化学
分析物
抗体-药物偶联物
离子迁移光谱法
质谱法
结合
色谱法
药品
串联质谱法
碎片(计算)
药物发现
生物分析
分析化学(期刊)
抗体
单克隆抗体
药理学
生物化学
数学
免疫学
医学
操作系统
生物
数学分析
计算机科学
作者
Richard Y.‐C. Huang,Ekaterina G. Deyanova,David Passmore,Vangipuram S. Rangan,Shrikant Deshpande,Adrienne A. Tymiak,Guodong Chen
标识
DOI:10.1007/s13361-015-1203-1
摘要
Antibody-drug conjugates (ADCs) are emerging modalities in the pharmaceutical industry. Characterization of ADC's drug-to-antibody ratio (DAR) becomes a key assessment because of its importance in ADC efficacy and safety. DAR characterization by conventional intact protein MS analysis, however, is challenging because of high heterogeneity of ADC samples. The analysis often requires protein deglycosylation, disulfide-bond reduction, or partial fragmentation. In this study, we illustrate the practical utility of ion mobility mass spectrometry (IM-MS) in a routine LC/MS workflow for DAR measurements. This strategy allows analyte "cleanup" in the gas phase, providing significant improvement of signal-to-noise ratios of ADC intact mass spectra for accurate DAR measurements. In addition, protein drift time analysis offers a new dimension in monitoring the changes of DAR in lot-to-lot analysis.
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