The relationship of metabolic burden to productivity levels in CHO cell lines

Biotechnol Appl Biochem. 2018 Mar;65(2):173-180. doi: 10.1002/bab.1574. Epub 2017 Aug 18.

Abstract

The growing demand for recombinant therapeutics has driven biotechnologists to develop new production strategies. One such strategy for increasing the expression of heterologous proteins has focused on enhancing cell-specific productivity through environmental perturbations. In this work, the effects of hypothermia, hyperosmolarity, high shear stress, and sodium butyrate treatment on growth and productivity were studied using three (low, medium, and high producing) CHO cell lines that differed in their specific productivities of monoclonal antibody. In all three cell lines, the inhibitory effect of these parameters on proliferation was demonstrated. Additionally, compared to the control, specific productivity was enhanced under all conditions and exhibited a consistent cell line specific pattern, with maximum increases (50-290%) in the low producer, and minimum increases (7-20%) in the high producer. Thus, the high-producing cell line was less responsive to environmental perturbations than the low-producing cell line. We hypothesize that this difference is most likely due to the bottleneck associated with a higher metabolic burden caused by higher antibody expression. Increased recombinant mRNA levels and pyruvate carboxylase activities due to low temperature and hyperosmotic stress were found to be positively associated with the metabolic burden.

Keywords: GS-CHO cell line; environmental perturbation; metabolic burden; monoclonal antibody; specific productivity.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / genetics
  • Antibodies, Monoclonal / metabolism*
  • Batch Cell Culture Techniques / methods*
  • Biotechnology / methods*
  • CHO Cells / cytology
  • CHO Cells / metabolism*
  • Cell Proliferation
  • Cell Survival
  • Cold Temperature
  • Cricetulus
  • Osmotic Pressure
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • Antibodies, Monoclonal
  • Recombinant Proteins