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Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening

Recently, there has been a co-evolution of mammalian libraries and diverse microfluidic approaches for therapeutic antibody hit discovery. Mammalian libraries enable the preservation of full immune repertoires, produce hit candidates in final format and facilitate broad combinatorial bispecific anti...

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Autores principales: Gaa, Ramona, Mayer, Hannah Melina, Noack, Daniela, Kumari, Kavita, Guenther, Ralf, Tsai, Shang-Pu, Ji, Qingyong, Doerner, Achim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469430/
https://www.ncbi.nlm.nih.gov/pubmed/37646089
http://dx.doi.org/10.1080/19420862.2023.2251190
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author Gaa, Ramona
Mayer, Hannah Melina
Noack, Daniela
Kumari, Kavita
Guenther, Ralf
Tsai, Shang-Pu
Ji, Qingyong
Doerner, Achim
author_facet Gaa, Ramona
Mayer, Hannah Melina
Noack, Daniela
Kumari, Kavita
Guenther, Ralf
Tsai, Shang-Pu
Ji, Qingyong
Doerner, Achim
author_sort Gaa, Ramona
collection PubMed
description Recently, there has been a co-evolution of mammalian libraries and diverse microfluidic approaches for therapeutic antibody hit discovery. Mammalian libraries enable the preservation of full immune repertoires, produce hit candidates in final format and facilitate broad combinatorial bispecific antibody screening, while several available microfluidic methodologies offer opportunities for rapid high-content screens. Here, we report proof-of-concept studies exploring the potential of combining microfluidic technologies with mammalian libraries for antibody discovery. First, antibody secretion, target co-expression and integration of appropriate reporter cell lines enabled the selection of in-trans acting agonistic bispecific antibodies. Second, a functional screen for internalization was established and comparison of autocrine versus co-encapsulation setups highlighted the advantages of an autocrine one cell approach. Third, synchronization of antibody-secreting cells prior to microfluidic screens reduced assay variability. Furthermore, a display to secretion switchable system was developed and applied for pre-enrichment of antibody clones with high manufacturability in conjunction with subsequent screening for functional properties. These case studies demonstrate the system’s feasibility and may serve as basis for further development of integrated workflows combining manufacturability sorting and functional screens for the identification of optimal therapeutic antibody candidates.
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spelling pubmed-104694302023-09-01 Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening Gaa, Ramona Mayer, Hannah Melina Noack, Daniela Kumari, Kavita Guenther, Ralf Tsai, Shang-Pu Ji, Qingyong Doerner, Achim MAbs Report Recently, there has been a co-evolution of mammalian libraries and diverse microfluidic approaches for therapeutic antibody hit discovery. Mammalian libraries enable the preservation of full immune repertoires, produce hit candidates in final format and facilitate broad combinatorial bispecific antibody screening, while several available microfluidic methodologies offer opportunities for rapid high-content screens. Here, we report proof-of-concept studies exploring the potential of combining microfluidic technologies with mammalian libraries for antibody discovery. First, antibody secretion, target co-expression and integration of appropriate reporter cell lines enabled the selection of in-trans acting agonistic bispecific antibodies. Second, a functional screen for internalization was established and comparison of autocrine versus co-encapsulation setups highlighted the advantages of an autocrine one cell approach. Third, synchronization of antibody-secreting cells prior to microfluidic screens reduced assay variability. Furthermore, a display to secretion switchable system was developed and applied for pre-enrichment of antibody clones with high manufacturability in conjunction with subsequent screening for functional properties. These case studies demonstrate the system’s feasibility and may serve as basis for further development of integrated workflows combining manufacturability sorting and functional screens for the identification of optimal therapeutic antibody candidates. Taylor & Francis 2023-08-30 /pmc/articles/PMC10469430/ /pubmed/37646089 http://dx.doi.org/10.1080/19420862.2023.2251190 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Report
Gaa, Ramona
Mayer, Hannah Melina
Noack, Daniela
Kumari, Kavita
Guenther, Ralf
Tsai, Shang-Pu
Ji, Qingyong
Doerner, Achim
Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening
title Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening
title_full Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening
title_fullStr Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening
title_full_unstemmed Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening
title_short Mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening
title_sort mammalian display to secretion switchable libraries for antibody preselection and high throughput functional screening
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469430/
https://www.ncbi.nlm.nih.gov/pubmed/37646089
http://dx.doi.org/10.1080/19420862.2023.2251190
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