Literature DB >> 29845559

Automated On-tip Affinity Capture Coupled with Mass Spectrometry to Characterize Intact Antibody-Drug Conjugates from Blood.

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

Mesh:

Substances:

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


  16 in total

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Review 5.  Antibody-drug conjugates: an emerging concept in cancer therapy.

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8.  Antibody-drug conjugates designed to eradicate tumors with homogeneous and heterogeneous expression of the target antigen.

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9.  Pharmacokinetics and biodistribution of the antitumor immunoconjugate, cantuzumab mertansine (huC242-DM1), and its two components in mice.

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  1 in total

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