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Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants

Epidemiological control and public health monitoring during the outbreaks of infectious viral diseases rely on the ability to detect viral pathogens. Here we demonstrate a rapid, sensitive, and selective nanotechnology-enhanced severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection b...

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Autores principales: Yeh, Yi-Jui, Le, Trong-Nghia, Hsiao, Wesley Wei-Wen, Tung, Kuo-Lun, Ostrikov, Kostya (Ken), Chiang, Wei-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677586/
https://www.ncbi.nlm.nih.gov/pubmed/36628748
http://dx.doi.org/10.1016/j.aca.2022.340651
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author Yeh, Yi-Jui
Le, Trong-Nghia
Hsiao, Wesley Wei-Wen
Tung, Kuo-Lun
Ostrikov, Kostya (Ken)
Chiang, Wei-Hung
author_facet Yeh, Yi-Jui
Le, Trong-Nghia
Hsiao, Wesley Wei-Wen
Tung, Kuo-Lun
Ostrikov, Kostya (Ken)
Chiang, Wei-Hung
author_sort Yeh, Yi-Jui
collection PubMed
description Epidemiological control and public health monitoring during the outbreaks of infectious viral diseases rely on the ability to detect viral pathogens. Here we demonstrate a rapid, sensitive, and selective nanotechnology-enhanced severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection based on the surface-enhanced Raman scattering (SERS) responses from the plasma-engineered, variant-specific antibody-functionalized silver microplasma-engineered nanoassemblies (AgMEN) interacting with the SARS-CoV-2 spike (S) and nucleocapsid (N) proteins. The three-dimensional (3D) porous AgMEN with plasmonic-active nanostructures provide a high sensitivity to virus detection via the remarkable SERS signal collection. Moreover, the variant-specific antibody-functionalization on the SERS-active AgMEN enabled the high selectivity of the SARS-CoV-2 S variants, including wild-type, Alpha, Delta, and Omicron, under the simulated human saliva conditions. The exceptional ultrahigh sensitivity of our SERS biosensor was demonstrated via SARS-CoV-2 S and N proteins at the detection limit of 1 fg mL(−1) and 0.1 pg mL(−1), respectively. Our work demonstrates a versatile SERS-based detection platform can be applied for the ultrasensitive detection of virus variants, infectious diseases, and cancer biomarkers.
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spelling pubmed-96775862022-11-21 Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants Yeh, Yi-Jui Le, Trong-Nghia Hsiao, Wesley Wei-Wen Tung, Kuo-Lun Ostrikov, Kostya (Ken) Chiang, Wei-Hung Anal Chim Acta Article Epidemiological control and public health monitoring during the outbreaks of infectious viral diseases rely on the ability to detect viral pathogens. Here we demonstrate a rapid, sensitive, and selective nanotechnology-enhanced severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection based on the surface-enhanced Raman scattering (SERS) responses from the plasma-engineered, variant-specific antibody-functionalized silver microplasma-engineered nanoassemblies (AgMEN) interacting with the SARS-CoV-2 spike (S) and nucleocapsid (N) proteins. The three-dimensional (3D) porous AgMEN with plasmonic-active nanostructures provide a high sensitivity to virus detection via the remarkable SERS signal collection. Moreover, the variant-specific antibody-functionalization on the SERS-active AgMEN enabled the high selectivity of the SARS-CoV-2 S variants, including wild-type, Alpha, Delta, and Omicron, under the simulated human saliva conditions. The exceptional ultrahigh sensitivity of our SERS biosensor was demonstrated via SARS-CoV-2 S and N proteins at the detection limit of 1 fg mL(−1) and 0.1 pg mL(−1), respectively. Our work demonstrates a versatile SERS-based detection platform can be applied for the ultrasensitive detection of virus variants, infectious diseases, and cancer biomarkers. Elsevier B.V. 2023-01-25 2022-11-21 /pmc/articles/PMC9677586/ /pubmed/36628748 http://dx.doi.org/10.1016/j.aca.2022.340651 Text en © 2022 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
Yeh, Yi-Jui
Le, Trong-Nghia
Hsiao, Wesley Wei-Wen
Tung, Kuo-Lun
Ostrikov, Kostya (Ken)
Chiang, Wei-Hung
Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants
title Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants
title_full Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants
title_fullStr Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants
title_full_unstemmed Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants
title_short Plasmonic nanostructure-enhanced Raman scattering for detection of SARS-CoV-2 nucleocapsid protein and spike protein variants
title_sort plasmonic nanostructure-enhanced raman scattering for detection of sars-cov-2 nucleocapsid protein and spike protein variants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677586/
https://www.ncbi.nlm.nih.gov/pubmed/36628748
http://dx.doi.org/10.1016/j.aca.2022.340651
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