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The production and study of toxic proteins requires inducible expression systems with low basal level expression and high inducibility. Here, we describe bioprocess applications of the pCytTS temperature-regulatable Sindbis virus replicon-based expression system. We used green fluorescent protein as a marker protein to optimize the selection of stable transfected clones with increased expression levels. Using the optimized protocol, clones were constructed that produced the growth-inhibiting, anti-viral protein interferon beta (beta-IFN). Selected clones were analyzed for temperature-dependent beta-IFN production in adherent and suspension cultures in serum free medium. Specific expression levels were around 1.0 x 10(5) IU/10(6) cells/day (0.5 microg/10(6) cells/day) in suspension cultures and over 1.5 x 10(6) IU/mL/day (7.5 microg/mL/day) in hollow fiber reactors using adherent cells. Hexahistidine-tagged beta-IFN purified from T-flask cultures was highly glycosylated and showed high specific activity. beta-IFN mRNA amplified by the viral replicase for 10 days did not show an accumulation of mutations. These data suggest the applicability of the pCytTS-inducible expression system for the production of high-quality glycoproteins in different reactors.

Original publication

DOI

10.1002/bit.10311

Type

Journal article

Journal

Biotechnol Bioeng

Publication Date

20/09/2002

Volume

79

Pages

602 - 609

Keywords

Animals, Biomarkers, Cell Culture Techniques, Cell Line, Cloning, Molecular, Cricetinae, Gene Expression Regulation, Viral, Green Fluorescent Proteins, Humans, Interferon-beta, Kidney, Luminescent Proteins, Recombinant Fusion Proteins, Replicon, Sindbis Virus, Temperature, Transfection