在自动化平台上集成微尺度蛋白质层析和低 pH 病毒灭活单元操作

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology Progress Pub Date : 2024-04-30 DOI:10.1002/btpr.3476
Paras Sharma, Lars Robbel, Michael Schmitt, Duygu Dikicioglu, Daniel G. Bracewell
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引用次数: 0

摘要

高通量工艺开发(HTPD)是为节省时间和资源的色谱工艺开发而建立的。然而,在单克隆抗体(mAb)纯化流程中与非色谱操作的整合还不太成熟。一个重要的领域是开发蛋白 A 层析后的低 pH 病毒灭活 (VI)。然而,微尺度 pH 值测量装置的缺乏阻碍了这一技术的实施,妨碍了与周围单元操作的整合,限制了对整体工艺的了解。本研究基于 HTPD 平台的设计和测试,以整合蛋白质 A 和低 pH VI 操作。在自动液体处理机上执行之前,先使用设计和模拟软件来实现这一目标。通过对回收率和分子量含量的分析评估,这些操作成功地转化到了微尺度上。集成平台随后被用作评估低 pH 值保持期间 pH 值对 HMWC 影响的工具。在 pH 值为 3.2-3.7 的范围内,实验室级和微米级洗脱池显示出相似的 HMWC。通过评估进行假设实验所需的资源,突出了该平台的研究能力。与实验室规模的实验相比,该平台降低了资源需求,提高了劳动效率。例如,实验可在 7 小时内完成,而微观尺度和实验室尺度分别需要 105 小时和 3 小时。这为在纯化序列中进一步整合色谱操作以外的其他操作提供了机会,从而为 mAb 工艺开发建立一个适合平台的评估工具。
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Integrated micro-scale protein a chromatography and Low pH viral inactivation unit operations on an automated platform

High throughput process development (HTPD) is established for time- and resource- efficient chromatographic process development. However, integration with non-chromatographic operations within a monoclonal antibody (mAb) purification train is less developed. An area of importance is the development of low pH viral inactivation (VI) that follows protein A chromatography. However, the lack of pH measurement devices at the micro-scale represents a barrier to implementation, which prevents integration with the surrounding unit operations, limiting overall process knowledge. This study is based upon the design and testing of a HTPD platform for integration of the protein A and low pH VI operations. This was achieved by using a design and simulation software before execution on an automated liquid handler. The operations were successfully translated to the micro-scale, as assessed by analysis of recoveries and molecular weight content. The integrated platform was then used as a tool to assess the effect of pH on HMWC during low pH hold. The laboratory-scale and micro-scale elution pools showed comparable HMWC across the pH range 3.2–3.7. The investigative power of the platform is highlighted by evaluating the resources required to conduct a hypothetical experiment. This results in lower resource demands and increased labor efficiency relative to the laboratory-scale. For example, the experiment can be conducted in 7 h, compared to 105 h, translating to labor hours, 3 h and 28 h for the micro-scale and laboratory-scale, respectively. This presents the opportunity for further integration beyond chromatographic operations within the purification sequence, to establish a fit-to-platform assessment tool for mAb process development.

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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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