Controlling the time evolution of mAb N-linked glycosylation, Part I: Microbioreactor experiments
Autor: | Hervé Broly, Matthieu Stettler, Massimo Morbidelli, Anaïs Roulet, Thomas K. Villiger, Arnaud Périlleux, Miroslav Soos |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
chemistry.chemical_classification Glycan Glycosylation biology medicine.drug_class Nucleotide sugar Monoclonal antibody carbohydrates (lipids) 03 medical and health sciences chemistry.chemical_compound 030104 developmental biology Biochemistry chemistry N-linked glycosylation Cell culture Galactose biology.protein medicine Glycoprotein Biotechnology |
Zdroj: | Biotechnology Progress. 32:1123-1134 |
ISSN: | 8756-7938 |
DOI: | 10.1002/btpr.2305 |
Popis: | N-linked glycosylation is of key importance for the efficacy of many biotherapeutic proteins such as monoclonal antibodies (mAbs). Media components and cell culture conditions have been shown to significantly affect N-linked glycosylation during the production of glycoproteins using mammalian cell fed-batch cultures. These parameters inevitably change in modern industrial processes with concentrated feed additions and cell densities beyond 2 × 107 cells/mL. In order to control the time-dependent changes of protein glycosylation, an automated microbioreactor system was used to investigate the effects of culture pH, ammonia, galactose, and manganese chloride supplementation on nucleotide sugars as well as mAb N-linked glycosylation in a time-dependent way. Two different strategies comprising of a single shift of culture conditions as well as multiple media supplementations along the culture duration were applied to obtain changing and constant glycosylation profiles. The different feeding approaches enabled constant glycosylation patterns throughout the entire culture duration at different levels. By modulating the time evolution of the mAb glycan pattern, not only the endpoint but also the ratios between different glycosylation structures could be modified. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:1123-1134, 2016. |
Databáze: | OpenAIRE |
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