Ion Mobility-Mass Spectrometry and Collision Induced Unfolding Reveal Linker-Payload Effects on Antibody-Drug Conjugate Higher-Order Structure and Stability
) of the ADC was observed. Conjugation at interchain cysteine residues disrupted the HOS of the ADC to a greater extent compared to site-specific conjugates, as evidenced by higher root-mean-square deviation values. CIU data revealed differences in conformation and stability in ADCs with different DARs and different positional isomers with the same DAR. These findings demonstrate the utility of IM-MS and CIU as a high-throughput, information-rich assay for probing the HOS and stability of ADCs during their discovery and development.
Authors
- Eli J. Larson (ORCID: https://orcid.org/0000-0002-1354-0722)
- Hang Hu (ORCID: https://orcid.org/0000-0002-8590-9787)
- Emmanuel Appiah‐Amponsah
- Marion H. Emmert (ORCID: https://orcid.org/0000-0003-4375-8295)
- Devin M. Makey (ORCID: https://orcid.org/0000-0003-2991-6760)
- Rodell C. Barrientos (ORCID: https://orcid.org/0000-0002-6006-5047)
- Brandon T. Ruotolo (ORCID: https://orcid.org/0000-0002-6084-2328)
- Erik L Regalado
Institutions
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- University of Michigan (US)
Publication Details
- Journal
- Bioconjugate Chemistry
- Published
- 2026-04-30
- DOI
- https://doi.org/10.1021/acs.bioconjchem.6c00018
- Primary Topic
- HER2/EGFR in Cancer Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Merck
- National Institute of General Medical Sciences
- National Science Foundation Graduate Research Fellowship Program