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Merck
CN
  • The criticality of high-resolution N-linked carbohydrate assays and detailed characterization of antibody effector function in the context of biosimilar development.

The criticality of high-resolution N-linked carbohydrate assays and detailed characterization of antibody effector function in the context of biosimilar development.

mAbs (2015-04-22)
Lowell J Brady, Jyoti Velayudhan, Devi B Visone, Ken C Daugherty, Jeff L Bartron, Michael Coon, Cabot Cornwall, Peter J Hinckley, Lisa Connell-Crowley
摘要

Accurate measurement and functional characterization of antibody Fc domain N-linked glycans is critical to successful biosimilar development. Here, we describe the application of methods to accurately quantify and characterize the N-linked glycans of 2 IgG1 biosimilars with effector function activity, and show the potential pitfalls of using assays with insufficient resolution. Accurate glycan assessment was combined with glycan enrichment using lectin chromatography or production with glycosylation inhibitors to produce enriched pools of key glycan species for subsequent assessment in cell-based antibody-dependent cell-mediated cytotoxicity and complement-dependent cytotoxicity effector function assays. This work highlights the challenges of developing high-quality biosimilar candidates and the need for modern biotechnology capabilities. These results show that high-quality analytics, combined with sensitive cell-based assays to study in vivo mechanisms of action, is an essential part of biosimilar development.

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Sigma-Aldrich
氰基硼氢化钠, reagent grade, 95%
Sigma-Aldrich
氰基硼氢化钠 溶液, 5.0 M in 1 M NaOH
Sigma-Aldrich
3-氨基苯甲酸, 98%
Sigma-Aldrich
氰基硼氢化钠 溶液, 1.0 M in THF