loading page

SWATH-MS insights on sodium butyrate effect on mAbs production and redox homeostasis in CHO cells
  • +5
  • Mauro Galli,
  • Lillian Chia-Yi Liu,
  • Kae Hwan Sim,
  • Yee Jiun Kok,
  • Katherine Wongtrakul-Kish,
  • Terry Nguyen-Khuong,
  • Stephen Tate,
  • Xuezhi Bi
Mauro Galli
Agency for Science Technology and Research
Author Profile
Lillian Chia-Yi Liu
Agency for Science Technology and Research
Author Profile
Kae Hwan Sim
Agency for Science Technology and Research
Author Profile
Yee Jiun Kok
Agency for Science Technology and Research
Author Profile
Katherine Wongtrakul-Kish
Agency for Science Technology and Research
Author Profile
Terry Nguyen-Khuong
Agency for Science Technology and Research
Author Profile
Stephen Tate
AB Sciex UK Ltd
Author Profile
Xuezhi Bi
Agency for Science Technology and Research

Corresponding Author:[email protected]

Author Profile

Abstract

Sodium butyrate (NaBu), well-known as a histone deacetylase inhibitor and for its capacity to impede cell growth, can enhance the production of a specific protein, such as an antibody, in recombinant Chinese hamster ovary (CHO) cell cultures. In this study, two CHO cell lines, namely K1 and DG44, along with their corresponding mAb-producing lines, K1-Pr and DG44-Pr, were cultivated with or without NaBu. A SWATH-based profiling method was employed to analyze the proteome. Cells cultured in the presence of NaBu exhibited a reduction in mitosis and gene expression, supported by their culture data demonstrating growth inhibition. The presence of NaBu corresponded to an upregulation of intracellular trafficking and secretion pathways, aligned with an observed increase in mAb production. This upregulation was associated with an elevated glycosylation pathway and a slight alteration in the glycosylation profile of the mAbs. The observed increases in fatty acid oxidation, redox interactions, and lipid biosynthesis are likely attributable to the metabolic effects of NaBu. A comprehensive understanding of the systemic effects of NaBu will facilitate the discovery of strategies to enhance or prolong the productivity of CHO cells.