Enhancement of Human Thyrotropin Synthesis by Sodium Butyrate Addition to Serum-Free CHO Cell Culture
- 31 August 2013
- journal article
- research article
- Published by Springer Nature in Applied Biochemistry and Biotechnology
- Vol. 171 (7) , 1658-1672
Abstract
The influence of sodium butyrate (NaBu) on the synthesis of recombinant human thyrotropin (r-hTSH) by CHO cells was investigated for the first time. A volumetric productivity of ~10 μg hTSH/mL was repeatedly obtained, with a 3.3-fold increase over a control culture carried out in the absence of NaBu. Since NaBu can induce CHO cell apoptosis and cell growth arrest, the increase in specific productivity was even higher, i.e., ca. 5-fold. Analysis of the N-glycan composition of r-hTSH obtained with the addition of NaBu to the culture medium showed an approximately 12 % increase in the amount of sialic acid, as well as in total carbohydrate, partly due to the increase in the site occupancy from 2.77 to 2.93 glycans per mole of hTSH. The two hormone preparations were characterized by N-glycan structural analysis, which showed that NaBu increased the bi-antennary structures by ca. 13 % while decreasing the tri-antennary structures by approximately the same amount. The in vivo biological activity and pharmacokinetic behavior (clearance) were found to be similar for the two hormone preparations.Keywords
This publication has 32 references indexed in Scilit:
- Growth factor withdrawal in combination with sodium butyrate addition extends culture longevity and enhances antibody production in CHO cellsJournal of Biotechnology, 2011
- Strategies for the enhancement of recombinant protein production from mammalian cells by growth arrestBiotechnology Advances, 2010
- Recombinant human thyroid-stimulating hormone as an alternative for thyroid hormone withdrawal in thyroid cancer managementCurrent Opinion in Oncology, 2010
- Increasing the sialylation of therapeutic glycoproteins: The potential of the sialic acid biosynthetic pathwayJournal of Pharmaceutical Sciences, 2009
- Optimal and consistent protein glycosylation in mammalian cell cultureGlycobiology, 2009
- Strategies for analysing and improving the expression and quality of recombinant proteins made in mammalian cellsBiotechnology and Applied Biochemistry, 2009
- Identification of cell culture conditions to control N‐glycosylation site‐occupancy of recombinant glycoproteins expressed in CHO cellsBiotechnology and Bioengineering, 2009
- Sodium butyrate alters erythropoietin glycosylation via multiple mechanismsBiotechnology and Bioengineering, 2007
- Asparagine-linked oligosaccharide structures determine clearance and organ distribution of pituitary and recombinant thyrotropinEndocrinology, 1995
- Purification and characterization of recombinant human thyrotropin (TSH) isoforms produced by Chinese hamster ovary cells: the role of sialylation and sulfation in TSH bioactivityEndocrinology, 1993