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In-Line Separation by Capillary Electrophoresis Prior to Analysis by Top-Down Mass Spectrometry Enables Sensitive Characterization of Protein Complexes
被引:53
|作者:
Han, Xuemei
[1
]
Wang, Yueju
[1
]
Aslanian, Aaron
[1
,2
]
Fonslow, Bryan
[1
,3
]
Graczyk, Beth
[4
]
Davis, Trisha N.
[4
]
Yates, John R., III
[1
]
机构:
[1] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Mol & Cell Biol Lab, La Jolla, CA 92037 USA
[3] Sciex Separat, Brea, CA 92821 USA
[4] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
关键词:
capillary electrophoresis;
top-down mass spectrometry;
protein complexes;
phosphorylation site mapping;
phosphorylation stoichiometry;
post-translational modification;
POROUS SHEATHLESS INTERFACE;
ZONE-ELECTROPHORESIS;
YEAST PROTEOME;
PHOSPHORYLATION ANALYSIS;
ESCHERICHIA-COLI;
PEPTIDE ANALYSIS;
MITOTIC SPINDLE;
INTACT PROTEINS;
IDENTIFICATION;
SPECTRA;
D O I:
10.1021/pr500971h
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Intact protein analysis via top-down mass spectrometry (MS) provides a birds eye view over the protein complexes and complex protein mixtures with the unique capability of characterizing protein variants, splice isoforms, and combinatorial post-translational modifications (PTMs). Here we applied capillary electrophoresis (CE) through a sheathless CE-electrospray ionization interface coupled to an LTQ Velos Orbitrap Elite mass spectrometer to analyze the Dam1 complex from Saccharomyces cerevisiae. We achieved a 100-fold increase in sensitivity compared to a reversed-phase liquid chromatography coupled MS analysis of recombinant Dam1 complex with a total loading of 2.5 ng (12 amol). N-terminal processing forms of individual subunits of the Dam1 complex were observed as well as their phosphorylation stoichiometry upon Mps1p kinase treatment.
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页码:6078 / 6086
页数:9
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