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Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry

Serological testing to evaluate antigen-specific antibodies in plasma is generally performed by rapid lateral flow test strips that lack quantitative results or by high complexity immunoassays that are time- and labor-intensive but provide semi-quantitative results. Here, we describe a novel applica...

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Autores principales: Dzimianski, John V., Lorig-Roach, Nicholas, O’Rourke, Sara M., Alexander, David L., Kimmey, Jacqueline M., DuBois, Rebecca M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730435/
https://www.ncbi.nlm.nih.gov/pubmed/33303951
http://dx.doi.org/10.1038/s41598-020-78895-x
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author Dzimianski, John V.
Lorig-Roach, Nicholas
O’Rourke, Sara M.
Alexander, David L.
Kimmey, Jacqueline M.
DuBois, Rebecca M.
author_facet Dzimianski, John V.
Lorig-Roach, Nicholas
O’Rourke, Sara M.
Alexander, David L.
Kimmey, Jacqueline M.
DuBois, Rebecca M.
author_sort Dzimianski, John V.
collection PubMed
description Serological testing to evaluate antigen-specific antibodies in plasma is generally performed by rapid lateral flow test strips that lack quantitative results or by high complexity immunoassays that are time- and labor-intensive but provide semi-quantitative results. Here, we describe a novel application of biolayer interferometry for the rapid detection of antigen-specific antibody levels in plasma samples, and demonstrate its utility for quantification of SARS-CoV-2 antibodies. Our biolayer interferometry immunosorbent assay (BLI-ISA) utilizes single-use biosensors in an automated “dip-and-read” format, providing real-time optical measurements of antigen loading, plasma antibody binding, and antibody isotype detection. Complete semi-quantitative results are obtained in less than 20 min. BLI-ISA meets or exceeds the performance of high complexity methods such as Enzyme-Linked Immunosorbent Assay (ELISA) and Chemiluminescent Immunoassay. Importantly, our method can be immediately implemented on existing BLI platforms for urgent COVID-19 studies, such as serosurveillance and the evaluation of vaccine candidates. In a broader sense, BLI-ISA can be developed as a novel diagnostic platform to evaluate antibodies and other biomolecules in clinical specimens.
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spelling pubmed-77304352020-12-14 Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry Dzimianski, John V. Lorig-Roach, Nicholas O’Rourke, Sara M. Alexander, David L. Kimmey, Jacqueline M. DuBois, Rebecca M. Sci Rep Article Serological testing to evaluate antigen-specific antibodies in plasma is generally performed by rapid lateral flow test strips that lack quantitative results or by high complexity immunoassays that are time- and labor-intensive but provide semi-quantitative results. Here, we describe a novel application of biolayer interferometry for the rapid detection of antigen-specific antibody levels in plasma samples, and demonstrate its utility for quantification of SARS-CoV-2 antibodies. Our biolayer interferometry immunosorbent assay (BLI-ISA) utilizes single-use biosensors in an automated “dip-and-read” format, providing real-time optical measurements of antigen loading, plasma antibody binding, and antibody isotype detection. Complete semi-quantitative results are obtained in less than 20 min. BLI-ISA meets or exceeds the performance of high complexity methods such as Enzyme-Linked Immunosorbent Assay (ELISA) and Chemiluminescent Immunoassay. Importantly, our method can be immediately implemented on existing BLI platforms for urgent COVID-19 studies, such as serosurveillance and the evaluation of vaccine candidates. In a broader sense, BLI-ISA can be developed as a novel diagnostic platform to evaluate antibodies and other biomolecules in clinical specimens. Nature Publishing Group UK 2020-12-10 /pmc/articles/PMC7730435/ /pubmed/33303951 http://dx.doi.org/10.1038/s41598-020-78895-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dzimianski, John V.
Lorig-Roach, Nicholas
O’Rourke, Sara M.
Alexander, David L.
Kimmey, Jacqueline M.
DuBois, Rebecca M.
Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry
title Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry
title_full Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry
title_fullStr Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry
title_full_unstemmed Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry
title_short Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry
title_sort rapid and sensitive detection of sars-cov-2 antibodies by biolayer interferometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730435/
https://www.ncbi.nlm.nih.gov/pubmed/33303951
http://dx.doi.org/10.1038/s41598-020-78895-x
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