Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2

Autores
He, Yawen; Xu, Zhiyuan; Kasputis, Tom; Zhao, Xue; Ibañez, Itati; Pavan, Florencia; Bok, Marina; Malito, Juan Pablo; Parreño, Gladys Viviana; Yuan, Lijuan; Wright, R. Clay; Chen, Juhong
Año de publicación
2023
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The accurate and effective detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is essential to preventing the spread of infectious diseases and ensuring human health. Herein, a nanobody-displayed whole-cell biosensor was developed for colorimetric detection of SARS-CoV-2 spike proteins. Serving as bioreceptors, yeast surfaces were genetically engineered to display SARS-CoV-2 binding of llama-derived single-domain antibodies (nanobodies) with high capture efficiency, facilitating the concentration and purification of SARS-CoV-2. Gold nanoparticles (AuNPs) employed as signal transductions were functionalized with horseradish peroxidase (HRP) and anti-SARS monoclonal antibodies to enhance the detection sensitivity. In the presence of SARS-CoV-2 spike proteins, the sandwiched binding will be formed by linking engineered yeast, SARS-CoV-2 spike proteins, and reporter AuNPs. The colorimetric signal was generated by the enzymatic reaction of HRP and its corresponding colorimetric substrate/chromogen system. At the optimal conditions, the developed whole-cell biosensor enables the sensitive detection of SARS-CoV-2 spike proteins in a linear range from 0.01 to 1 μg/mL with a limit of detection (LOD) of 0.037 μg/mL (about 4 × 108 virion particles/mL). Furthermore, the whole-cell biosensor was demonstrated to detect the spike protein of different SARS-CoV-2 variants in human serum, providing new possibilities for the detection of future SARS-CoV-2 variants.
Instituto de Virología
Fil: He, Yawen. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Xu, Zhiyuan. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Kasputis, Tom. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Zhao, Xue. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Ibañez, Itati. Universidad de Buenos Aires. Instituto de Química Física de los Materiales, Medio Ambiente y Energía (INQUIMAE); Argentina
Fil: Ibañez, Itati. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Pavan, Florencia. Universidad de Buenos Aires. Instituto de Química Física de los Materiales, Medio Ambiente y Energía (INQUIMAE); Argentina
Fil: Pavan, Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Bok, Marina. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virología e Innovaciones Tecnologicas; Argentina
Fil: Bok, Marina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Malito, Juan Pablo. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virología e Innovaciones Tecnologicas; Argentina
Fil: Malito, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Parreño, Gladys Viviana. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virologia e Innovaciones Tecnologicas (IVIT); Argentina
Fil: Parreño, Gladys Viviana. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Parreño, Gladys Viviana. Virginia-Maryland College of Veterinary Medicine. Department of Biomedical Sciences and Pathobiology; Estados Unidos
Fil: Yuan, Lijuan. Virginia-Maryland College of Veterinary Medicine. Department of Biomedical Sciences and Pathobiology; Estados Unidos
Fil: Wright, R. Clay. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Chen, Juhong. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fuente
ACS Applied Materials & Interfaces 15 : 37184-37192 (Agosto 2023)
Materia
Biosensors
Colorimetry
Severe Acute Respiratory Syndrome Coronavirus 2
Biosensores
Colorimetría
Coronavirus del Síndrome Respiratorio Agudo Grave 2
Nanobody
Nanocuerpo
SARS-CoV-2
Nivel de accesibilidad
acceso restringido
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
INTA Digital (INTA)
Institución
Instituto Nacional de Tecnología Agropecuaria
OAI Identificador
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spelling Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2He, YawenXu, ZhiyuanKasputis, TomZhao, XueIbañez, ItatiPavan, FlorenciaBok, MarinaMalito, Juan PabloParreño, Gladys VivianaYuan, LijuanWright, R. ClayChen, JuhongBiosensorsColorimetrySevere Acute Respiratory Syndrome Coronavirus 2BiosensoresColorimetríaCoronavirus del Síndrome Respiratorio Agudo Grave 2NanobodyNanocuerpoSARS-CoV-2The accurate and effective detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is essential to preventing the spread of infectious diseases and ensuring human health. Herein, a nanobody-displayed whole-cell biosensor was developed for colorimetric detection of SARS-CoV-2 spike proteins. Serving as bioreceptors, yeast surfaces were genetically engineered to display SARS-CoV-2 binding of llama-derived single-domain antibodies (nanobodies) with high capture efficiency, facilitating the concentration and purification of SARS-CoV-2. Gold nanoparticles (AuNPs) employed as signal transductions were functionalized with horseradish peroxidase (HRP) and anti-SARS monoclonal antibodies to enhance the detection sensitivity. In the presence of SARS-CoV-2 spike proteins, the sandwiched binding will be formed by linking engineered yeast, SARS-CoV-2 spike proteins, and reporter AuNPs. The colorimetric signal was generated by the enzymatic reaction of HRP and its corresponding colorimetric substrate/chromogen system. At the optimal conditions, the developed whole-cell biosensor enables the sensitive detection of SARS-CoV-2 spike proteins in a linear range from 0.01 to 1 μg/mL with a limit of detection (LOD) of 0.037 μg/mL (about 4 × 108 virion particles/mL). Furthermore, the whole-cell biosensor was demonstrated to detect the spike protein of different SARS-CoV-2 variants in human serum, providing new possibilities for the detection of future SARS-CoV-2 variants.Instituto de VirologíaFil: He, Yawen. Virginia Tech. Department of Biological Systems Engineering; Estados UnidosFil: Xu, Zhiyuan. Virginia Tech. Department of Biological Systems Engineering; Estados UnidosFil: Kasputis, Tom. Virginia Tech. Department of Biological Systems Engineering; Estados UnidosFil: Zhao, Xue. Virginia Tech. Department of Biological Systems Engineering; Estados UnidosFil: Ibañez, Itati. Universidad de Buenos Aires. Instituto de Química Física de los Materiales, Medio Ambiente y Energía (INQUIMAE); ArgentinaFil: Ibañez, Itati. