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全反式维甲酸联合丁酸钠增强重组 CHO 细胞系中特异性单克隆抗体的生产。

All-trans retinoic acid in combination with sodium butyrate enhances specific monoclonal antibody productivity in recombinant CHO cell line.

机构信息

Biotechnology Group, Faculty of Chemical Engineering, Tarbiat Modares University, Tehran, Iran.

Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Bioprocess Biosyst Eng. 2018 Jul;41(7):961-971. doi: 10.1007/s00449-018-1927-y. Epub 2018 Apr 4.

Abstract

The effects of all-trans retinoic acid (RA) and sodium butyrate (NaBu) on growth, viability and antibody production of two types of transfected Chinese hamster ovary cell lines (CHO-K1 and CHO-S) were investigated using a batch mode cell culture. By adding 0.5 mM NaBu in the CHO-K1 cell culture, the cell specific productivity (Q) and antibody concentration increased by five- and threefold, respectively. The optimal concentration of RA was 100 nM which resulted in twofold increase in antibody production. In a combination model, RA applied at early growth phase of CHO-K1 cells followed by addition of NaBu with lowering culture temperature at the end of stationary phase resulted in two- and threefold increase in Q and final antibody concentration, respectively. The latter strategy was also applied on suspended CHO-S cells with enhanced Q and antibody concentration, but to a lesser extent than the CHO-K1 cells. In conclusion, our results demonstrate that the addition of RA and NaBu along with lowering the culture temperature can increase cell culture period as well as Q and the final concentration of recombinant monoclonal antibody in both CHO-K1 and CHO-S cells without any significant change in binding affinity of the mAb.

摘要

研究了全反式视黄酸(RA)和丁酸钠(NaBu)对两种转染中国仓鼠卵巢细胞系(CHO-K1 和 CHO-S)的生长、活力和抗体产生的影响,采用分批式细胞培养。在 CHO-K1 细胞培养中添加 0.5 mM NaBu,细胞比生产率(Q)和抗体浓度分别增加了五倍和三倍。RA 的最佳浓度为 100 nM,可使抗体产量增加两倍。在组合模型中,RA 在 CHO-K1 细胞的早期生长阶段添加,然后在静止期结束时降低培养温度,可使 Q 和最终抗体浓度分别增加两倍和三倍。后一种策略也应用于悬浮的 CHO-S 细胞,可提高 Q 和抗体浓度,但程度低于 CHO-K1 细胞。总之,我们的结果表明,添加 RA 和 NaBu 并降低培养温度可以延长细胞培养周期,提高 Q 和重组单克隆抗体的最终浓度,而 mAb 的结合亲和力没有任何显著变化。

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