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Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis

The generation of high-affinity nanobodies for diverse biomedical applications typically requires immunization or affinity maturation. Here, we report a simple protocol using complementarity-determining region (CDR)-swapping mutagenesis to isolate high-affinity nanobodies from common framework libra...

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Detalles Bibliográficos
Autores principales: Zupancic, Jennifer M., Desai, Alec A., Tessier, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8783142/
https://www.ncbi.nlm.nih.gov/pubmed/35098159
http://dx.doi.org/10.1016/j.xpro.2021.101101
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author Zupancic, Jennifer M.
Desai, Alec A.
Tessier, Peter M.
author_facet Zupancic, Jennifer M.
Desai, Alec A.
Tessier, Peter M.
author_sort Zupancic, Jennifer M.
collection PubMed
description The generation of high-affinity nanobodies for diverse biomedical applications typically requires immunization or affinity maturation. Here, we report a simple protocol using complementarity-determining region (CDR)-swapping mutagenesis to isolate high-affinity nanobodies from common framework libraries. This approach involves shuffling the CDRs of low-affinity variants during the sorting of yeast-displayed libraries to directly isolate high-affinity nanobodies without the need for lead isolation and optimization. We expect this approach, which we demonstrate for SARS-CoV-2 neutralizing nanobodies, will simplify the generation of high-affinity nanobodies. For complete details on the use and execution of this profile, please refer to Zupancic et al. (2021).
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spelling pubmed-87831422022-01-28 Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis Zupancic, Jennifer M. Desai, Alec A. Tessier, Peter M. STAR Protoc Protocol The generation of high-affinity nanobodies for diverse biomedical applications typically requires immunization or affinity maturation. Here, we report a simple protocol using complementarity-determining region (CDR)-swapping mutagenesis to isolate high-affinity nanobodies from common framework libraries. This approach involves shuffling the CDRs of low-affinity variants during the sorting of yeast-displayed libraries to directly isolate high-affinity nanobodies without the need for lead isolation and optimization. We expect this approach, which we demonstrate for SARS-CoV-2 neutralizing nanobodies, will simplify the generation of high-affinity nanobodies. For complete details on the use and execution of this profile, please refer to Zupancic et al. (2021). Elsevier 2022-01-20 /pmc/articles/PMC8783142/ /pubmed/35098159 http://dx.doi.org/10.1016/j.xpro.2021.101101 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Zupancic, Jennifer M.
Desai, Alec A.
Tessier, Peter M.
Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis
title Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis
title_full Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis
title_fullStr Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis
title_full_unstemmed Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis
title_short Facile isolation of high-affinity nanobodies from synthetic libraries using CDR-swapping mutagenesis
title_sort facile isolation of high-affinity nanobodies from synthetic libraries using cdr-swapping mutagenesis
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8783142/
https://www.ncbi.nlm.nih.gov/pubmed/35098159
http://dx.doi.org/10.1016/j.xpro.2021.101101
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