Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein

Detalhes bibliográficos
Autor(a) principal: Bistaffa, Maria J. [UNESP]
Data de Publicação: 2022
Outros Autores: Camacho, Sabrina A. [UNESP], Pazin, Wallance M. [UNESP], Constantino, Carlos J.L. [UNESP], Oliveira, Osvaldo N., Aoki, Pedro H.B. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.talanta.2022.123381
http://hdl.handle.net/11449/234315
Resumo: The early diagnosis of Coronavirus disease (COVID-19) requires either an accurate detection of genetic material or a sensitive detection of viral proteins. In this work, we designed an immunoassay platform for detecting trace levels of SARS-CoV-2 spike (S) protein. It is based on surface-enhanced resonance Raman scattering (SERRS) of methylene blue (MB) adsorbed onto spherical gold nanoparticles (AuNPs) and coated with a 6 nm silica shell. The latter shell in the SERRS nanoprobe prevented aggregation and permitted functionalization with SARS-CoV-2 antibodies. Specificity of the immunoassay was achieved by combining this functionalization with antibody immobilization on the cover slides that served as the platform support. Different concentrations of SARS-CoV-2 antigen could be distinguished and the lack of influence of interferents was confirmed by treating SERRS data with the multidimensional projection technique Sammon's mapping. With SERRS using a laser line at 633 nm, the lowest concentration of spike protein detected was 10 pg/mL, achieving a limit of detection (LOD) of 0.046 ng/mL (0.60 pM). This value is comparable to the lowest concentrations in the plasma of COVID-19 patients at the onset of symptoms, thus indicating that the SERRS immunoassay platform may be employed for early diagnosis.
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spelling Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike proteinConjugation in gold nanoparticlesResonant Raman moleculesSARS-CoV-2 antibodiesSARS-CoV-2 spike protein detectionSERRS immunoassay PlatformSilica shell functionalizationThe early diagnosis of Coronavirus disease (COVID-19) requires either an accurate detection of genetic material or a sensitive detection of viral proteins. In this work, we designed an immunoassay platform for detecting trace levels of SARS-CoV-2 spike (S) protein. It is based on surface-enhanced resonance Raman scattering (SERRS) of methylene blue (MB) adsorbed onto spherical gold nanoparticles (AuNPs) and coated with a 6 nm silica shell. The latter shell in the SERRS nanoprobe prevented aggregation and permitted functionalization with SARS-CoV-2 antibodies. Specificity of the immunoassay was achieved by combining this functionalization with antibody immobilization on the cover slides that served as the platform support. Different concentrations of SARS-CoV-2 antigen could be distinguished and the lack of influence of interferents was confirmed by treating SERRS data with the multidimensional projection technique Sammon's mapping. With SERRS using a laser line at 633 nm, the lowest concentration of spike protein detected was 10 pg/mL, achieving a limit of detection (LOD) of 0.046 ng/mL (0.60 pM). This value is comparable to the lowest concentrations in the plasma of COVID-19 patients at the onset of symptoms, thus indicating that the SERRS immunoassay platform may be employed for early diagnosis.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Instituto Nacional de Ciência e Tecnologia em Eletrônica OrgânicaFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)São Paulo State University (UNESP) School of Sciences Humanities and Languages, Assis, SPIFSC São Carlos Institute of Physics University of São Paulo (USP), SPSão Paulo State University (UNESP) School of Technology and Applied Sciences, SPSão Paulo State University (UNESP) School of Sciences Humanities and Languages, Assis, SPSão Paulo State University (UNESP) School of Technology and Applied Sciences, SPFAPESP: 2018/14692–5FAPESP: 2018/16713–0FAPESP: 2018/22214–6FAPESP: 2020/12129–1CNPq: 403713/2016–1FAPESP: EMU 2017/03879–4FAPESP: FAPESPUniversidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Bistaffa, Maria J. [UNESP]Camacho, Sabrina A. [UNESP]Pazin, Wallance M. [UNESP]Constantino, Carlos J.L. [UNESP]Oliveira, Osvaldo N.Aoki, Pedro H.B. [UNESP]2022-05-01T15:46:20Z2022-05-01T15:46:20Z2022-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.talanta.2022.123381Talanta, v. 244.0039-9140http://hdl.handle.net/11449/23431510.1016/j.talanta.2022.1233812-s2.0-85127093023Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTalantainfo:eu-repo/semantics/openAccess2024-06-19T12:44:22Zoai:repositorio.unesp.br:11449/234315Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:29:10.418212Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
title Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
spellingShingle Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
Bistaffa, Maria J. [UNESP]
Conjugation in gold nanoparticles
Resonant Raman molecules
SARS-CoV-2 antibodies
SARS-CoV-2 spike protein detection
SERRS immunoassay Platform
Silica shell functionalization
title_short Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
title_full Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
title_fullStr Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
title_full_unstemmed Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
title_sort Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
author Bistaffa, Maria J. [UNESP]
author_facet Bistaffa, Maria J. [UNESP]
Camacho, Sabrina A. [UNESP]
Pazin, Wallance M. [UNESP]
Constantino, Carlos J.L. [UNESP]
Oliveira, Osvaldo N.
