| Literature DB >> 29537936 |
Dan Boyd1, Arpa Ebrahimi1, Sarah Ronan1, Brian Mickus1, Matthew Schenauer1, Jenny Wang1, Darren Brown1, Alexandre Ambrogelly1.
Abstract
Isolation and characterization of monoclonal antibody (mAb) variants to understand the impact of their structure on function is a typical activity during early-stage candidate selection that contributes to derisking clinical development. In particular, efforts are devoted to characterizing oligomeric variants, owing to their potential immunogenic nature. We report here a mAb variant consisting of a canonical mAb monomer associated in a non-covalent fashion with an antigen-binding fragment (Fab) arm amputated from its Fc domain. The truncated heavy chain is encoded in the cell line genome and is the likely product of a genomic recombination during cell line generation. The addition of the Fab arm results in severe loss of potency, indicating its interaction with the Fab domain of the monomer. The presence of such a variant can easily be mitigated by an adequate purification step.Keywords: SEC-MALS; antibody impurities; cell line; high molecular weight species; mAb; molecular size variant; monoclonal antibody; size exclusion chromatography
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Year: 2018 PMID: 29537936 PMCID: PMC5916558 DOI: 10.1080/19420862.2018.1438795
Source DB: PubMed Journal: MAbs ISSN: 1942-0862 Impact factor: 5.857