Autophagy-inducing peptide increases CHO cell monoclonal antibody production in batch and fed-batch cultures

Biotechnol Bioeng. 2021 May;118(5):1876-1883. doi: 10.1002/bit.27703. Epub 2021 Feb 19.

Abstract

The development of generic biopharmaceuticals is increasing the pressures for enhanced bioprocess productivity and yields. Autophagy ("self-eating") is a cellular process that allows cells to mitigate stresses such as nutrient deprivation. Reputed autophagy inhibitors have also been shown to increase autophagic flux under certain conditions, and enhance recombinant protein productivity in Chinese Hamster Ovary (CHO) cultures. Since peptides are commonly added to bioprocess culture media in hydrolysates, we evaluated the impact on productivity of an autophagy-inducing peptide (AIP), derived from the cellular autophagy protein Beclin 1. This was analyzed in CHO cell batch and fed-batch serum-free cultures producing a human Immunoglobulin G1 (IgG1). Interestingly, the addition of 1-4 µM AIP enhanced productivity in a concentration-dependent manner. Cell-specific productivity increased up to 1.8-fold in batch cultures, while in fed-batch cultures a maximum twofold increase in IgG concentration was observed. An initial drop in cell viability also occurred before cultures recovered normal growth. Overall, these findings strongly support the value of investigating the effects of autophagy pathway modulation, and in particular, the use of this AIP medium additive to increase CHO cell biotherapeutic protein production and yields.

Keywords: CHO; autophagy; batch; fed-batch; recombinant protein production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / drug effects*
  • Batch Cell Culture Techniques / methods*
  • Bioreactors
  • CHO Cells
  • Cricetinae
  • Cricetulus
  • Culture Media / chemistry
  • Culture Media / metabolism
  • Culture Media / pharmacology
  • Humans
  • Immunoglobulin G / analysis
  • Immunoglobulin G / chemistry
  • Immunoglobulin G / metabolism
  • Peptides / chemistry
  • Peptides / metabolism
  • Peptides / pharmacology
  • Recombinant Proteins* / analysis
  • Recombinant Proteins* / chemistry
  • Recombinant Proteins* / metabolism

Substances

  • Culture Media
  • Immunoglobulin G
  • Peptides
  • Recombinant Proteins