重组DNA
中国仓鼠卵巢细胞
代谢物
化学
抗体
仿形(计算机编程)
生物化学
生物
免疫学
受体
计算机科学
基因
操作系统
作者
Christopher A. Sellick,Alexandra S. Croxford,Arfa Maqsood,Gill Stephens,Hans V. Westerhoff,Royston Goodacre,Alan J. Dickson
摘要
Abstract Chinese hamster ovary (CHO) cells are the primary platform for commercial expression of recombinant therapeutic proteins. Obtaining maximum production from the expression platform requires optimal cell culture medium (and associated nutrient feeds). We have used metabolite profiling to define the balance of intracellular and extracellular metabolites during the production process of a CHO cell line expressing a recombinant IgG4 antibody. Using this metabolite profiling approach, it was possible to identify nutrient limitations, which acted as bottlenecks for antibody production, and subsequently develop a simple feeding regime to relieve these metabolic bottlenecks. This metabolite profiling‐based strategy was used to design a targeted, low cost nutrient feed that increased cell biomass by 35% and doubled the antibody titer. This approach, with the potential for utilization in non‐specialized laboratories, can be applied universally to the optimization of production of commercially important biopharmaceuticals. Biotechnol. Bioeng. 2011;108: 3025–3031. © 2011 Wiley Periodicals, Inc.
科研通智能强力驱动
Strongly Powered by AbleSci AI