Genetic rearrangement during site specific integration event facilitates cell line development of a bispecific molecule
Autor: | Yan Zhang, Aaron M. D’Antona, Jeffrey K. Marshall, Cecilia Cooley, Ryan Jackobek, Weili Duan, Amy Tam, Eric Sousa, Gabrielle Bitzas, Sam Zhang, John J. Scarcelli, Lam Khetemenee, Barbara Tevelev, Himakshi Patel, Kathleen Shields, Amy King, Justin Cohen, Wei Wei, Martha Jackson, Lila Wroblewska, Annette Sievers |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
clone (Java method)
medicine.drug_class Transgene multi‐specific molecule Computational biology Biology Monoclonal antibody Transfection RESEARCH ARTICLES Cricetulus bioprocess development Cricetinae Gene duplication medicine Animals Transgenes Gene Retrospective Studies Chinese hamster ovary cell CHO cells Phenotype Recombinant Proteins Cell Culture and Tissue Engineering site‐specific integration gene expression system Biotechnology Research Article |
Zdroj: | Biotechnology Progress |
ISSN: | 1520-6033 8756-7938 |
Popis: | Site Specific Integration (SSI) expression systems offer robust means of generating highly productive and stable cell lines for traditional monoclonal antibodies. As complex modalities such as antibody-like molecules comprised of greater than two peptides become more prevalent, greater emphasis needs to be placed on the ability to produce appreciable quantities of the correct product of interest (POI). The ability to screen several transcript stoichiometries could play a large role in ensuring high amounts of the correct POI. Here we illustrate implementation of an SSI expression system with a single site of integration for development and production of a multi-chain, bi-specific molecule. A SSI vector with a single copy of all of the genes of interest (GOIs) was initially selected for stable Chinese hamster ovary (CHO) transfection. While the resulting transfection pools generated low levels of the desired heterodimer, utilizing an intensive clone screen strategy, we were able to identify clones having significantly higher levels of POI. An in-depth genotypic characterization of clones having the desirable phenotype revealed that a duplication of the light chain within the landing pad was responsible for producing the intended molecule. Retrospective transfection pool analysis using a vector configuration mimicking the transgene configuration found in the clones, as well as other vector configurations, yielded more favorable results with respect to % POI. Overall, the study demonstrated that despite the theoretical static nature of the SSI expression system, enough heterogeneity existed to yield clones having significantly different transgene phenotypes/genotypes and support production of a complex multi-chain molecule. This article is protected by copyright. All rights reserved. |
Databáze: | OpenAIRE |
Externí odkaz: |