Literature DB >> 30227251

Application of a curated genome-scale metabolic model of CHO DG44 to an industrial fed-batch process.

Cyrielle Calmels1, Andréa McCann2, Laetitia Malphettes3, Mikael Rørdam Andersen4.   

Abstract

CHO cells have become the favorite expression system for large scale production of complex biopharmaceuticals. However, industrial strategies for upstream process development are based on empirical results, due to a lack of fundamental understanding of intracellular activities. Genome scale models of CHO cells have been reconstructed to provide an economical way of analyzing and interpreting large-omics datasets, since they add cellular context to the data. Here the most recently available CHO-DG44 genome-scale specific model was manually curated and tailored to the metabolic profile of cell lines used for industrial protein production, by modifying 601 reactions. Generic changes were applied to simplify the model and cope with missing constraints related to regulatory effects as well as thermodynamic and osmotic forces. Cell line specific changes were related to the metabolism of high-yielding production cell lines. The model was semi-constrained with 24 metabolites measured on a daily basis in n = 4 independent industrial 2L fed batch cell culture processes for a therapeutic antibody production. This study is the first adaptation of a genome scale model for CHO cells to an industrial process, that successfully predicted cell phenotype. The tailored model predicted accurately both the exometabolomics data (r2 ≥ 0.8 for 96% of the considered metabolites) and growth rate (r2 = 0.91) of the industrial cell line. Flux distributions at different days of the process were analyzed for validation and suggestion of strategies for medium optimization. This study shows how to adapt a genome scale model to an industrial process and sheds light on the metabolic specificities of a high production process. The curated genome scale model is a great tool to gain insights into intracellular fluxes and to identify possible bottlenecks impacting cell performances during production process. The general use of genome scale models for modeling industrial recombinant cell lines is a long-term investment that will highly benefit process development and speed up time to market.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  Chinese Hamster Ovary; Flux distribution; Genome-scale metabolic model; Metabolic engineering; Model curation

Mesh:

Substances:

Year:  2018        PMID: 30227251     DOI: 10.1016/j.ymben.2018.09.009

Source DB:  PubMed          Journal:  Metab Eng        ISSN: 1096-7176            Impact factor:   9.783


  7 in total

1.  Systematically gap-filling the genome-scale metabolic model of CHO cells.

Authors:  Hamideh Fouladiha; Sayed-Amir Marashi; Shangzhong Li; Zerong Li; Helen O Masson; Behrouz Vaziri; Nathan E Lewis
Journal:  Biotechnol Lett       Date:  2020-10-10       Impact factor: 2.461

2.  Using Metabolomics to Identify Cell Line-Independent Indicators of Growth Inhibition for Chinese Hamster Ovary Cell-based Bioprocesses.

Authors:  Nicholas Alden; Ravali Raju; Kyle McElearney; James Lambropoulos; Rashmi Kshirsagar; Alan Gilbert; Kyongbum Lee
Journal:  Metabolites       Date:  2020-05-15

3.  BiGG Models 2020: multi-strain genome-scale models and expansion across the phylogenetic tree.

Authors:  Charles J Norsigian; Neha Pusarla; John Luke McConn; James T Yurkovich; Andreas Dräger; Bernhard O Palsson; Zachary King
Journal:  Nucleic Acids Res       Date:  2020-01-08       Impact factor: 16.971

Review 4.  Computer-Aided Strategies for Determining the Amino Acid Composition of Medium for Chinese Hamster Ovary Cell-Based Biomanufacturing Platforms.

Authors:  Bergthor Traustason; Matthew Cheeks; Duygu Dikicioglu
Journal:  Int J Mol Sci       Date:  2019-11-02       Impact factor: 5.923

5.  Strategies for Enhancing in vitro Degradation of Linuron by Variovorax sp. Strain SRS 16 Under the Guidance of Metabolic Modeling.

Authors:  Kusum Dhakar; Raphy Zarecki; Daniella van Bommel; Nadav Knossow; Shlomit Medina; Basak Öztürk; Radi Aly; Hanan Eizenberg; Zeev Ronen; Shiri Freilich
Journal:  Front Bioeng Biotechnol       Date:  2021-04-15

6.  Reconstruction of a generic genome-scale metabolic network for chicken: Investigating network connectivity and finding potential biomarkers.

Authors:  Ehsan Salehabadi; Ehsan Motamedian; Seyed Abbas Shojaosadati
Journal:  PLoS One       Date:  2022-03-22       Impact factor: 3.240

Review 7.  Advances of Glycometabolism Engineering in Chinese Hamster Ovary Cells.

Authors:  Huan-Yu Zhang; Zhen-Lin Fan; Tian-Yun Wang
Journal:  Front Bioeng Biotechnol       Date:  2021-12-02
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.