中国仓鼠卵巢细胞
糖基化
重组DNA
化学
生物化学
聚糖
N-连接糖基化
细胞培养
糖蛋白
细胞生物学
生物
基因
受体
遗传学
作者
Yuzhou Fan,Helene Faustrup Kildegaard,Mikael Rørdam Andersen
出处
期刊:Methods in molecular biology
日期:2017-01-01
卷期号:: 209-226
被引量:4
标识
DOI:10.1007/978-1-4939-6972-2_14
摘要
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.
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