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Data of rational process optimization for the production of a full IgG and its Fab fragment from hybridoma cells

This data article focuses on the production of monoclonal antibodies (mAb) and their fragments Fab and F(ab′)(2). Here, we present the data of an optimization protocol to improve the product yield of a hybridoma cell process using a Design of Experiment (DoE) strategy. Furthermore, the data of the e...

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Detalles Bibliográficos
Autores principales: Röhm, Martina, Handl, Alina, König, Maria, Mavoungou, Chrystelle, Handrick, René, Schindowski, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910301/
https://www.ncbi.nlm.nih.gov/pubmed/27366780
http://dx.doi.org/10.1016/j.dib.2016.05.067
Descripción
Sumario:This data article focuses on the production of monoclonal antibodies (mAb) and their fragments Fab and F(ab′)(2). Here, we present the data of an optimization protocol to improve the product yield of a hybridoma cell process using a Design of Experiment (DoE) strategy. Furthermore, the data of the evaluated conditions were used to test feeding strategies in shake flasks. They were verified in controlled 2 L fed-batch bioreactor processes. Supplementing the culture medium with human insulin-like growth factor-I (IGF-I) and Pluronic F-68, as well as a nutrient rich additive for fed-batch, resulted in improved cell growth correlating with a 7 day elongated process time and a 4.5 fold higher product titer. Finally, a rapid Fab generation protocol and the respective data are presented using different papain digestion and a camelid anti-kappa light chain VHH affinity ligand.