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Integration of cell line and process development to overcome the challenge of a difficult to express protein

机译:细胞系和工艺开发的整合克服了难以表达的蛋白质的挑战

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This case study addresses the difficulty in achieving high level expression and production of a small, very positively charged recombinant protein. The novel challenges with this protein include the protein's adherence to the cell surface and its inhibitory effects on Chinese hamster ovary (CHO) cell growth. To overcome these challenges, we utilized a multi-prong approach. We identified dextran sulfate as a way to simultaneously extract the protein from the cell surface and boost cellular productivity. In addition, host cells were adapted to grow in the presence of this protein to improve growth and production characteristics. To achieve an increase in productivity, new cell lines from three different CHO host lines were created and evaluated in parallel with new process development workflows. Instead of a traditional screen of only four to six cell lines in bioreactors, over 130 cell lines were screened by utilization of 15 mL automated bioreactors (AMBR) in an optimal production process specifically developed for this protein. Using the automation, far less manual intervention is required than in traditional bench-top bioreactors, and much more control is achieved than typical plate or shake flask based screens. By utilizing an integrated cell line and process development incorporating medium optimized for this protein, we were able to increase titer more than 10-fold while obtaining desirable product quality. Finally, Monte Carlo simulations were performed to predict the optimal number of cell lines to screen in future cell line development work with the goal of systematically increasing titer through enhanced cell line screening. (c) 2015 American Institute of Chemical Engineers Biotechnol. Prog., 31:1201-1211, 2015
机译:该案例研究解决了难以实现高水平表达和生产小的带正电荷的重组蛋白的困难。该蛋白的新挑战包括该蛋白对细胞表面的粘附及其对中国仓鼠卵巢(CHO)细胞生长的抑制作用。为了克服这些挑战,我们采用了多管齐下的方法。我们将硫酸葡聚糖鉴定为一种同时从细胞表面提取蛋白质和提高细胞生产力的方法。另外,使宿主细胞适应在该蛋白质存在下生长以改善生长和生产特性。为了提高生产率,创建了来自三个不同CHO宿主系的新细胞系,并与新的工艺开发工作流程并行进行了评估。代替传统的在生物反应器中仅筛选4到6个细胞系的方法,通过在针对该蛋白质专门开发的最佳生产过程中利用15 mL自动化生物反应器(AMBR)筛选了130多个细胞系。使用自动化技术,与传统的台式生物反应器相比,所需的人工干预要少得多,并且与典型的基于平板或摇瓶的筛网相比,可以实现更多的控制。通过利用整合的细胞系和整合了针对该蛋白质优化的培养基的工艺开发,我们能够将滴度提高10倍以上,同时获得所需的产品质量。最后,进行了蒙特卡洛模拟,以预测在将来的细胞系开发工作中筛选的最佳细胞系数量,目的是通过增强的细胞系筛选系统地提高滴度。 (c)2015美国化学工程师学会生物技术学会。 Prog。,31:1201-1211,2015

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