Advanced multivariate data analysis to determine the root cause of trisulfide bond formation in a novel antibody-peptide fusion

Biotechnol Bioeng. 2017 Oct;114(10):2222-2234. doi: 10.1002/bit.26339. Epub 2017 Jun 5.

Abstract

Product quality heterogeneities, such as a trisulfide bond (TSB) formation, can be influenced by multiple interacting process parameters. Identifying their root cause is a major challenge in biopharmaceutical production. To address this issue, this paper describes the novel application of advanced multivariate data analysis (MVDA) techniques to identify the process parameters influencing TSB formation in a novel recombinant antibody-peptide fusion expressed in mammalian cell culture. The screening dataset was generated with a high-throughput (HT) micro-bioreactor system (AmbrTM 15) using a design of experiments (DoE) approach. The complex dataset was firstly analyzed through the development of a multiple linear regression model focusing solely on the DoE inputs and identified the temperature, pH and initial nutrient feed day as important process parameters influencing this quality attribute. To further scrutinize the dataset, a partial least squares model was subsequently built incorporating both on-line and off-line process parameters and enabled accurate predictions of the TSB concentration at harvest. Process parameters identified by the models to promote and suppress TSB formation were implemented on five 7 L bioreactors and the resultant TSB concentrations were comparable to the model predictions. This study demonstrates the ability of MVDA to enable predictions of the key performance drivers influencing TSB formation that are valid also upon scale-up. Biotechnol. Bioeng. 2017;114: 2222-2234. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals, Inc.

Keywords: mammalian cell culture; multiple linear regression modeling; multivariate data analysis; partial least squares modeling; product-related variant; trisulfide bond.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / chemistry*
  • Antibodies, Monoclonal / metabolism
  • Binding Sites
  • CHO Cells
  • Combinatorial Chemistry Techniques
  • Computer Simulation
  • Cricetulus
  • Models, Chemical
  • Models, Statistical
  • Multivariate Analysis*
  • Peptides / chemical synthesis*
  • Peptides / metabolism
  • Protein Binding
  • Protein Interaction Mapping / methods*
  • Recombinant Fusion Proteins / chemistry*
  • Recombinant Fusion Proteins / metabolism
  • Sulfides / chemistry*
  • Sulfides / metabolism
  • Temperature

Substances

  • Antibodies, Monoclonal
  • Peptides
  • Recombinant Fusion Proteins
  • Sulfides