Aoki, Pedro H.B. [UNESP]
author_role author
author2 Camacho, Sabrina A. [UNESP]
Pazin, Wallance M. [UNESP]
Constantino, Carlos J.L. [UNESP]
Oliveira, Osvaldo N.
Aoki, Pedro H.B. [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Bistaffa, Maria J. [UNESP]
Camacho, Sabrina A. [UNESP]
Pazin, Wallance M. [UNESP]
Constantino, Carlos J.L. [UNESP]
Oliveira, Osvaldo N.
Aoki, Pedro H.B. [UNESP]
dc.subject.por.fl_str_mv Conjugation in gold nanoparticles
Resonant Raman molecules
SARS-CoV-2 antibodies
SARS-CoV-2 spike protein detection
SERRS immunoassay Platform
Silica shell functionalization
topic Conjugation in gold nanoparticles
Resonant Raman molecules
SARS-CoV-2 antibodies
SARS-CoV-2 spike protein detection
SERRS immunoassay Platform
Silica shell functionalization
description The early diagnosis of Coronavirus disease (COVID-19) requires either an accurate detection of genetic material or a sensitive detection of viral proteins. In this work, we designed an immunoassay platform for detecting trace levels of SARS-CoV-2 spike (S) protein. It is based on surface-enhanced resonance Raman scattering (SERRS) of methylene blue (MB) adsorbed onto spherical gold nanoparticles (AuNPs) and coated with a 6 nm silica shell. The latter shell in the SERRS nanoprobe prevented aggregation and permitted functionalization with SARS-CoV-2 antibodies. Specificity of the immunoassay was achieved by combining this functionalization with antibody immobilization on the cover slides that served as the platform support. Different concentrations of SARS-CoV-2 antigen could be distinguished and the lack of influence of interferents was confirmed by treating SERRS data with the multidimensional projection technique Sammon's mapping. With SERRS using a laser line at 633 nm, the lowest concentration of spike protein detected was 10 pg/mL, achieving a limit of detection (LOD) of 0.046 ng/mL (0.60 pM). This value is comparable to the lowest concentrations in the plasma of COVID-19 patients at the onset of symptoms, thus indicating that the SERRS immunoassay platform may be employed for early diagnosis.
publishDate 2022
dc.date.none.fl_str_mv 2022-05-01T15:46:20Z
2022-05-01T15:46:20Z
2022-07-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.talanta.2022.123381
Talanta, v. 244.
0039-9140
http://hdl.handle.net/11449/234315
10.1016/j.talanta.2022.123381
2-s2.0-85127093023
url http://dx.doi.org/10.1016/j.talanta.2022.123381
http://hdl.handle.net/11449/234315
identifier_str_mv Talanta, v. 244.
0039-9140
10.1016/j.talanta.2022.123381
2-s2.0-85127093023
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Talanta
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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