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通过离线毛细管电泳-质谱联用的馏分收集富集进行自上而下和中自上而下的方法:应用于单克隆抗体F电荷变体。

Top-down and middle-down approach by fraction collection enrichment using off-line capillary electrophoresis - mass spectrometry coupling: Application to monoclonal antibody F charge variants.

作者信息

Biacchi Michael, Said Nassur, Beck Alain, Leize-Wagner Emmanuelle, François Yannis-Nicolas

机构信息

Laboratoire de Spectrométrie de Masse des Interactions et des Systèmes (LSMIS), UMR 7140 (Unistra-CNRS), Université de Strasbourg, France; Laboratoire de Biochimie Biologie Moléculaire Nutrition Métabolisme, UF 3544 Dépistage Néonatal, CHRU Nancy, France.

Laboratoire de Spectrométrie de Masse des Interactions et des Systèmes (LSMIS), UMR 7140 (Unistra-CNRS), Université de Strasbourg, France.

出版信息

J Chromatogr A. 2017 May 19;1498:120-127. doi: 10.1016/j.chroma.2017.02.064. Epub 2017 Feb 27.

DOI:10.1016/j.chroma.2017.02.064
PMID:28259456
Abstract

The characterization of complex protein mixtures represents one of the biggest challenge in many research fields such as biological or biopharmaceutical sciences. Out of all categories, monoclonal antibodies (mAbs) and related products drawn the most interest due to their strong therapeutic potency and specificity. Because of their intrinsic complexity due to a large number of micro-heterogeneities, there is a crucial need for analytical methods to provide comprehensive in-depth characterization of these proteins. In this work, we developed a methodology using CE-UV/MALDI-MS to perform top-down or middle-down characterization after fraction collection enrichment applied to intact protein and mAbs samples. The performance of the method was evaluated with the rapid separation of three intact protein mixture. Good robustness of CZE separation and quality of MALDI-MS spectra and MALDI-ISD spectra of each protein confirms the usefulness of sample enrichment to obtain adequate quantity of deposed protein for top-down analysis and the proof of principle of the method. In a second step, the method was applied to the middle-down characterization of Fc/2 cetuximab variants. Identification of around 9% sequence coverage of Fc/2 cetuximab fragments allows to conclude on the feasibility of the strategy for middle-down characterization of Fc/2 cetuximab variants using CE-UV/MALDI-MS. Moreover, MALDI-ISD fragmentation of Fc/2 cetuximab variants confirm separation phenomenon based on the formation of Fc/2 dimers with and without C-terminal truncation.

摘要

复杂蛋白质混合物的表征是生物学或生物制药科学等许多研究领域面临的最大挑战之一。在所有类别中,单克隆抗体(mAb)及其相关产品因其强大的治疗效力和特异性而备受关注。由于大量微观异质性导致其内在复杂性,迫切需要分析方法来对这些蛋白质进行全面深入的表征。在这项工作中,我们开发了一种方法,使用CE-UV/MALDI-MS在对完整蛋白质和单克隆抗体样品进行馏分收集富集后进行自上而下或中而下的表征。通过快速分离三种完整蛋白质混合物对该方法的性能进行了评估。CZE分离的良好稳健性以及每种蛋白质的MALDI-MS光谱和MALDI-ISD光谱的质量证实了样品富集对于获得足够量的沉积蛋白质用于自上而下分析的有用性以及该方法的原理证明。在第二步中,该方法应用于Fc/2西妥昔单抗变体的中而下表征。对Fc/2西妥昔单抗片段约9%的序列覆盖率的鉴定使得能够得出使用CE-UV/MALDI-MS对Fc/2西妥昔单抗变体进行中而下表征策略的可行性结论。此外,Fc/2西妥昔单抗变体的MALDI-ISD碎片化证实了基于具有和不具有C末端截短的Fc/2二聚体形成的分离现象。

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