Post-Column Denaturation-Assisted Native Size-Exclusion Chromatography–Mass Spectrometry for Rapid and In-Depth Characterization of High Molecular Weight Variants in Therapeutic Monoclonal Antibodies

化学 色谱法 单克隆抗体 质谱法 大小排阻色谱法 表征(材料科学) 洗脱 变性(裂变材料) 串联质谱法 关键质量属性 抗体 生物化学 纳米技术 粒径 材料科学 物理化学 免疫学 生物 核化学
作者
Yuetian Yan,Tao Xing,Anita P. Liu,Zhengqi Zhang,Shunhai Wang,Ning Li
出处
期刊:Journal of the American Society for Mass Spectrometry [American Chemical Society]
卷期号:32 (12): 2885-2894 被引量:7
标识
DOI:10.1021/jasms.1c00289
摘要

The high molecular weight (HMW) size variants present in therapeutic monoclonal antibody (mAb) samples need to be closely monitored and characterized due to their impact on product safety and efficacy. Because of the complexity and often low abundances in final drug substance (DS) samples, characterization of such HMW species is challenging and traditionally requires offline enrichment of the HMW species followed by analysis using various analytical tools. Here, we report the development of a postcolumn denaturation-assisted native SEC-MS method that allows rapid and in-depth characterization of mAb HMW species directly from unfractionated DS samples. This method not only provides high-confidence identification of HMW complexes based on accurate mass measurement of both the intact assembly and the constituent subunits but also allows in-depth analysis of the interaction nature and location. In addition, using the extracted ion chromatograms, derived from high-quality, native-like mass spectra, the elution profiles of each noncovalent and/or nondissociable complex can be readily reconstructed, facilitating the comprehension of a complex HMW profile. The utility of this novel method was demonstrated in different applications, ranging from enriched HMW characterization at late stage development, comparability assessment due to process changes, and forced degradation study of coformulated mAbs. As this method does not require prior enrichment, it is thus desirable for providing both rapid and in-depth characterization of HMW species during the development of therapeutic mAbs.

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