| Literature DB >> 29027766 |
Sarantos Kyriakopoulos1, Kok Siong Ang1, Meiyappan Lakshmanan1, Zhuangrong Huang2, Seongkyu Yoon2, Rudiyanto Gunawan3, Dong-Yup Lee1,4.
Abstract
Kinetic modeling is the most suitable framework to describe the dynamic behavior of mammalian cell culture although its industrial application is still in its infancy. Herein, the authors reviewed mammalian bioprocess relevant kinetic models, and found that the simple unstructured-unsegregated approach utilizing empirical Monod-type kinetics based on limiting substrates and inhibitory metabolites is commonly used due to its traceability and simple formalism. Notably, the available kinetic models are typically small to moderate in size, and the development of large-scale models is severely hampered by the scarcity of kinetic data and limitations in current parameter estimation methods. The recent availability of abundant high-throughput multi-omics datasets from mammalian cell cultures have now paved the way to improve parameterization of kinetic models, and integrate regulatory, signaling, and product quality related intracellular events, as well as cellular metabolism within the modeling framework. Ultimately, the authors foresee that multi-scale modeling is the way forward in building predictive kinetic models of mammalian cell culture to advance biomanufacturing.Entities:
Keywords: bioprocessing; kinetic modeling; mammalian cell culture; parameter estimation
Mesh:
Year: 2017 PMID: 29027766 DOI: 10.1002/biot.201700229
Source DB: PubMed Journal: Biotechnol J ISSN: 1860-6768 Impact factor: 4.677