Kinetic models towards an enhanced understanding of diverse ADC conjugation reactions

• Published in: Frontiers in bioengineering and biotechnology Vol. 12; p. 1403644
• Main Authors: Weggen, Jan Tobias, Bean, Ryan, Hui, Kimberly, Wendeler, Michaela, Hubbuch, Jürgen
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 11.07.2024
• Subjects: antibody-drug conjugate (ADC); conjugation reaction; cysteine-conjugates; interchain disulfide; kinetic model; site-specific conjugation; cysteine-conjugates; site-specific conjugation; payload; kinetic model; antibody-drug conjugate (ADC); conjugation reaction; interchain disulfide
• ISSN: 2296-4185; 2296-4185
• DOI: 10.3389/fbioe.2024.1403644

The conjugation reaction is the central step in the manufacturing process of antibody-drug conjugates (ADCs). This reaction generates a heterogeneous and complex mixture of differently conjugated sub-species depending on the chosen conjugation chemistry. The parametrization of the conjugation reaction through mechanistic kinetic models offers a chance to enhance valuable reaction knowledge and ensure process robustness. This study introduces a versatile modeling framework for the conjugation reaction of cysteine-conjugated ADC modalities-site-specific and interchain disulfide conjugation. Various conjugation kinetics involving different maleimide-functionalized payloads were performed, while controlled gradual payload feeding was employed to decelerate the conjugation, facilitating a more detailed investigation of the reaction mechanism. The kinetic data were analyzed with a reducing reversed phase (RP) chromatography method, that can readily be implemented for the accurate characterization of ADCs with diverse drug-to-antibody ratios, providing the conjugation trajectories of the single chains of the monoclonal antibody (mAb). Possible kinetic models for the conjugation mechanism were then developed and selected based on multiple criteria. When calibrating the established model to kinetics involving different payloads, conjugation rates were determined to be payload-specific. Further conclusions regarding the kinetic comparability across the two modalities could also be derived. One calibrated model was used for an exemplary screening of the initial concentrations offering valuable insights for profound understanding of the conjugation process in ADC development.