Rapid and multi-level characterization of trastuzumab using sheathless capillary electrophoresis-tandem mass spectrometry

被引:65
作者
Gahoual, Rabah [1 ]
Burr, Alicia [1 ]
Busnel, Jean-Marc [2 ]
Kuhn, Lauriane [3 ]
Hammann, Phillipe [3 ]
Beck, Alain [4 ]
Francois, Yannis-Nicolas [1 ]
Leize-Wagner, Emmanuelle [1 ]
机构
[1] Univ Strasbourg, LSMIS, UDS CNRS UMR 7140, Strasbourg, France
[2] Beckman Coulter Inc, Brea, CA USA
[3] Univ Strasbourg, Inst Biol Mol & Cellulaire, Strasbourg, France
[4] Ctr Immunol Pierre Fabre, St Julien En Genevois, France
关键词
monoclonal antibody; sheathless capillary electrophoresis; mass spectrometry; CESI-MS; MS; peptide mapping; N-linked glycosylation; posttranslational modifications; microvariant; microheterogeneity; THERAPEUTIC ANTIBODIES; LIQUID-CHROMATOGRAPHY; MONOCLONAL-ANTIBODIES; RECOMBINANT ANTIBODY; CHARGE HETEROGENEITY; POROUS TIP; ELECTROSPRAY; GLYCOSYLATION; PROTEINS; PEPTIDE;
D O I
10.4161/mabs.23995
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:479 / 490
页数:12
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