4.6 Article

N-glycosylation structure - function characterization of omalizumab, an anti-asthma biotherapeutic product

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ELSEVIER
DOI: 10.1016/j.jpba.2021.114483

Keywords

mAb; N-glycans; Capillary electrophoresis; Structure; Function

Funding

  1. V4-Korea Joint Research Program, project National Research, Development and Innovation Office (NKFIH) of the Hungarian Government [NN 127062]
  2. National Research, Development and Innovation Fund of Hungary [TKP2020-IKA-07, 2020-4.1.1-TKP2020]
  3. [BIONANO_GINOP-2.3.2-15-2016-00017]

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Omalizumab, a glycoprotein based biotherapeutics, is widely used to improve asthma symptoms and reduce corticosteroid usage. The glycosylation of such drugs plays a crucial role in their effectiveness and clearance time, with comprehensive analysis needed during production and release.
Omalizumab, a glycoprotein based biotherapeutics, is one of the most frequently used targeted antibody biopharmaceutical to reduce asthma exacerbations, improve lung function and reduce oral corticosteroid use. The effector function and clearance time of such glycoprotein drugs is affected by their N-glycosylation, that defines the required administration frequency to improve the quality of life in appropriately selected patients. Therefore, the glycosylation of biologics is an important critical quality attribute (CQA). The profile of asparagine linked carbohydrates is greatly dependent on the manufacturing process. Even a small deviation may have a major effect on the structure and therefore the function of the biotherapeutic product. For this reason, comprehensive N-glycosylation analysis is of high importance during production and release. Capillary electrophoresis (CE) is one of the frequently used tools to characterize protein therapeutics and utilized by the biopharmaceutical industry for protein and glycan level analysis, which are key parts both for drug development and quality control. To reveal important structure - function relationships, characterization of omalizumab is presented using capillary SDS gel electrophoresis with UV detection at the protein level and capillary gel electrophoresis with laser induced fluorescent detection at the N-linked carbohydrate level. This latter technique was also used for oligosaccharide sequencing for glycan structure validation. The results suggested no ADCC function - structure relationship due to the mostly core fucosylated biantennary glycans found. However, the presence of the high mannose structures probably affects the clearance rate of the drug. (c) 2021 The Author(s). Published by Elsevier B.V. CC_BY_NC_ND_4.0

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