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Journal article · Book chapter

Engineer medium and feed for modulating N-glycosylation of recombinant protein production in CHO cell culture

From

Department of Systems Biology, Technical University of Denmark1

Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark2

Network Engineering of Eukaryotic Cell Factories, Department of Systems Biology, Technical University of Denmark3

CHO Cell Line Engineering and Design, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark4

CHO Core, Translational Management, Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark5

Chinese hamster ovary (CHO) cells have become the primary expression system for the production of complex recombinant proteins due to their long-term success in industrial scale production and generating appropriate protein N-glycans similar to that of humans. Control and optimization of protein N-glycosylation is crucial, as the structure of N-glycans can largely influence both biological and physicochemical properties of recombinant proteins.

Protein N-glycosylation in CHO cell culture can be controlled and tuned by engineering medium, feed, culture process, as well as genetic elements of the cell. In this chapter, we will focus on how to carry out experiments for N-glycosylation modulation through medium and feed optimization. The workflow and typical methods involved in the experiment process will be presented.

Language: English
Publisher: Springer
Year: 2017
Pages: 209-226
Series: Methods in Molecular Biology
ISSN: 19406029 and 10643745
Types: Journal article and Book chapter
DOI: 10.1007/978-1-4939-6972-2_14
ORCIDs: Fan, Yuzhou , Kildegaard, Helene Faustrup and Andersen, Mikael Rørdam

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