From Discovery to Delivery: A Rapid and Targeted Proteomics Workflow for Monitoring Chinese Hamster Ovary Biomanufacturing.

IF 6.1 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Charles Eldrid, Ellie Hawke, Kathleen M Cain, Kate Meeson, Joanne Watson, Reynard Spiess, Luke Johnston, William Smith, Matthew Russell, Robyn Hoare, John Raven, Jean-Marc Schwartz, Magnus Rattray, Leon Pybus, Alan Dickson, Andrew Pitt, Perdita Barran
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引用次数: 0

Abstract

Chinese hamster ovary (CHO) cells are the industrial workhorse for manufacturing biopharmaceuticals, including monoclonal antibodies. CHO cell line development requires a more data-driven approach for the accelerated identification of hyper-productive cell lines. Traditional methods, which rely on time-consuming hierarchical screening, often fail to elucidate the underlying cellular mechanisms driving optimal bioreactor performance. Big data analytics, coupled with advancements in 'omics' technologies, are revolutionizing the study of industrial cell lines. Translating this knowledge into practical methods widely utilized in industrial biomanufacturing remains a significant challenge. This study leverages discovery proteomics to characterize dynamic changes within the CHO cell proteome during a 14-day fed-batch bioreactor cultivation. Utilizing a global untargeted proteomics workflow on both a ZenoTOF 7600 and a Cyclic IMS QToF, we identify 3358 proteins and present a comprehensive data set that describes the molecular changes that occur within a well characterized host chassis. By mapping relative abundances to key cellular processes, eight protein targets were selected as potential biomarkers. The abundance of these proteins through the production run are quantified using a 15-minute targeted triple quadrupole (MRM) assay which provides a molecular level QC for cell viability. This discovery to target workflow has the potential to assist engineering of new chassis and provide simple read outs of successful bioreactor batches.

从发现到交付:监测中国仓鼠卵巢生物制造的快速和靶向蛋白质组学工作流程。
中国仓鼠卵巢细胞(CHO)是生产包括单克隆抗体在内的生物制药的工业主力。CHO细胞系的发展需要更多的数据驱动的方法来加速鉴定高产细胞系。传统的方法依赖于耗时的分层筛选,往往无法阐明驱动最佳生物反应器性能的潜在细胞机制。大数据分析,加上“组学”技术的进步,正在彻底改变工业细胞系的研究。将这些知识转化为广泛应用于工业生物制造的实际方法仍然是一个重大挑战。本研究利用发现蛋白质组学来表征在14天的间歇投料生物反应器培养过程中CHO细胞蛋白质组的动态变化。利用ZenoTOF 7600和Cyclic IMS QToF的全球非靶向蛋白质组学工作流程,我们鉴定了3358种蛋白质,并提供了一个全面的数据集,描述了在一个特征良好的宿主机箱内发生的分子变化。通过绘制关键细胞过程的相对丰度图,选择了8个蛋白靶点作为潜在的生物标志物。通过15分钟靶向三重四极杆(MRM)测定,这些蛋白质的丰度通过生产运行进行量化,该检测提供了分子水平的细胞活力QC。目标工作流程的发现有可能协助新底盘的工程设计,并提供成功生物反应器批次的简单读出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
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