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A single donor is sufficient to produce a highly functional in vitro antibody library

Antibody complementarity determining region diversity has been considered to be the most important metric for the production of a functional antibody library. Generally, the greater the antibody library diversity, the greater the probability of selecting a diverse array of high affinity leads. Accor...

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Autores principales: Erasmus, M. Frank, D’Angelo, Sara, Ferrara, Fortunato, Naranjo, Leslie, Teixeira, André A., Buonpane, Rebecca, Stewart, Shaun M., Nastri, Horacio G., Bradbury, Andrew R. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979914/
https://www.ncbi.nlm.nih.gov/pubmed/33742103
http://dx.doi.org/10.1038/s42003-021-01881-0
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author Erasmus, M. Frank
D’Angelo, Sara
Ferrara, Fortunato
Naranjo, Leslie
Teixeira, André A.
Buonpane, Rebecca
Stewart, Shaun M.
Nastri, Horacio G.
Bradbury, Andrew R. M.
author_facet Erasmus, M. Frank
D’Angelo, Sara
Ferrara, Fortunato
Naranjo, Leslie
Teixeira, André A.
Buonpane, Rebecca
Stewart, Shaun M.
Nastri, Horacio G.
Bradbury, Andrew R. M.
author_sort Erasmus, M. Frank
collection PubMed
description Antibody complementarity determining region diversity has been considered to be the most important metric for the production of a functional antibody library. Generally, the greater the antibody library diversity, the greater the probability of selecting a diverse array of high affinity leads. According to this paradigm, the primary means of elevating library diversity has been by increasing the number of donors. In the present study we explored the possibility of creating an in vitro antibody library from a single healthy individual, showing that the number of lymphocytes, rather than the number of donors, is the key criterion in the production of a diverse and functional antibody library. We describe the construction of a high-quality phage display library comprising 5 × 10(9) human antibodies by applying an efficient B cell extraction protocol from a single donor and a targeted V-gene amplification strategy favoring specific antibody families for their improved developability profiles. Each step of the library generation process was followed and validated by next generation sequencing to monitor the library quality and diversity. The functionality of the library was tested using several therapeutically relevant targets for which a vast number of different antibodies with desired biophysical properties were obtained.
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spelling pubmed-79799142021-04-12 A single donor is sufficient to produce a highly functional in vitro antibody library Erasmus, M. Frank D’Angelo, Sara Ferrara, Fortunato Naranjo, Leslie Teixeira, André A. Buonpane, Rebecca Stewart, Shaun M. Nastri, Horacio G. Bradbury, Andrew R. M. Commun Biol Article Antibody complementarity determining region diversity has been considered to be the most important metric for the production of a functional antibody library. Generally, the greater the antibody library diversity, the greater the probability of selecting a diverse array of high affinity leads. According to this paradigm, the primary means of elevating library diversity has been by increasing the number of donors. In the present study we explored the possibility of creating an in vitro antibody library from a single healthy individual, showing that the number of lymphocytes, rather than the number of donors, is the key criterion in the production of a diverse and functional antibody library. We describe the construction of a high-quality phage display library comprising 5 × 10(9) human antibodies by applying an efficient B cell extraction protocol from a single donor and a targeted V-gene amplification strategy favoring specific antibody families for their improved developability profiles. Each step of the library generation process was followed and validated by next generation sequencing to monitor the library quality and diversity. The functionality of the library was tested using several therapeutically relevant targets for which a vast number of different antibodies with desired biophysical properties were obtained. Nature Publishing Group UK 2021-03-19 /pmc/articles/PMC7979914/ /pubmed/33742103 http://dx.doi.org/10.1038/s42003-021-01881-0 Text en © The Author(s) 2021 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/.
spellingShingle Article
Erasmus, M. Frank
D’Angelo, Sara
Ferrara, Fortunato
Naranjo, Leslie
Teixeira, André A.
Buonpane, Rebecca
Stewart, Shaun M.
Nastri, Horacio G.
Bradbury, Andrew R. M.
A single donor is sufficient to produce a highly functional in vitro antibody library
title A single donor is sufficient to produce a highly functional in vitro antibody library
title_full A single donor is sufficient to produce a highly functional in vitro antibody library
title_fullStr A single donor is sufficient to produce a highly functional in vitro antibody library
title_full_unstemmed A single donor is sufficient to produce a highly functional in vitro antibody library
title_short A single donor is sufficient to produce a highly functional in vitro antibody library
title_sort single donor is sufficient to produce a highly functional in vitro antibody library
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979914/
https://www.ncbi.nlm.nih.gov/pubmed/33742103
http://dx.doi.org/10.1038/s42003-021-01881-0
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