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A statistical approach to improve compound screening in cell culture media

机译:一种改善细胞培养基中化合物筛选的统计方法

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摘要

The Chinese hamster ovary (CHO) cell line is widely used for the production of recombinant proteins due to its high growing capacity and productivity, as well as other cell lines derived later than CHO. Adapting cell culture media for each specific cell line is a key to exploit these features for cost effective and fast product generation. Media supplementation is generally addressed by means of one‐factor‐at‐a‐time or classical design of experiments approaches but these techniques may not be efficient enough in preliminary screening phases. In this study, a novel strategy consisting in folding over the Plackett–Burman design was used to increase cell growth and trastuzumab production of different CHO cell lines through supplementation with nonanimal recombinant compounds. Synergies between compounds could be detected with a reduced number of experiments by using this methodology in comparison to more conventional fractional factorial designs. In the particular case reported here, the sequential use of this modified Plackett–Burman in combination with a Box‐Behnken design led to a 1.5‐fold increase in cell growth (10 × 10 cells/mL) and a two‐fold in trastuzumab titer (122 mg/L) in suspension batch culture.
机译:中国仓鼠卵巢(CHO)细胞系由于其高生长能力和高生产力以及其他晚于CHO的细胞系而广泛用于生产重组蛋白。使细胞培养基适应每种特定细胞系是利用这些功能实现经济高效和快速产品生成的关键。通常通过一次一因素或经典设计的实验方法来解决培养基补充问题,但是这些技术在初步筛选阶段可能不够有效。在这项研究中,一种通过折叠Plackett-Burman设计构成的新策略被用于通过补充非动物重组化合物来增加不同CHO细胞系的细胞生长和曲妥珠单抗的产生。与更常规的分数阶乘设计相比,通过使用这种方法,可以通过减少实验次数来检测化合物之间的协同作用。在这里报告的特殊情况下,这种修饰的Plackett-Burman与Box-Behnken设计的顺序使用导致细胞生长增加1.5倍(10×10细胞/ mL),曲妥珠单抗滴度提高两倍(122 mg / L)悬浮液分批培养。

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