COSMIC-dFBA:用于生物过程建模的新型多尺度混合框架

IF 6.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Metabolic engineering Pub Date : 2024-02-20 DOI:10.1016/j.ymben.2024.02.012
Saratram Gopalakrishnan , William Johnson , Miguel A. Valderrama-Gomez , Elcin Icten , Jasmine Tat , Michael Ingram , Coral Fung Shek , Pik K. Chan , Fabrice Schlegel , Pablo Rolandi , Cleo Kontoravdi , Nathan E. Lewis
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引用次数: 0

摘要

新陈代谢决定着生物制造中细胞的性能,因为它能促进细胞的生长和提高生产率。然而,即使在控制良好的培养系统中,新陈代谢也是动态的,其目标和资源会发生变化,从而限制了用于工艺设计和优化的机理模型的预测能力。在这里,我们介绍了生物反应器中的细胞目标和状态调控(COSMIC)-dFBA,这是一种多尺度混合建模范例,能准确预测细胞密度、抗体滴度和生物反应器代谢物浓度曲线。通过机器学习,COSMIC-dFBA 将生物反应器中的瞬时代谢物吸收率和分泌率分解为来自各细胞状态(生长或抗体产生状态)的加权贡献,并将这些贡献与基因组尺度的代谢模型进行整合。COSMIC-dFBA的一个主要优势是,它可以仅使用废培养基中的代谢物浓度进行参数设置,尽管使用其他omics数据对代谢模型进行约束可以进一步提高其能力。与标准的 dFBA 模型相比,我们发现该框架在细胞密度和抗体滴度预测方面分别提高了 90% 和 72%。因此,我们证明了我们的混合建模框架能有效捕捉细胞新陈代谢,并扩大了 dFBA 在生物反应器动态条件建模中的适用性。
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COSMIC-dFBA: A novel multi-scale hybrid framework for bioprocess modeling

Metabolism governs cell performance in biomanufacturing, as it fuels growth and productivity. However, even in well-controlled culture systems, metabolism is dynamic, with shifting objectives and resources, thus limiting the predictive capability of mechanistic models for process design and optimization. Here, we present Cellular Objectives and State Modulation In bioreaCtors (COSMIC)-dFBA, a hybrid multi-scale modeling paradigm that accurately predicts cell density, antibody titer, and bioreactor metabolite concentration profiles. Using machine-learning, COSMIC-dFBA decomposes the instantaneous metabolite uptake and secretion rates in a bioreactor into weighted contributions from each cell state (growth or antibody-producing state) and integrates these with a genome-scale metabolic model. A major strength of COSMIC-dFBA is that it can be parameterized with only metabolite concentrations from spent media, although constraining the metabolic model with other omics data can further improve its capabilities. Using COSMIC-dFBA, we can predict the final cell density and antibody titer to within 10% of the measured data, and compared to a standard dFBA model, we found the framework showed a 90% and 72% improvement in cell density and antibody titer prediction, respectively. Thus, we demonstrate our hybrid modeling framework effectively captures cellular metabolism and expands the applicability of dFBA to model the dynamic conditions in a bioreactor.

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来源期刊
Metabolic engineering
Metabolic engineering 工程技术-生物工程与应用微生物
CiteScore
15.60
自引率
6.00%
发文量
140
审稿时长
44 days
期刊介绍: Metabolic Engineering (MBE) is a journal that focuses on publishing original research papers on the directed modulation of metabolic pathways for metabolite overproduction or the enhancement of cellular properties. It welcomes papers that describe the engineering of native pathways and the synthesis of heterologous pathways to convert microorganisms into microbial cell factories. The journal covers experimental, computational, and modeling approaches for understanding metabolic pathways and manipulating them through genetic, media, or environmental means. Effective exploration of metabolic pathways necessitates the use of molecular biology and biochemistry methods, as well as engineering techniques for modeling and data analysis. MBE serves as a platform for interdisciplinary research in fields such as biochemistry, molecular biology, applied microbiology, cellular physiology, cellular nutrition in health and disease, and biochemical engineering. The journal publishes various types of papers, including original research papers and review papers. It is indexed and abstracted in databases such as Scopus, Embase, EMBiology, Current Contents - Life Sciences and Clinical Medicine, Science Citation Index, PubMed/Medline, CAS and Biotechnology Citation Index.
期刊最新文献
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