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甘氨酸甜菜碱对高渗重组中国仓鼠卵巢细胞培养物中外源蛋白产生的渗透保护作用在不同细胞系中存在差异。

Osmoprotective effect of glycine betaine on foreign protein production in hyperosmotic recombinant chinese hamster ovary cell cultures differs among cell lines.

作者信息

Ryu J S, Kim T K, Chung J Y, Lee G M

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology 373-1, Kusong-Dong, Yusong-Gu, Taejon 305-701, Korea.

出版信息

Biotechnol Bioeng. 2000 Oct 20;70(2):167-75. doi: 10.1002/1097-0290(20001020)70:2<167::aid-bit6>3.0.co;2-p.

Abstract

When three recombinant Chinese hamster ovary (rCHO) cell lines, CHO/dhfr-B22-4, CS13-1.00*, and CS13-0.02*, were cultivated in hyperosmolar media resulting from NaCl addition, their specific foreign protein productivity increased with medium osmolality. However, due to a simultaneous suppression of cell growth at elevated osmolality, no enhancement in the maximum foreign protein titer was made in batch cultures. To test the feasibility of using glycine betaine, known as a strong osmoprotective compound, for improved foreign protein production in hyperosmotic rCHO cell cultures, hyperosmotic batch cultures were carried out in the presence of 15 mM glycine betaine. Glycine betaine was found to have a strong osmoprotective effect on all three rCHO cell lines. Inclusion of 15 mM glycine betaine in hyperosmolar medium enabled rCHO cell lines to grow at 557 to 573 mOsm/kg, whereas they could not grow in the absence of glycine betaine. However, effect of glycine betaine inclusion in hyperosmolar medium on foreign protein production differed among rCHO cell lines. CHO/dhfr-B22-4 cells retained enhanced specific human thrombopoietin (hTPO) productivity in the presence of glycine betaine, and thereby the maximum hTPO titer obtained at 573 mOsm/kg was increased by 72% over that obtained in the control culture with physiological osmolality (292 mOsm/kg). On the other hand, enhanced specific antibody productivity of CS13-1.00* and CS13-0.02* at elevated osmolality was decreased significantly in the presence of glycine betaine. As a result, the maximum antibody titer at 557 mOsm/kg was similar to that obtained in the control culture with physiological osmolality. The mRNA contents per cell determined by northern blot hybridization correlated with q in all three rCHO cell lines, indicating that transcriptional regulation is responsible in part for q enhancement at hyperosmolality in the absence as well as the presence of glycine betaine. Taken together, efficacy of the simultaneous use of hyperosmotic pressure and glycine betaine as a means to improve foreign protein production was variable among different rCHO cell lines.

摘要

当三种重组中国仓鼠卵巢(rCHO)细胞系,即CHO/dhfr - B22 - 4、CS13 - 1.00和CS13 - 0.02,在因添加氯化钠而形成的高渗培养基中培养时,它们的外源蛋白比生产率随培养基渗透压的升高而增加。然而,由于在渗透压升高时细胞生长同时受到抑制,分批培养中最大外源蛋白滴度并未提高。为了测试使用被称为强渗透保护化合物的甘氨酸甜菜碱来提高高渗rCHO细胞培养中外源蛋白产量的可行性,在含有15 mM甘氨酸甜菜碱的情况下进行了高渗分批培养。发现甘氨酸甜菜碱对所有三种rCHO细胞系都有很强的渗透保护作用。在高渗培养基中加入15 mM甘氨酸甜菜碱能使rCHO细胞系在557至573 mOsm/kg下生长,而在没有甘氨酸甜菜碱时它们无法生长。然而,在高渗培养基中加入甘氨酸甜菜碱对外源蛋白生产的影响在不同rCHO细胞系中有所不同。在有甘氨酸甜菜碱存在的情况下,CHO/dhfr - B22 - 4细胞的人血小板生成素(hTPO)比生产率保持提高,因此在573 mOsm/kg下获得的最大hTPO滴度比在生理渗透压(292 mOsm/kg)的对照培养中获得的滴度提高了72%。另一方面,在有甘氨酸甜菜碱存在的情况下,CS13 - 1.00和CS13 - 0.02在渗透压升高时提高的抗体比生产率显著降低。结果,在557 mOsm/kg下的最大抗体滴度与在生理渗透压的对照培养中获得的滴度相似。通过Northern印迹杂交测定的每个细胞的mRNA含量在所有三种rCHO细胞系中都与q相关,表明转录调控在一定程度上负责在有无甘氨酸甜菜碱的情况下高渗时q的提高。综上所述,同时使用高渗压力和甘氨酸甜菜碱作为提高外源蛋白产量的手段,其效果在不同的rCHO细胞系中是可变的。

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