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Pavan, Florencia. Universidad de Buenos Aires. Instituto de Química Física de los Materiales, Medio Ambiente y Energía (INQUIMAE); ArgentinaFil: Pavan, Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Bok, Marina. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virología e Innovaciones Tecnologicas; ArgentinaFil: Bok, Marina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Malito, Juan Pablo. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virología e Innovaciones Tecnologicas; ArgentinaFil: Malito, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Parreño, Gladys Viviana. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virologia e Innovaciones Tecnologicas (IVIT); ArgentinaFil: Parreño, Gladys Viviana. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Parreño, Gladys Viviana. Virginia-Maryland College of Veterinary Medicine. Department of Biomedical Sciences and Pathobiology; Estados UnidosFil: Yuan, Lijuan. Virginia-Maryland College of Veterinary Medicine. Department of Biomedical Sciences and Pathobiology; Estados UnidosFil: Wright, R. Clay. Virginia Tech. Department of Biological Systems Engineering; Estados UnidosFil: Chen, Juhong. Virginia Tech. Department of Biological Systems Engineering; Estados UnidosAmerican Chemical Society2023-09-15T10:55:41Z2023-09-15T10:55:41Z2023-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12123/15222https://pubs.acs.org/doi/10.1021/acsami.3c059001944-8252https://doi.org/10.1021/acsami.3c05900ACS Applied Materials & Interfaces 15 : 37184-37192 (Agosto 2023)reponame:INTA Digital (INTA)instname:Instituto Nacional de Tecnología Agropecuariaenginfo:eu-repo/semantics/restrictedAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)2025-09-04T09:49:56Zoai:localhost:20.500.12123/15222instacron:INTAInstitucionalhttp://repositorio.inta.gob.ar/Organismo científico-tecnológicoNo correspondehttp://repositorio.inta.gob.ar/oai/requesttripaldi.nicolas@inta.gob.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:l2025-09-04 09:49:57.346INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuariafalse
dc.title.none.fl_str_mv Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
title Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
spellingShingle Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
He, Yawen
Biosensors
Colorimetry
Severe Acute Respiratory Syndrome Coronavirus 2
Biosensores
Colorimetría
Coronavirus del Síndrome Respiratorio Agudo Grave 2
Nanobody
Nanocuerpo
SARS-CoV-2
title_short Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
title_full Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
title_fullStr Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
title_full_unstemmed Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
title_sort Development of nanobody-displayed whole-cell biosensors for the colorimetric detection of SARS-CoV‑2
dc.creator.none.fl_str_mv He, Yawen
Xu, Zhiyuan
Kasputis, Tom
Zhao, Xue
Ibañez, Itati
Pavan, Florencia
Bok, Marina
Malito, Juan Pablo
Parreño, Gladys Viviana
Yuan, Lijuan
Wright, R. Clay
Chen, Juhong
author He, Yawen
author_facet He, Yawen
Xu, Zhiyuan
Kasputis, Tom
Zhao, Xue
Ibañez, Itati
Pavan, Florencia
Bok, Marina
Malito, Juan Pablo
Parreño, Gladys Viviana
Yuan, Lijuan
Wright, R. Clay
Chen, Juhong
author_role author
author2 Xu, Zhiyuan
Kasputis, Tom
Zhao, Xue
Ibañez, Itati
Pavan, Florencia
Bok, Marina
Malito, Juan Pablo
Parreño, Gladys Viviana
Yuan, Lijuan
Wright, R. Clay
Chen, Juhong
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Biosensors
Colorimetry
Severe Acute Respiratory Syndrome Coronavirus 2
Biosensores
Colorimetría
Coronavirus del Síndrome Respiratorio Agudo Grave 2
Nanobody
Nanocuerpo
SARS-CoV-2
topic Biosensors
Colorimetry
Severe Acute Respiratory Syndrome Coronavirus 2
Biosensores
Colorimetría
Coronavirus del Síndrome Respiratorio Agudo Grave 2
Nanobody
Nanocuerpo
SARS-CoV-2
dc.description.none.fl_txt_mv The accurate and effective detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is essential to preventing the spread of infectious diseases and ensuring human health. Herein, a nanobody-displayed whole-cell biosensor was developed for colorimetric detection of SARS-CoV-2 spike proteins. Serving as bioreceptors, yeast surfaces were genetically engineered to display SARS-CoV-2 binding of llama-derived single-domain antibodies (nanobodies) with high capture efficiency, facilitating the concentration and purification of SARS-CoV-2. Gold nanoparticles (AuNPs) employed as signal transductions were functionalized with horseradish peroxidase (HRP) and anti-SARS monoclonal antibodies to enhance the detection sensitivity. In the presence of SARS-CoV-2 spike proteins, the sandwiched binding will be formed by linking engineered yeast, SARS-CoV-2 spike proteins, and reporter AuNPs. The colorimetric signal was generated by the enzymatic reaction of HRP and its corresponding colorimetric substrate/chromogen system. At the optimal conditions, the developed whole-cell biosensor enables the sensitive detection of SARS-CoV-2 spike proteins in a linear range from 0.01 to 1 μg/mL with a limit of detection (LOD) of 0.037 μg/mL (about 4 × 108 virion particles/mL). Furthermore, the whole-cell biosensor was demonstrated to detect the spike protein of different SARS-CoV-2 variants in human serum, providing new possibilities for the detection of future SARS-CoV-2 variants.
