Literature DB >> 19373452

Approaches to optimizing animal cell culture process: substrate metabolism regulation and protein expression improvement.

Yuanxing Zhang1.   

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.

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Year:  2009        PMID: 19373452     DOI: 10.1007/10_2008_19

Source DB:  PubMed          Journal:  Adv Biochem Eng Biotechnol        ISSN: 0724-6145            Impact factor:   2.635


  5 in total

Review 1.  Concise Review: Process Development Considerations for Cell Therapy.

Authors:  Andrew Campbell; Thomas Brieva; Lior Raviv; Jon Rowley; Knut Niss; Harvey Brandwein; Steve Oh; Ohad Karnieli
Journal:  Stem Cells Transl Med       Date:  2015-08-27       Impact factor: 6.940

2.  Transient transfection of CHO cells using linear polyethylenimine is a simple and effective means of producing rainbow trout recombinant IFN-γ protein.

Authors:  Ronggai Li
Journal:  Cytotechnology       Date:  2014-06-05       Impact factor: 2.058

3.  Amino acid consumption in naïve and recombinant CHO cell cultures: producers of a monoclonal antibody.

Authors:  L M Carrillo-Cocom; T Genel-Rey; D Araíz-Hernández; F López-Pacheco; J López-Meza; M R Rocha-Pizaña; A Ramírez-Medrano; M M Alvarez
Journal:  Cytotechnology       Date:  2014-05-06       Impact factor: 2.058

4.  Designed Amino Acid Feed in Improvement of Production and Quality Targets of a Therapeutic Monoclonal Antibody.

Authors:  Fatemeh Torkashvand; Behrouz Vaziri; Shayan Maleknia; Amir Heydari; Manouchehr Vossoughi; Fatemeh Davami; Fereidoun Mahboudi
Journal:  PLoS One       Date:  2015-10-19       Impact factor: 3.240

5.  Metabolic engineering of CHO cells for the development of a robust protein production platform.

Authors:  Sanjeev Kumar Gupta; Santosh K Srivastava; Ankit Sharma; Vaibhav H H Nalage; Darshita Salvi; Hiralal Kushwaha; Nikhil B Chitnis; Pratyoosh Shukla
Journal:  PLoS One       Date:  2017-08-01       Impact factor: 3.240

  5 in total

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