg/mL. Real-time polymerase chain reaction (RT-PCR), rapid antigen test and the proposed method were applied to saliva samples. When compared to RT-PCR, it was observed that the developed method had a 92.5% specificity and 93.3% sensitivity. Moreover, BSA/AB/f-GO/SPE sensor achieved 91.7% accuracy compared to 66.7% accuracy of rapid antigen test kit in positive samples. In view of these findings, the developed sensor provides great potential for the diagnosing of COVID-19 in real samples. Elsevier B.V. 2021-11-15 2021-07-13 /pmc/articles/PMC8276568/ /pubmed/34274624 http://dx.doi.org/10.1016/j.bios.2021.113497 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
Liv, Lokman
Çoban, Gizem
Nakiboğlu, Nuri
Kocagöz, Tanıl
A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples
title A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples
title_full A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples
title_fullStr A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples
title_full_unstemmed A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples
title_short A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples
title_sort rapid, ultrasensitive voltammetric biosensor for determining sars-cov-2 spike protein in real samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8276568/
https://www.ncbi.nlm.nih.gov/pubmed/34274624
http://dx.doi.org/10.1016/j.bios.2021.113497
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