Here, we present an MD MS strategy relying on the use of PTCR to investigate an ADC with variable drug-to-antibody ratio, targeting the unambiguous localization of payload conjugation sites. Unlike traditional tandem MS experiments (MS2), which were largely ineffective, a single PTCR-based experiment (MS3) proved to be sufficient to achieve this goal across all modified ADC subunits.
[doi:10.25345/C5NZ8120D]
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: middle down mass spectrometry ; antibody drug conjugate ; biotherapeutics ; proton transfer charge reduction ; electron transfer dissociation ; ultraviolet photodissociation ; Orbitrap
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Principal Investigators: (in alphabetical order) |
Luca Fornelli, University of Oklahoma, United States |
| Submitting User: | Fornelli_Lab |
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