细胞培养
生物反应器
微尺度化学
生物技术
生产力
生化工程
比例(比率)
质量(理念)
生物
吞吐量
选择(遗传算法)
重组DNA
计算生物学
工艺工程
计算机科学
遗传学
数学
工程类
人工智能
宏观经济学
数学教育
哲学
经济
物理
认识论
基因
电信
无线
量子力学
植物
作者
Yolande Rouiller,Jean‐Marc Bielser,David Brühlmann,Martin Jordan,Hervé Broly,Matthieu Stettler
摘要
The major challenge in the selection process of recombinant cell lines for the production of biologics is the choice, early in development, of a clonal cell line presenting a high productivity and optimal cell growth. Most importantly, the selected candidate needs to generate a product quality profile which is adequate with respect to safety and efficacy and which is preserved across cell culture scales. We developed a high-throughput screening and selection strategy of recombinant cell lines, based on their productivity in shaking 96-deepwell plates operated in fed-batch mode, which enables the identification of cell lines maintaining their high productivity at larger scales. Twelve recombinant cell lines expressing the same antibody with different productivities were selected out of 470 clonal cell lines in 96-deepwell plate fed-batch culture. They were tested under the same conditions in 50 mL vented shake tubes, microscale and lab-scale bioreactors in order to confirm the maintenance of their performance at larger scales. The use of a feeding protocol and culture conditions which are essentially the same across the different scales was essential to maintain productivity and product quality profiles across scales. Compared to currently used approaches, this strategy has the advantage of speeding up the selection process and increases the number of screened clones for getting high-producing recombinant cell lines at manufacturing scale with the desired performance and quality.
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