单克隆抗体
色谱法
化学
聚糖
凝胶电泳
抗体
糖蛋白
生物
生物化学
免疫学
作者
H. Yamada,Chiemi Matsumura,Keita Yamada,Koichiro Teshima,Takashi Hiroshima,Mitsuhiro Kinoshita,Shigeo Suzuki,Kazuaki Kakehi
出处
期刊:Electrophoresis
[Wiley]
日期:2017-03-06
卷期号:38 (9-10): 1344-1352
被引量:13
标识
DOI:10.1002/elps.201700014
摘要
mAbs are currently mainstream in biopharmaceuticals, and their market has been growing due to their high target specificity. Characterization of heterogeneities in mAbs is performed to secure their quality and safety by physicochemical analyses. However, they require time‐consuming task, which often strain the resources of drug development in pharmaceuticals. Rapid and direct method to determine the heterogeneities should be a powerful tool for pharmaceutical analysis. Considering the advantages of electrophoresis and MS, this study addresses the combination of SDS‐PAGE and intact mass analysis, which provides direct, rapid, and orthogonal determination of heterogeneities in mAb therapeutics. mAb therapeutics that migrated in SDS‐PAGE were recovered from gel by treatment with SDC‐containing buffer. Usage of SDC‐containing buffer as extraction solvent and ethanol‐based staining solution enhanced the recovery of intact IgG from SDS‐PAGE gels. Recovery of mAbs reached more than 86% with 0.2% SD. The heterogeneities, especially N ‐glycan variants in the recovered mAb therapeutics, were clearly determined by intact mass analysis. We believe that the study is important in pharmaceuticals‧ perspective since orthogonal combination of gel electrophoresis and intact mass analysis should be pivotal role for rapid and precise characterization of mAbs.
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