基于CHO稳定池的软传感器开发递归神经网络,用于生产SARS-CoV-2刺突蛋白作为疫苗抗原。

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Sebastian-Juan Reyes, Robert Voyer, Yves Durocher, Olivier Henry, Phuong Lan Pham
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引用次数: 0

摘要

利用中国仓鼠卵巢(CHO)细胞分批饲喂生产重组治疗性蛋白(RTP)的过程可能需要很长一段时间(10 ~ 10天)。在此期间,并非所有的关键特征都可以常规地进行测量,事实上,有些特征只有在过程终止时才进行测量,这使决策制定变得复杂。因此,利用常规的当前生物反应器在线数据来帮助第二天的预测是一个有前途的策略,模型预测控制为基础的投料策略。本文详细介绍了一种拟议的软传感器的开发,该软传感器将当前生物反应器的在线数据和离线历史采样数据合并在一起,以生成关于第二天生产过程的预测。该方法能够在17天的过程中跟踪产品滴度、细胞生长、关键代谢物和累积葡萄糖消耗,具有低归一化均方根误差(nRMSE = 0.24)和低归一化平均绝对误差(nMAE = 0.18),以及与地面数据的高线性(平均R2 = 0.97)。研究还表明,相同的模型架构可以有效地软感知产品滴度和代谢谱(葡萄糖、乳酸、氨),而无需将采样日的离线数据作为模型的输入。这表明,所提出的模型可以作为难以确定变量的真正软传感器,例如依赖于过程结束测量(劳动密集型半定量SDS-PAGE凝胶或ELISA测定)获取数据的三聚体SARS-CoV-2刺突蛋白。瞬时特定葡萄糖消耗率也被预测,并与实验测量结果显示出良好的一致性,进一步为在线葡萄糖控制提供了机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A recurrent neural network for soft sensor development using CHO stable pools in fed-batch process for SARS-CoV-2 spike protein production as a vaccine antigen

A recurrent neural network for soft sensor development using CHO stable pools in fed-batch process for SARS-CoV-2 spike protein production as a vaccine antigen

Fed-batch recombinant therapeutic protein (RTP) production processes utilizing Chinese Hamster Ovary (CHO) cells can take a long period of time (>10 days). Within this period, not all critical features may be measured routinely, and in fact, some are only measured once the process is terminated, complicating decision making. As a consequence, utilizing routine current day bioreactor online data to aid in next day predictions is a promising strategy for model predictive control-based feeding strategies. The article details the development of a proposed soft sensor that merges current day bioreactor online data and offline historical sampling data to generate predictions about the next day of the production process. This approach demonstrated the ability to track product titer, cell growth, key metabolites, and cumulative glucose consumption across the 17-day process with low normalized root mean squared error (nRMSE = 0.24) and low normalized mean absolute error (nMAE = 0.18) as well as high linearity with respect to ground data (average R2 = 0.97). It was also demonstrated that the same model architecture could effectively soft sense product titer and metabolic profiles (glucose, lactate, ammonia) without having sampling day's offline data as inputs to the model. This suggests that the proposed model could act as a true soft sensor of hard-to-determine variables such as the trimeric SARS-CoV-2 spike protein that relies on end-of-process measurements to acquire the data (labor-intensive semi-quantitative SDS-PAGE gels or ELISA assay). Instantaneous specific glucose consumption rates were also predicted and showed good agreement with experimental measurements, further offering opportunities for online glucose control.

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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.
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