| Literature DB >> 26774436 |
Jorge Alexander Pavon1, Xiaojuan Li1, Steven Chico1, Umesh Kishnani1, Soundara Soundararajan1, Jason Cheung1, Huijuan Li1, Daisy Richardson1, Mohammed Shameem1, Xiaoyu Yang2.
Abstract
Analysis of oxidation of monoclonal antibodies (mAbs) in most cases relies on peptide mapping and LC-MS, which is time consuming and labor-intensive. A robust chromatography based method that is able to resolve and quantitate mAb oxidation variants due to oxidized methionine or tryptophan is highly desired. Here we developed a novel mixed mode chromatography method using the unique property of Sepax Zenix SEC-300MK column to analyze mAb oxidation levels. The separation of oxidized species relied upon the mixed mode of size exclusion and hydrophobic interaction between the resin and antibodies. The chromatography was performed in a regular SEC mobile phase, PBS, containing NaCl at a concentration (0-2.4M) specific for individual antibodies. This method was able to resolve and quantitate the oxidized antibodies as prepeaks, of either methionine-oxidized species induced by the common oxidants TBHP, tryptophan-oxidized species triggered by AAPH, or oxidized species by UV photo-irradiation. The prepeaks were further characterized by SEC-MALLS as monomers and confirmed by LC-MS as oxidized antibody variants with a mass increase of 16 or 32Da. This method has been successfully applied to monitor multiple monoclonal antibodies of IgG1, IgG2, and IgG4 subclasses.Entities:
Keywords: Methionine; Mixed mode chromatography; Monoclonal antibody; Oxidation; Tryptophan
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Year: 2016 PMID: 26774436 DOI: 10.1016/j.chroma.2015.12.068
Source DB: PubMed Journal: J Chromatogr A ISSN: 0021-9673 Impact factor: 4.759