Prediction of methionine oxidation risk in monoclonal antibodies using a machine learning method

MAbs. 2018 Nov-Dec;10(8):1281-1290. doi: 10.1080/19420862.2018.1518887. Epub 2018 Sep 25.

Abstract

Monoclonal antibodies (mAbs) have become a major class of protein therapeutics that target a spectrum of diseases ranging from cancers to infectious diseases. Similar to any protein molecule, mAbs are susceptible to chemical modifications during the manufacturing process, long-term storage, and in vivo circulation that can impair their potency. One such modification is the oxidation of methionine residues. Chemical modifications that occur in the complementarity-determining regions (CDRs) of mAbs can lead to the abrogation of antigen binding and reduce the drug's potency and efficacy. Thus, it is highly desirable to identify and eliminate any chemically unstable residues in the CDRs during the therapeutic antibody discovery process. To provide increased throughput over experimental methods, we extracted features from the mAbs' sequences, structures, and dynamics, used random forests to identify important features and develop a quantitative and highly predictive in silico methionine oxidation model.

Keywords: Chemical stability; QSPR; algorithm; computer aided drug design; elastic network model; in silico modeling; mass spectrometry; molecular modeling; protein structure; structure property relationship.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / chemistry*
  • Antibodies, Monoclonal / metabolism
  • Antigens / metabolism
  • Antineoplastic Agents, Immunological / administration & dosage
  • Antineoplastic Agents, Immunological / chemistry
  • Antineoplastic Agents, Immunological / metabolism
  • Complementarity Determining Regions / chemistry*
  • Complementarity Determining Regions / metabolism
  • Computer Simulation
  • Humans
  • Kinetics
  • Machine Learning*
  • Methionine / chemistry*
  • Oxidation-Reduction
  • Protein Binding
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antigens
  • Antineoplastic Agents, Immunological
  • Complementarity Determining Regions
  • Methionine

Grants and funding

This work was supported by Genentech, Inc., a member of the Roche Group.