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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 quantitative results. Here, we describe a novel application...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388487/ https://www.ncbi.nlm.nih.gov/pubmed/32743612 http://dx.doi.org/10.1101/2020.07.17.20156281 |
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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 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 quantitative results are obtained in less than 20 minutes. 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. |
format | Online Article Text |
id | pubmed-7388487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-73884872020-07-31 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. medRxiv 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 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 quantitative results are obtained in less than 20 minutes. 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. Cold Spring Harbor Laboratory 2020-07-19 /pmc/articles/PMC7388487/ /pubmed/32743612 http://dx.doi.org/10.1101/2020.07.17.20156281 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY-NC-ND 4.0 International license (https://creativecommons.org/licenses/by-nc-nd/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/PMC7388487/ https://www.ncbi.nlm.nih.gov/pubmed/32743612 http://dx.doi.org/10.1101/2020.07.17.20156281 |
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