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开发综合在线二维液相色谱/质谱法,使用亲水相互作用和反相分离,快速、深度分析治疗性抗体。

Development of Comprehensive Online Two-Dimensional Liquid Chromatography/Mass Spectrometry Using Hydrophilic Interaction and Reversed-Phase Separations for Rapid and Deep Profiling of Therapeutic Antibodies.

机构信息

Department of Chemistry , Gustavus Adolphus College , St. Peter , Minnesota 56082 , United States.

Agilent Technologies , Santa Clara , California 95051 , United States.

出版信息

Anal Chem. 2018 May 1;90(9):5923-5929. doi: 10.1021/acs.analchem.8b00776. Epub 2018 Apr 13.

Abstract

Monoclonal antibodies (mAb) and related molecules are being developed at a remarkable pace as new therapeutics for the treatment of diseases ranging from cancer to inflammatory disorders. However, characterization of these molecules at all stages of development and manufacturing presents tremendous challenges to existing analytical technologies because of their large size (ca. 150 kDa) and inherent heterogeneity resulting from complex glycosylation patterns and other post-translational modifications. Multidimensional liquid chromatography is emerging as a powerful platform technology that can be used to both improve analysis speed for these molecules by combining existing one-dimensional separations into a single method (e.g., Protein A affinity separation and size-exclusion chromatography) and increasing the resolving power of separations by moving from one dimension of separation to two. In the current study, we have demonstrated the ability to combine hydrophilic interaction (HILIC) and RP separations in an online comprehensive 2D separation coupled with high resolution MS detection (HILIC × RP-HRMS). We find that active solvent modulation (ASM) is critical for coupling these two separation modes, because it mitigates the otherwise serious negative impact of the acetonitrile-rich HILIC mobile phase on the second dimension RP separation. The chromatograms obtained from these HILIC × RP-HRMS separations of mAbs at the subunit level reveal the extent of glycosylation on the Fc/2 and Fd subunits in analysis times on the order of 2 h. In comparison to previous CEX × RP separations of the same molecules, we find that chromatograms from the HILIC × RP separations are richer and reveal separation of some glycoforms that coelute in the CEX × RP separations.

摘要

单克隆抗体 (mAb) 和相关分子作为治疗从癌症到炎症性疾病等各种疾病的新疗法正在以惊人的速度发展。然而,由于其较大的尺寸(约 150 kDa)以及复杂的糖基化模式和其他翻译后修饰导致的固有异质性,在开发和制造的所有阶段对这些分子进行特征描述都对现有分析技术提出了巨大挑战。多维液相色谱作为一种强大的平台技术正在兴起,可用于通过将现有的一维分离组合成一种方法(例如,蛋白 A 亲和分离和尺寸排阻色谱)来提高这些分子的分析速度(例如,蛋白 A 亲和分离和尺寸排阻色谱),并通过从一维分离到二维分离来提高分离分辨率。在当前的研究中,我们已经证明了在与高分辨率 MS 检测(亲水相互作用 (HILIC) × RP-HRMS)相结合的在线综合二维分离中结合亲水相互作用 (HILIC) 和 RP 分离的能力。我们发现,主动溶剂调制 (ASM) 对于耦合这两种分离模式至关重要,因为它减轻了富含乙腈的 HILIC 流动相对第二维 RP 分离的严重负面影响。在亚基水平上对 mAb 进行的这些 HILIC × RP-HRMS 分离获得的色谱图揭示了 Fc/2 和 Fd 亚基上的糖基化程度,分析时间约为 2 小时。与以前对相同分子的 CEX × RP 分离相比,我们发现 HILIC × RP 分离的色谱图更丰富,并揭示了一些在 CEX × RP 分离中共同洗脱的糖型的分离。

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