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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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). |
format | Online Article Text |
id | pubmed-8783142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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