Gahoual Rabah, Burr Alicia, Busnel Jean-Marc, Kuhn Lauriane, Hammann Phillipe, Beck Alain, François Yannis-Nicolas, Leize-Wagner Emmanuelle
Laboratoire de Spectrométrie de Masse des Interactions et des Systèmes (LSMIS); UDS-CNRS UMR 7140; Université de Strasbourg; Strasbourg, France.
Beckman Coulter Inc.; Brea, CA, USA.
MAbs. 2013 May-Jun;5(3):479-90. doi: 10.4161/mabs.23995. Epub 2013 Apr 5.
Monoclonal antibodies (mAbs) are highly complex proteins that display a wide range of microheterogeneity that requires multiple analytical methods for full structure assessment and quality control. As a consequence, the characterization of mAbs on different levels is particularly product - and time - consuming. This work presents the characterization of trastuzumab sequence using sheathless capillary electrophoresis (referred as CESI) - tandem mass spectrometry (CESI-MS/MS). Using this bottom-up proteomic-like approach, CESI-MS/MS provided 100% sequence coverage for both heavy and light chain via peptide fragment fingerprinting (PFF) identification. The result was accomplished in a single shot, corresponding to the analysis of 100 fmoles of digest. The same analysis also enabled precise characterization of the post-translational hot spots of trastuzumab, used as a representative widely marketed therapeutic mAb, including the structural confirmation of the five major N-glycoforms.
单克隆抗体(mAbs)是高度复杂的蛋白质,具有广泛的微异质性,需要多种分析方法来进行完整的结构评估和质量控制。因此,在不同水平上对单克隆抗体进行表征特别耗费产品和时间。这项工作展示了使用无鞘毛细管电泳(称为CESI)-串联质谱(CESI-MS/MS)对曲妥珠单抗序列进行的表征。通过这种类似自下而上的蛋白质组学方法,CESI-MS/MS通过肽片段指纹图谱(PFF)鉴定为重链和轻链提供了100%的序列覆盖率。该结果在一次进样中完成,相当于分析100飞摩尔的酶解产物。同样的分析还能够对曲妥珠单抗的翻译后热点进行精确表征,曲妥珠单抗是一种广泛销售的代表性治疗性单克隆抗体,包括对五种主要N-糖型的结构确认。