Instituto de Virología
Fil: He, Yawen. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Xu, Zhiyuan. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Kasputis, Tom. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Zhao, Xue. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Ibañez, Itati. Universidad de Buenos Aires. Instituto de Química Física de los Materiales, Medio Ambiente y Energía (INQUIMAE); Argentina
Fil: Ibañez, Itati. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Pavan, Florencia. Universidad de Buenos Aires. Instituto de Química Física de los Materiales, Medio Ambiente y Energía (INQUIMAE); Argentina
Fil: Pavan, Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Bok, Marina. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virología e Innovaciones Tecnologicas; Argentina
Fil: Bok, Marina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Malito, Juan Pablo. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virología e Innovaciones Tecnologicas; Argentina
Fil: Malito, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Parreño, Gladys Viviana. Instituto Nacional de Tecnología Agropecuaria (INTA). INCUINTA. Instituto de Virologia e Innovaciones Tecnologicas (IVIT); Argentina
Fil: Parreño, Gladys Viviana. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Parreño, Gladys Viviana. Virginia-Maryland College of Veterinary Medicine. Department of Biomedical Sciences and Pathobiology; Estados Unidos
Fil: Yuan, Lijuan. Virginia-Maryland College of Veterinary Medicine. Department of Biomedical Sciences and Pathobiology; Estados Unidos
Fil: Wright, R. Clay. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
Fil: Chen, Juhong. Virginia Tech. Department of Biological Systems Engineering; Estados Unidos
description The accurate and effective detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is essential to preventing the spread of infectious diseases and ensuring human health. Herein, a nanobody-displayed whole-cell biosensor was developed for colorimetric detection of SARS-CoV-2 spike proteins. Serving as bioreceptors, yeast surfaces were genetically engineered to display SARS-CoV-2 binding of llama-derived single-domain antibodies (nanobodies) with high capture efficiency, facilitating the concentration and purification of SARS-CoV-2. Gold nanoparticles (AuNPs) employed as signal transductions were functionalized with horseradish peroxidase (HRP) and anti-SARS monoclonal antibodies to enhance the detection sensitivity. In the presence of SARS-CoV-2 spike proteins, the sandwiched binding will be formed by linking engineered yeast, SARS-CoV-2 spike proteins, and reporter AuNPs. The colorimetric signal was generated by the enzymatic reaction of HRP and its corresponding colorimetric substrate/chromogen system. At the optimal conditions, the developed whole-cell biosensor enables the sensitive detection of SARS-CoV-2 spike proteins in a linear range from 0.01 to 1 μg/mL with a limit of detection (LOD) of 0.037 μg/mL (about 4 × 108 virion particles/mL). Furthermore, the whole-cell biosensor was demonstrated to detect the spike protein of different SARS-CoV-2 variants in human serum, providing new possibilities for the detection of future SARS-CoV-2 variants.
publishDate 2023
dc.date.none.fl_str_mv 2023-09-15T10:55:41Z
2023-09-15T10:55:41Z
2023-08
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12123/15222
https://pubs.acs.org/doi/10.1021/acsami.3c05900
1944-8252
https://doi.org/10.1021/acsami.3c05900
url http://hdl.handle.net/20.500.12123/15222
https://pubs.acs.org/doi/10.1021/acsami.3c05900
https://doi.org/10.1021/acsami.3c05900
identifier_str_mv 1944-8252
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/restrictedAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv restrictedAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv ACS Applied Materials & Interfaces 15 : 37184-37192 (Agosto 2023)
reponame:INTA Digital (INTA)
instname:Instituto Nacional de Tecnología Agropecuaria
reponame_str INTA Digital (INTA)
collection INTA Digital (INTA)
instname_str Instituto Nacional de Tecnología Agropecuaria
repository.name.fl_str_mv INTA Digital (INTA) - Instituto Nacional de Tecnología Agropecuaria
repository.mail.fl_str_mv tripaldi.nicolas@inta.gob.ar
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