Protein Analytical Chemistry, Genentech, 1 DNA Way, South San Francisco, California 94080, United States.
School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, CMU, Rue Michel-Servet, 1, 1206 Geneva, Switzerland.
Anal Chem. 2020 Mar 17;92(6):4357-4363. doi: 10.1021/acs.analchem.9b05193. Epub 2020 Mar 4.
Glycosylation is a common post-translational modification of therapeutic monoclonal antibodies produced in mammalian cells and is considered an important critical quality attribute (CQA), as it is known to impact efficacy, stability, half-life, and immunogenicity. For these reasons, glycosylation requires characterization and close monitoring during the manufacturing process. Due to the complexity of the glycosylation patterns, sophisticated analytical tools with high resolving power are required for the characterization of the glycoforms. This study describes, for the first time, the development and use of an online three-dimensional high-performance liquid chromatography/mass spectrometry (3D-HPLC/MS) approach for the monitoring of glycosylation patterns at the middle-up level. An immobilized IdeS-enzyme column was used in the first dimension for the digestion of mAbs in 10 min. Then, following an online reversed phase liquid chromatography (RPLC) column reduction, the ≈25 kDa proteolytic fragments were analyzed using hydrophilic interaction chromatography (HILIC) coupled to MS. This novel analytical workflow demonstrated the ability to accurately profile glycosylated variants within a total run time of 95 min. To compare the performance of this analytical strategy with a conventional offline procedure (IdeS digestion x reduction-HILIC/MS), a proof of concept study using two mAbs is described here.
糖基化是哺乳动物细胞生产的治疗性单克隆抗体的一种常见翻译后修饰,被认为是一个重要的关键质量属性(CQA),因为它已知会影响疗效、稳定性、半衰期和免疫原性。出于这些原因,糖基化需要在制造过程中进行表征和密切监测。由于糖基化模式的复杂性,需要具有高分辨率的复杂分析工具来对糖型进行表征。本研究首次描述了一种在线三维高效液相色谱/质谱(3D-HPLC/MS)方法的开发和应用,用于在中高水平监测糖基化模式。在第一个维度中,使用固定化 IdeS 酶柱在 10 分钟内对 mAb 进行消化。然后,在线反相液相色谱(RPLC)柱还原后,使用亲水相互作用色谱(HILIC)与 MS 联用分析约 25 kDa 的蛋白水解片段。这种新的分析工作流程展示了在 95 分钟的总运行时间内准确分析糖基化变体的能力。为了比较这种分析策略与传统的离线程序(IdeS 消化 x 还原-HILIC/MS)的性能,本文描述了使用两种 mAb 的概念验证研究。