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Construction of High Expression Vector System Producing TherapeuticMonoclonal Antibody Through Incorporation of Matrix AttachmentRegion Element: A Preliminary Report

机译:结合基质附着区元件构建生产治疗性单克隆抗体的高表达载体系统的初步研究

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The emergence of monoclonal antibody specific to human growth factor receptor marked the greatestachievement in human fight against cancer. By utilizing a specific antibody, cancer treatment nowadays is getting morespecific and efficient. Despite its achievement, the main drawback of antibody therapy remains at its production level.Low yield and transient expression of antibody by mammalian host cells are among the problems discovered duringantibody production. Many strategies have been implied to increase yield and stability of protein including improvementof vector expression system with DNA elements integration as well as manipulating the bioreactor environment toincrease cell density and attain more products. Our study is currently focused on constructing a high expression vectorsystem using matrix attachment region (MAR) element in targeted therapeutic monoclonal antibody production. In thisstudy, a nuclear halo formation has been successfully optimized for CHO cells. A minimum time of 8 minutes is requiredfor maximum nuclear halo formation, thus exposing the most significant sites containing MAR element in CHO genome.This preliminary step is crucial due to the fact that the nuclear halo formation and MAR elements isolation are specific fordifferent types of cells. Subsequent works are currently being carried out to isolate the MAR element from CHO cellsbased on the time determined from nuclear halo formation. This work is going to be distinctive from previous studies asthe MAR element will be predicted from the host cells genome. The mechanism of which the integrated functional MARelement can increase the antibody production even at random position is through up-regulation of gene transcription byadopting a DNA loop structure of nucleosomes that open the structure for specific transcription factor binding.
机译:特异性针对人类生长因子受体的单克隆抗体的出现标志着人类对抗癌症的最大成就。通过利用特异性抗体,当今的癌症治疗变得更加特异性和有效。尽管取得了成就,但是抗体疗法的主要缺点仍然在于其生产水平。哺乳动物宿主细胞的抗体产量低和瞬时表达是抗体生产过程中发现的问题之一。已经暗示了许多策略来增加蛋白质的产量和稳定性,包括通过DNA元件整合来改善载体表达系统,以及操纵生物反应器环境以增加细胞密度并获得更多的产物。我们的研究目前专注于在靶向治疗性单克隆抗体生产中使用基质附着区(MAR)元件构建高表达载体系统。在这项研究中,已经成功地优化了CHO细胞的核晕形成。为了最大程度地形成核晕,至少需要8分钟的时间,从而暴露出CHO基因组中包含MAR元素的最重要位点。由于核晕的形成和MAR元素的分离对于不同类型的细胞是特定的,这一初步步骤至关重要。目前正在进行后续工作,以根据核晕形成的时间,从CHO细胞中分离出MAR元素。这项工作将与以前的研究有所不同,因为将从宿主细胞基因组中预测出MAR元素。整合的功能性MARelement即使在随机位置也可以增加抗体产生的机制是通过采用核小体的DNA环结构上调基因转录来实现的,该结构为特定的转录因子结合打开了结构。

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