| Literature DB >> 26053232 |
John E Schiel1, Sarah M Rogstad2, Michael T Boyne2.
Abstract
Monoclonal antibody therapeutics are a heterogeneous mixture of glycoforms. Multiple methods exist for defining the glycan composition and relative abundance of species present. In the current report, two MS-based methods were compared for their ability to both identify glycans and monitor differences in the glycoprofile. Gross changes in the glycoprofile can be identified either by visual inspection of fluorescence profiles and correlated to glycan identities when coupled with online MS/MS (LC-F-MS/MS) or through extracted ion chromatograms using LC-MS. In the present study, both an LC-F-MS/MS method and an automated LC-MS label free approach were able to identify minor differences in low abundance glycoforms, and data indicate a disparity in glycosylation between the analyzed batches of US and foreign-sourced mAb X. Thus, either method may be useful in characterizing monoclonal antibody therapeutics products and could serve as a potential screening test for understanding process, comparability, similarity, and possibly detecting counterfeit agents. Published 2015. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: Fluorescence spectroscopy; Glycosylation; LC-MS; Mass spectrometry; Monoclonal antibody
Mesh:
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Year: 2015 PMID: 26053232 DOI: 10.1002/jps.24522
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534