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A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein
Simple, timely, and precise detection of SARS-CoV-2 in clinical samples and contaminated surfaces aids in lowering attendant morbidity/mortality related to this infectious virus. Currently applied diagnostic techniques depend on a timely laboratory report following PCR testing. However, the applicat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024885/ https://www.ncbi.nlm.nih.gov/pubmed/35448292 http://dx.doi.org/10.3390/bios12040232 |
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author | Alhadrami, Hani A. Suaifan, Ghadeer A. R. Y. Zourob, Mohammed M. |
author_facet | Alhadrami, Hani A. Suaifan, Ghadeer A. R. Y. Zourob, Mohammed M. |
author_sort | Alhadrami, Hani A. |
collection | PubMed |
description | Simple, timely, and precise detection of SARS-CoV-2 in clinical samples and contaminated surfaces aids in lowering attendant morbidity/mortality related to this infectious virus. Currently applied diagnostic techniques depend on a timely laboratory report following PCR testing. However, the application of these tests is associated with inherent shortcomings due to the need for trained personnel, long-time centralized laboratories, and expensive instruments. Therefore, there is an interest in developing biosensing diagnostic frontiers that can help in eliminating these shortcomings with a relatively economical, easy-to-use, well-timed, precise and sensitive technology. This study reports the development of fabricated Q-tips designed to qualitatively and semi-quantitatively detect SARS-CoV-2 in clinical samples and contaminated non-absorbable surfaces. This colorimetric sensor is engineered to sandwich SARS-CoV-2 spike protein between the lactoferrin general capturing agent and the complementary ACE2-labeled receptor. The ACE2 receptor is decorated with an orange-colored polymeric nanoparticle to generate an optical visual signal upon pairing with the SARS-CoV-2 spike protein. This colorimetric change of the Q-tip testing zone from white to orange confirms a positive result. The visual detection limit of the COVID-19 engineered colorimetric Q-tip sensor was 100 pfu/mL within a relatively short turnaround time of 5 min. The linear working range of quantitation was 10(3)–10(8) pfu/mL. The engineered sensor selectively targeted SARS-CoV-2 spike protein and did not bind to another coronavirus such as MERS-CoV, Flu A, or Flu B present on the contaminated surface. This novel detection tool is relatively cheap to produce and suitable for onsite detection of COVID-19 infection. |
format | Online Article Text |
id | pubmed-9024885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90248852022-04-23 A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein Alhadrami, Hani A. Suaifan, Ghadeer A. R. Y. Zourob, Mohammed M. Biosensors (Basel) Article Simple, timely, and precise detection of SARS-CoV-2 in clinical samples and contaminated surfaces aids in lowering attendant morbidity/mortality related to this infectious virus. Currently applied diagnostic techniques depend on a timely laboratory report following PCR testing. However, the application of these tests is associated with inherent shortcomings due to the need for trained personnel, long-time centralized laboratories, and expensive instruments. Therefore, there is an interest in developing biosensing diagnostic frontiers that can help in eliminating these shortcomings with a relatively economical, easy-to-use, well-timed, precise and sensitive technology. This study reports the development of fabricated Q-tips designed to qualitatively and semi-quantitatively detect SARS-CoV-2 in clinical samples and contaminated non-absorbable surfaces. This colorimetric sensor is engineered to sandwich SARS-CoV-2 spike protein between the lactoferrin general capturing agent and the complementary ACE2-labeled receptor. The ACE2 receptor is decorated with an orange-colored polymeric nanoparticle to generate an optical visual signal upon pairing with the SARS-CoV-2 spike protein. This colorimetric change of the Q-tip testing zone from white to orange confirms a positive result. The visual detection limit of the COVID-19 engineered colorimetric Q-tip sensor was 100 pfu/mL within a relatively short turnaround time of 5 min. The linear working range of quantitation was 10(3)–10(8) pfu/mL. The engineered sensor selectively targeted SARS-CoV-2 spike protein and did not bind to another coronavirus such as MERS-CoV, Flu A, or Flu B present on the contaminated surface. This novel detection tool is relatively cheap to produce and suitable for onsite detection of COVID-19 infection. MDPI 2022-04-11 /pmc/articles/PMC9024885/ /pubmed/35448292 http://dx.doi.org/10.3390/bios12040232 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alhadrami, Hani A. Suaifan, Ghadeer A. R. Y. Zourob, Mohammed M. A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein |
title | A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein |
title_full | A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein |
title_fullStr | A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein |
title_full_unstemmed | A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein |
title_short | A Portable Nanoprobe for Rapid and Sensitive Detection of SARS-CoV-2 S1 Protein |
title_sort | portable nanoprobe for rapid and sensitive detection of sars-cov-2 s1 protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024885/ https://www.ncbi.nlm.nih.gov/pubmed/35448292 http://dx.doi.org/10.3390/bios12040232 |
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