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.
引用
收藏
页码:6078 / 6086
页数:9
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