深孔板自动化高通量细胞系开发平台。

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology Progress Pub Date : 2024-02-20 DOI:10.1002/btpr.3442
Xiaoyan Tang, Jorge Quiroz, Yixiao Zhang, Jessica Pan, Zhong Lai, Zhimei Du, Ren Liu
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引用次数: 0

摘要

细胞系开发(CLD)在治疗性生物制剂的生产工艺开发中起着至关重要的作用。大多数生物制剂都是在中国仓鼠卵巢(CHO)细胞中生产的。由于 CHO 基因组中随机转基因整合的特性以及 CHO 固有的可塑性,稳定的 CHO 转染株通常在生产率、生长和产品质量方面存在巨大差异。因此,我们通常必须对大量细胞池和克隆进行筛选,以提高确定理想生产细胞系的概率,而这是一个非常耗费人力和资源的过程。在这里,我们利用 24 孔 DWP(24DWP)、液体处理机和其他自动化组件,开发了一个支持深孔板(DWP)的高通量(DEHT)CLD 平台。该平台的功能涵盖了 CLD 的关键步骤,包括细胞传代、克隆成像和扩增以及喂料批量生产。我们首次证明了 24DWP 适用于 CLD,证实了孔与孔之间和板与板之间的变异性极小,并且不存在孔与孔之间的交叉污染。我们还证明,24DWP 培养物的生长、产量和产品质量与传统摇瓶培养物相当。与传统的 CLD 平台相比,DEHT 平台能让科学家筛选出五倍以上的培养物,从而大大减少了为生物制剂生产确定理想生产细胞系所需的资源。
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A deep-well plate enabled automated high-throughput cell line development platform

Cell line development (CLD) plays a crucial role in the manufacturing process development of therapeutic biologics. Most biologics are produced in Chinese hamster ovary (CHO) cell. Because of the nature of random transgene integration in CHO genome and CHO's inherent plasticity, stable CHO transfectants usually have a vast diversity in productivity, growth, and product quality. Thus, we often must resort to screening a large number of cell pools and clones to increase the probability of identifying the ideal production cell line, which is a very laborious and resource-demanding process. Here we have developed a deep-well plate (DWP) enabled high throughput (DEHT) CLD platform using 24-well DWP (24DWP), liquid handler, and other automation components. This platform has capabilities covering the key steps of CLD including cell passaging, clone imaging and expansion, and fed-batch production. We are the first to demonstrate the suitability of 24DWP for CLD by confirming minimal well-to-well and plate-to-plate variability and the absence of well-to-well cross contamination. We also demonstrated that growth, production, and product quality of 24DWP cultures were comparable to those of conventional shake flask cultures. The DEHT platform enables scientists to screen five times more cultures than the conventional CLD platform, thus significantly decreases the resources needed to identify an ideal production cell line for biologics manufacturing.

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来源期刊
Biotechnology Progress
Biotechnology Progress 工程技术-生物工程与应用微生物
CiteScore
6.50
自引率
3.40%
发文量
83
审稿时长
4 months
期刊介绍: Biotechnology Progress , an official, bimonthly publication of the American Institute of Chemical Engineers and its technological community, the Society for Biological Engineering, features peer-reviewed research articles, reviews, and descriptions of emerging techniques for the development and design of new processes, products, and devices for the biotechnology, biopharmaceutical and bioprocess industries. Widespread interest includes application of biological and engineering principles in fields such as applied cellular physiology and metabolic engineering, biocatalysis and bioreactor design, bioseparations and downstream processing, cell culture and tissue engineering, biosensors and process control, bioinformatics and systems biology, biomaterials and artificial organs, stem cell biology and genetics, and plant biology and food science. Manuscripts concerning the design of related processes, products, or devices are also encouraged. Four types of manuscripts are printed in the Journal: Research Papers, Topical or Review Papers, Letters to the Editor, and R & D Notes.
期刊最新文献
Non-thermal plasma decontamination of microbes: a state of the art. Mechanistic model of minute virus of mice elution behavior in anion exchange chromatography purification. Comparing in silico flowsheet optimization strategies in biopharmaceutical downstream processes. General strategies for IgG-like bispecific antibody purification. Issue Information
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