Immunoassay platform with surface-enhanced resonance Raman scattering for detecting trace levels of SARS-CoV-2 spike protein
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , |
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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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 |
|
_version_ |
1808128519106985984 |