Analysis of foreign protein overproduction in recombinant CHO cells. Effect of growth kinetics and cell cycle traverse

Ann N Y Acad Sci. 1994 May 2:721:194-207. doi: 10.1111/j.1749-6632.1994.tb47392.x.

Abstract

Intracellular foreign protein (beta-galactosidase) expression in recombinant CHO cell lines in continuous culture was analyzed by developing a mathematical model that includes the effects of metabolic burden and cell cycle dependence of intracellular foreign protein expression. This combined growth kinetic and cell cycle model, assuming S- or G1-phase-dependent expression, was stimulated to predict productivity on a single-cell and culture-volume basis in continuous cultures. In the case of S-phase-dependent expression, the intracellular foreign protein level increases monotonically, but in the case of G1-phase-dependent expression it decreases monotonically with increasing dilution rate. Also, the trends of foreign protein concentration in the culture volume differ significantly between S- and G1-dependent expression kinetics. Thus, the cell cycle dependency of foreign protein expression should be included in process optimization concepts and operating strategies of continuous bioreactors.

MeSH terms

  • Animals
  • CHO Cells / cytology
  • CHO Cells / metabolism*
  • Cell Cycle
  • Cell Division
  • Cricetinae
  • DNA, Recombinant / genetics
  • Genetic Engineering
  • Kinetics
  • Models, Biological
  • Recombinant Proteins / biosynthesis*
  • Recombinant Proteins / genetics
  • beta-Galactosidase / biosynthesis
  • beta-Galactosidase / genetics

Substances

  • DNA, Recombinant
  • Recombinant Proteins
  • beta-Galactosidase