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A rapid cell-free expression and screening platform for antibody discovery

Antibody discovery is bottlenecked by the individual expression and evaluation of antigen-specific hits. Here, we address this bottleneck by developing a workflow combining cell-free DNA template generation, cell-free protein synthesis, and binding measurements of antibody fragments in a process tha...

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Autores principales: Hunt, Andrew C., Vögeli, Bastian, Hassan, Ahmed O., Guerrero, Laura, Kightlinger, Weston, Yoesep, Danielle J., Krüger, Antje, DeWinter, Madison, Diamond, Michael S., Karim, Ashty S., Jewett, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318062/
https://www.ncbi.nlm.nih.gov/pubmed/37400446
http://dx.doi.org/10.1038/s41467-023-38965-w
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author Hunt, Andrew C.
Vögeli, Bastian
Hassan, Ahmed O.
Guerrero, Laura
Kightlinger, Weston
Yoesep, Danielle J.
Krüger, Antje
DeWinter, Madison
Diamond, Michael S.
Karim, Ashty S.
Jewett, Michael C.
author_facet Hunt, Andrew C.
Vögeli, Bastian
Hassan, Ahmed O.
Guerrero, Laura
Kightlinger, Weston
Yoesep, Danielle J.
Krüger, Antje
DeWinter, Madison
Diamond, Michael S.
Karim, Ashty S.
Jewett, Michael C.
author_sort Hunt, Andrew C.
collection PubMed
description Antibody discovery is bottlenecked by the individual expression and evaluation of antigen-specific hits. Here, we address this bottleneck by developing a workflow combining cell-free DNA template generation, cell-free protein synthesis, and binding measurements of antibody fragments in a process that takes hours rather than weeks. We apply this workflow to evaluate 135 previously published antibodies targeting the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), including all 8 antibodies previously granted emergency use authorization for coronavirus disease 2019 (COVID-19), and demonstrate identification of the most potent antibodies. We also evaluate 119 anti-SARS-CoV-2 antibodies from a mouse immunized with the SARS-CoV-2 spike protein and identify neutralizing antibody candidates, including the antibody SC2-3, which binds the SARS-CoV-2 spike protein of all tested variants of concern. We expect that our cell-free workflow will accelerate the discovery and characterization of antibodies for future pandemics and for research, diagnostic, and therapeutic applications more broadly.
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spelling pubmed-103180622023-07-05 A rapid cell-free expression and screening platform for antibody discovery Hunt, Andrew C. Vögeli, Bastian Hassan, Ahmed O. Guerrero, Laura Kightlinger, Weston Yoesep, Danielle J. Krüger, Antje DeWinter, Madison Diamond, Michael S. Karim, Ashty S. Jewett, Michael C. Nat Commun Article Antibody discovery is bottlenecked by the individual expression and evaluation of antigen-specific hits. Here, we address this bottleneck by developing a workflow combining cell-free DNA template generation, cell-free protein synthesis, and binding measurements of antibody fragments in a process that takes hours rather than weeks. We apply this workflow to evaluate 135 previously published antibodies targeting the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), including all 8 antibodies previously granted emergency use authorization for coronavirus disease 2019 (COVID-19), and demonstrate identification of the most potent antibodies. We also evaluate 119 anti-SARS-CoV-2 antibodies from a mouse immunized with the SARS-CoV-2 spike protein and identify neutralizing antibody candidates, including the antibody SC2-3, which binds the SARS-CoV-2 spike protein of all tested variants of concern. We expect that our cell-free workflow will accelerate the discovery and characterization of antibodies for future pandemics and for research, diagnostic, and therapeutic applications more broadly. Nature Publishing Group UK 2023-07-03 /pmc/articles/PMC10318062/ /pubmed/37400446 http://dx.doi.org/10.1038/s41467-023-38965-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hunt, Andrew C.
Vögeli, Bastian
Hassan, Ahmed O.
Guerrero, Laura
Kightlinger, Weston
Yoesep, Danielle J.
Krüger, Antje
DeWinter, Madison
Diamond, Michael S.
Karim, Ashty S.
Jewett, Michael C.
A rapid cell-free expression and screening platform for antibody discovery
title A rapid cell-free expression and screening platform for antibody discovery
title_full A rapid cell-free expression and screening platform for antibody discovery
title_fullStr A rapid cell-free expression and screening platform for antibody discovery
title_full_unstemmed A rapid cell-free expression and screening platform for antibody discovery
title_short A rapid cell-free expression and screening platform for antibody discovery
title_sort rapid cell-free expression and screening platform for antibody discovery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318062/
https://www.ncbi.nlm.nih.gov/pubmed/37400446
http://dx.doi.org/10.1038/s41467-023-38965-w
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