Coupling Capillary Zone Electrophoresis with Electron Transfer Dissociation and Activated Ion Electron Transfer Dissociation for Top-Down Proteomics

被引:45
作者
Zhao, Yimeng [1 ]
Riley, Nicholas M. [2 ,3 ]
Sun, Liangliang [1 ]
Hebert, Alexander S. [2 ,3 ]
Yan, Xiaojing [1 ]
Westphall, Michael S. [2 ,3 ]
Rush, Matthew J. P. [2 ,3 ]
Zhu, Guijie [1 ]
Champion, Matthew M. [1 ]
Medie, Felix Mba [4 ]
Champion, Patricia A. DiGiuseppe [4 ]
Coon, Joshua J. [2 ,3 ]
Dovichi, Norman J. [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[2] Univ Wisconsin, Genome Ctr Wisconsin, Dept Biomol Chem, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[4] Univ Notre Dame, Dept Biol Sci, Notre Dame, IN 46556 USA
基金
美国国家卫生研究院;
关键词
TANDEM MASS-SPECTROMETRY; CAPTURE DISSOCIATION; PROTEIN CHARACTERIZATION; COLLISIONAL ACTIVATION; SEQUENCE-ANALYSIS; HIGH-EFFICIENCY; PEPTIDE; VIRULENCE; TIME; POLYPEPTIDES;
D O I
10.1021/acs.analchem.5b00883
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Top-down proteomics offers the potential for full protein characterization, but many challenges remain for this approach, including efficient protein separations and effective fragmentation of intact proteins. Capillary zone electrophoresis (CZE) has shown great potential for separation of intact proteins, especially for differentially modified proteoforms of the same gene product. To date, however, CZE has been used Only with collision-based fragmentation methods. Here we report the first implementation of electron transfer dissociation (ETD) With online CZE separations for top-down proteomics, analyzing a mixture of four standard proteins and a complex protein mixture from the Mycobacterium marinum bacterial secretome. Using a multipurpose dissociation cell on an Orbitrap Elite system, we demonstrate that CZE is fully compatible with ETD as well as higher energy collisional dissociation (HCD), and that the two complementary fragmentation methods can be used in tandem on the electrophoretic time scale for improved protein characterization. Furthermore, we show that activated ion electron transfer dissociation (AI-ETD), a recently introduced Method for enhanced ETD fragmentation, provides useful performance with CZE separations to greatly increase protein characterization. When combined with HCD, AI-ETD improved the protein sequence coverage by more than 200% for proteins from both standard and complex mixtures, highlighting the benefits electron-driven dissociation methods can add to CZE separations.
引用
收藏
页码:5422 / 5429
页数:8
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