共 45 条
Dynamic pH barrage junction focusing of amino acids, peptides, and digested monoclonal antibodies in capillary electrophoresis-mass spectrometry
被引:14
作者:

Wang, Lingyu
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机构:
Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada

Cheng, Jianhui
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Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada

McNutt, Julie E.
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Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada

Morin, Gregg B.
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机构:
BC Canc Res Ctr, Vancouver, BC, Canada Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada

Chen, David D. Y.
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h-index: 0
机构:
Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
机构:
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
[2] BC Canc Res Ctr, Vancouver, BC, Canada
基金:
加拿大自然科学与工程研究理事会;
关键词:
Capillary electrophoresis-mass spectrometry;
Dynamic pH barrage junction;
mAb;
Peptide mapping;
TRANSIENT ISOTACHOPHORETIC STACKING;
ZONE-ELECTROPHORESIS;
SEQUENCE COVERAGE;
PROTEINS;
SENSITIVITY;
ELECTROCHROMATOGRAPHY;
PRECONCENTRATION;
DRUGS;
OPTIMIZATION;
SEPARATION;
D O I:
10.1002/elps.202000076
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Dynamic pH barrage junction focusing in CE enables effective signal enhancement, quantitative capture efficiencies, and straightforward optimization. The method is a technical variant of dynamic pH junction focusing. CE separation with dynamic pH barrage junction focusing is compatible with both optical and mass spectrometric detection. We developed a CE-MS/MS method using hydrophilic polyethyleneimine-coated capillaries and validated it for the qualitative analysis of amino acids, peptides, and tryptic peptides of digested monoclonal antibodies. The S/N of extracted ion electropherograms of zwitterionic analytes were enhanced by approximately two orders of magnitude with a tradeoff of a shortened separation window. Online focusing improved the MS signal intensity of a diluted antibody digest, enabling more precursor ions to be analyzed with subsequent tandem mass spectrometric identification. It also broadened the concentration range of protein digest samples for which adequate sequence coverage data can be obtained. With only 0.9 ng of digested infliximab sample loaded into the capillary, 76% and 100% sequence coverage was realized for antibody heavy and light chains, respectively, after online focusing. Full coverage was achieved with 9 ng of injected digest.
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收藏
页码:1832 / 1842
页数:11
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