| Literature DB >> 29845559 |
Ke Sherry Li1, Phillip Y Chu1, Aimee Fourie-O'Donohue1, Neha Srikumar1, Katherine R Kozak1, Yichin Liu1, John C Tran2.
Abstract
Antibody-drug conjugates (ADCs) present unique challenges for ligand-binding assays primarily due to the dynamic changes of the drug-to-antibody ratio (DAR) distribution in vivo and in vitro. Here, an automated on-tip affinity capture platform with subsequent mass spectrometry analysis was developed to accurately characterize the DAR distribution of ADCs from biological matrices. A variety of elution buffers were tested to offer optimal recovery, with trastuzumab serving as a surrogate to the ADCs. High assay repeatability (CV 3%) was achieved for trastuzumab antibody when captured below the maximal binding capacity of 7.5 μg. Efficient on-tip deglycosylation was also demonstrated in 1 h followed by affinity capture. Moreover, this tip-based platform affords higher throughput for DAR characterization when compared with a well-characterized bead-based method. Graphical Abstract ᅟ.Entities:
Keywords: Affinity capture; Antibody-drug conjugate; Drug antibody ratio
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Year: 2018 PMID: 29845559 DOI: 10.1007/s13361-018-1961-7
Source DB: PubMed Journal: J Am Soc Mass Spectrom ISSN: 1044-0305 Impact factor: 3.109