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Reduced Temperature Production of Recombinant Proteins to Increase Productivity in Mammalian Cell Culture

机译:降低重组蛋白的温度产生以提高哺乳动物细胞培养的生产力

摘要

The production of recombinant proteins from an industrial perspective has one of its main goals is to increase the product concentration whether in batch, fed-batch or continuous perfusion bioreactor systems. However, a major problem trying to achieve high product concentration over prolonged cultivation is the loss of cell viability leading to reduced production rate and lower product quality. One possible means to achieve high product concentration and main high cell viability is to perform the bioreactor operations at a reduced temperature than that traditional used for mammalian cell cultivation.A collaborative research project between MIT and the Bioprocessing Technology Institute (BTI) was established where the MIT Ph.D. candidate (S.R. Fox) performed his research in Singapore with the assistances of BTI personnel. The goal of this project was the production of recombinant gamma interferon (γ -IFN) in Chinese Hamster Ovary (CHO) cells by operating the bioreactor at 32°C in contrast to cultivating the CHO cells at the traditional temperature of 37°C. By reducing the cultivation temperature to 32°C, we have found that the specific γ -IFN productivity can be increased to 400% as compared to the higher temperature (37°). This increase was the result of two factors. First the cell death was reduced at the lower temperature and second, the mRNA for the γ -IFN gene was greater (presumably through decreased mRNA degradation).However, at the reduced temperature, the cell’s specific growth was also impaired. Mutation and selection for higher growth rate strain at the reduced temperature was successful but we are concerned with the genetic stability of such mutants. Therefore a new collaborative project has been initiated using molecular genetics to engineer new CHO strains with higher growth rate at the reduced temperatures. The preliminary findings from this new project will be presented as a poster in this Symposium by Mr. Hong Kiat Tan.
机译:从工业角度看,重组蛋白的生产的主要目标之一是提高分批,补料分批或连续灌注生物反应器系统的产物浓度。然而,试图在长时间的培养中达到高产品浓度的主要问题是细胞活力的丧失,导致生产率降低和产品质量降低。实现高产品浓度和主要高细胞生存能力的一种可能方法是在比传统的哺乳动物细胞培养温度更低的温度下进行生物反应器操作。麻省理工学院与生物工艺技术研究所(BTI)建立了一项合作研究项目,麻省理工学院博士候选人(S.R. Fox)在BTI人员的协助下在新加坡进行了研究。该项目的目标是通过在32°C下操作生物反应器,而不是在37°C的传统温度下培养CHO细胞,在中国仓鼠卵巢(CHO)细胞中产生重组伽马干扰素(γ-IFN)。通过将培养温度降低至32°C,我们发现与较高温度(37°)相比,γ-IFN的比生产率可以提高至400%。该增加是两个因素的结果。首先,在较低的温度下细胞死亡减少,其次,γ-IFN基因的mRNA更大(大概是通过降低mRNA降解)。但是,在降低的温度下,细胞的特异性生长也受到损害。在较低的温度下成功地诱变并选择了较高生长速率的菌株,但我们关注此类突变体的遗传稳定性。因此,已经启动了一个新的合作项目,该项目使用分子遗传学来设计在降低的温度下具有较高生长速率的新CHO菌株。 Hong Kiat Tan先生将在本次研讨会上以海报的形式介绍这个新项目的初步发现。

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