Approaches to optimizing animal cell culture process: substrate metabolism regulation and protein expression improvement
- PMID: 19373452
- DOI: 10.1007/10_2008_19
Approaches to optimizing animal cell culture process: substrate metabolism regulation and protein expression improvement
Abstract
Some high value proteins and vaccines for medical and veterinary applications by animal cell culture have an increasing market in China. In order to meet the demands of large-scale productions of proteins and vaccines, animal cell culture technology has been widely developed. In general, an animal cell culture process can be divided into two stages in a batch culture. In cell growth stage a high specific growth rate is expected to achieve a high cell density. In production stage a high specific production rate is stressed for the expression and secretion of qualified protein or replication of virus. It is always critical to maintain high cell viability in fed-batch and perfusion cultures. More concern has been focused on two points by the researchers in China. First, the cell metabolism of substrates is analyzed and the accumulation of toxic by-products is decreased through regulating cell metabolism in the culture process. Second, some important factors effecting protein expression are understood at the molecular level and the production ability of protein is improved. In pace with the rapid development of large-scale cell culture for the production of vaccines, antibodies and other recombinant proteins in China, the medium design and process optimization based on cell metabolism regulation and protein expression improvement will play an important role. The chapter outlines the main advances in metabolic regulation of cell and expression improvement of protein in animal cell culture in recent years.
Similar articles
-
Conversion of a CHO cell culture process from perfusion to fed-batch technology without altering product quality.J Biotechnol. 2006 May 3;123(1):106-16. doi: 10.1016/j.jbiotec.2005.10.013. Epub 2005 Dec 1. J Biotechnol. 2006. PMID: 16324762
-
Automated dynamic fed-batch process and media optimization for high productivity cell culture process development.Biotechnol Bioeng. 2013 Jan;110(1):191-205. doi: 10.1002/bit.24602. Epub 2012 Sep 1. Biotechnol Bioeng. 2013. PMID: 22767053
-
Cell culture process operations for recombinant protein production.Adv Biochem Eng Biotechnol. 2014;139:35-68. doi: 10.1007/10_2013_252. Adv Biochem Eng Biotechnol. 2014. PMID: 24153406
-
Towards dynamic metabolic flux analysis in CHO cell cultures.Biotechnol J. 2012 Jan;7(1):61-74. doi: 10.1002/biot.201100052. Epub 2011 Nov 21. Biotechnol J. 2012. PMID: 22102428 Review.
-
Bioreactor systems for the production of biopharmaceuticals from animal cells.Biotechnol Appl Biochem. 2006 Jul;45(Pt 1):1-12. doi: 10.1042/BA20050233. Biotechnol Appl Biochem. 2006. PMID: 16764553 Review.
Cited by
-
Transient transfection of CHO cells using linear polyethylenimine is a simple and effective means of producing rainbow trout recombinant IFN-γ protein.Cytotechnology. 2015 Dec;67(6):987-93. doi: 10.1007/s10616-014-9737-9. Epub 2014 Jun 5. Cytotechnology. 2015. PMID: 24897997 Free PMC article.
-
Concise Review: Process Development Considerations for Cell Therapy.Stem Cells Transl Med. 2015 Oct;4(10):1155-63. doi: 10.5966/sctm.2014-0294. Epub 2015 Aug 27. Stem Cells Transl Med. 2015. PMID: 26315572 Free PMC article. Review.
-
Designed Amino Acid Feed in Improvement of Production and Quality Targets of a Therapeutic Monoclonal Antibody.PLoS One. 2015 Oct 19;10(10):e0140597. doi: 10.1371/journal.pone.0140597. eCollection 2015. PLoS One. 2015. PMID: 26480023 Free PMC article.
-
Metabolic engineering of CHO cells for the development of a robust protein production platform.PLoS One. 2017 Aug 1;12(8):e0181455. doi: 10.1371/journal.pone.0181455. eCollection 2017. PLoS One. 2017. PMID: 28763459 Free PMC article.
-
Amino acid consumption in naïve and recombinant CHO cell cultures: producers of a monoclonal antibody.Cytotechnology. 2015 Oct;67(5):809-20. doi: 10.1007/s10616-014-9720-5. Epub 2014 May 6. Cytotechnology. 2015. PMID: 24798809 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical