Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1785067956198178816 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10318062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT huntandrewc arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT vogelibastian arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT hassanahmedo arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT guerrerolaura arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT kightlingerweston arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT yoesepdaniellej arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT krugerantje arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT dewintermadison arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT diamondmichaels arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT karimashtys arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT jewettmichaelc arapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT huntandrewc rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT vogelibastian rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT hassanahmedo rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT guerrerolaura rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT kightlingerweston rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT yoesepdaniellej rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT krugerantje rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT dewintermadison rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT diamondmichaels rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT karimashtys rapidcellfreeexpressionandscreeningplatformforantibodydiscovery AT jewettmichaelc rapidcellfreeexpressionandscreeningplatformforantibodydiscovery |