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Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening

Bispecific antibodies offer a clinically validated platform for drug discovery. In generating functionally active bispecific antibodies, it is necessary to identify a unique parental antibody pair to merge into a single molecule. However, technologies that allow high-throughput production of bispeci...

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Autores principales: Kim, Hok Seon, Dunshee, Diana Ronai, Yee, Angie, Tong, Raymond K, Kim, Ingrid, Farahi, Farzam, Hongo, Jo-Anne, Ernst, James A, Sonoda, Junichiro, Spiess, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914367/
https://www.ncbi.nlm.nih.gov/pubmed/28985411
http://dx.doi.org/10.1093/protein/gzx034
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author Kim, Hok Seon
Dunshee, Diana Ronai
Yee, Angie
Tong, Raymond K
Kim, Ingrid
Farahi, Farzam
Hongo, Jo-Anne
Ernst, James A
Sonoda, Junichiro
Spiess, Christoph
author_facet Kim, Hok Seon
Dunshee, Diana Ronai
Yee, Angie
Tong, Raymond K
Kim, Ingrid
Farahi, Farzam
Hongo, Jo-Anne
Ernst, James A
Sonoda, Junichiro
Spiess, Christoph
author_sort Kim, Hok Seon
collection PubMed
description Bispecific antibodies offer a clinically validated platform for drug discovery. In generating functionally active bispecific antibodies, it is necessary to identify a unique parental antibody pair to merge into a single molecule. However, technologies that allow high-throughput production of bispecific immunoglobulin Gs (BsIgGs) for screening purposes are limited. Here, we describe a novel bispecific antibody format termed tethered-variable C(L)BsIgG (tcBsIgG) that allows robust production of intact BsIgG in a single cell line, concurrently ensuring cognate light chain pairing and preserving key antibody structural and functional properties. This technology is broadly applicable in the generation of BsIgG from a variety of antibody isotypes, including human BsIgG1, BsIgG2 and BsIgG4. The practicality of the tcBsIgG platform is demonstrated by screening BsIgGs generated from FGF21-mimetic anti-Klotho-β agonistic antibodies in a combinatorial manner. This screen identified multiple biepitopic combinations with enhanced agonistic activity relative to the parental monoclonal antibodies, thereby demonstrating that biepitopic antibodies can acquire enhanced functionality compared to monospecific parental antibodies. By design, the tcBsIgG format is amenable to high-throughput production of large panels of bispecific antibodies and thus can facilitate the identification of rare BsIgG combinations to enable the discovery of molecules with improved biological function.
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spelling pubmed-59143672018-05-04 Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening Kim, Hok Seon Dunshee, Diana Ronai Yee, Angie Tong, Raymond K Kim, Ingrid Farahi, Farzam Hongo, Jo-Anne Ernst, James A Sonoda, Junichiro Spiess, Christoph Protein Eng Des Sel Original Article Bispecific antibodies offer a clinically validated platform for drug discovery. In generating functionally active bispecific antibodies, it is necessary to identify a unique parental antibody pair to merge into a single molecule. However, technologies that allow high-throughput production of bispecific immunoglobulin Gs (BsIgGs) for screening purposes are limited. Here, we describe a novel bispecific antibody format termed tethered-variable C(L)BsIgG (tcBsIgG) that allows robust production of intact BsIgG in a single cell line, concurrently ensuring cognate light chain pairing and preserving key antibody structural and functional properties. This technology is broadly applicable in the generation of BsIgG from a variety of antibody isotypes, including human BsIgG1, BsIgG2 and BsIgG4. The practicality of the tcBsIgG platform is demonstrated by screening BsIgGs generated from FGF21-mimetic anti-Klotho-β agonistic antibodies in a combinatorial manner. This screen identified multiple biepitopic combinations with enhanced agonistic activity relative to the parental monoclonal antibodies, thereby demonstrating that biepitopic antibodies can acquire enhanced functionality compared to monospecific parental antibodies. By design, the tcBsIgG format is amenable to high-throughput production of large panels of bispecific antibodies and thus can facilitate the identification of rare BsIgG combinations to enable the discovery of molecules with improved biological function. Oxford University Press 2017-09 2017-07-07 /pmc/articles/PMC5914367/ /pubmed/28985411 http://dx.doi.org/10.1093/protein/gzx034 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Kim, Hok Seon
Dunshee, Diana Ronai
Yee, Angie
Tong, Raymond K
Kim, Ingrid
Farahi, Farzam
Hongo, Jo-Anne
Ernst, James A
Sonoda, Junichiro
Spiess, Christoph
Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening
title Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening
title_full Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening
title_fullStr Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening
title_full_unstemmed Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening
title_short Tethered-variable C(L) bispecific IgG: an antibody platform for rapid bispecific antibody screening
title_sort tethered-variable c(l) bispecific igg: an antibody platform for rapid bispecific antibody screening
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914367/
https://www.ncbi.nlm.nih.gov/pubmed/28985411
http://dx.doi.org/10.1093/protein/gzx034
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