Top-down analysis of basic proteins by microchip capillary electrophoresis mass spectrometry

被引:36
作者
Akashi, Satoko
Suzuki, Koichi
Arai, Akihiro
Yamada, Naoyuki
Suzuki, Ei-Ichiro
Hirayama, Kazuo
Nakamura, Shin
Nishimura, Yoshifumi
机构
[1] Yokohama City Univ, Int Grad Sch Arts & Sci, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] Shimadzu Co Ltd, Life Sci Lab, Kyoto 6048511, Japan
[3] Ajinomoto Co Inc, Inst Life Sci, Kawasaki Ku, Kawasaki, Kanagawa 2108681, Japan
关键词
D O I
10.1002/rcm.2541
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A system of microchip capillary electrophoresis/electrospray ionization mass spectrometry (mu chip-CE/ESI-MS) for rapid characterization of proteins has been developed. Capillary electrophoresis (CE) enables rapid analysis of a sample present in very small quantity, such as at femtomole levels, at high resolution. Faster CE/MS analysis is expected by downsizing the normal capillary to the microchip (mu chip) capillary. Although rapidity and high resolution are advantages of CE separation, electro-osmotic flow (EOF) instability caused by the interaction between proteins and the microchannel surface results in low reproducibility in the analysis of basic proteins under neutral pH conditions. By coating the microchannel surface with a basic polymer, polyE-323, basic proteins, which have pI values of over 7.5, could be separated and detected by mu chip-CE/MS on quadrupole (Q) and time-of-flight (TOF) hybrid instruments. By increasing the cone and collision voltages during the analysis by mu chip-CE/ESI-MS of a small protein, some product ions, which contain the sequence information, could also be obtained, i.e., 'top-down' analysis of the protein could be accomplished with this mu chip-CE/MS system. To our knowledge, this is the first report of 'top-down' analysis of a protein by mu chip-CE/MS. Since it requires a much shorter time and a smaller sample amount for analysis than the conventional liquid chromatography (LC)/ESI-MS method, mu chip-CE/MS promises to be suitable for the high-throughput characterization of proteins. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:1932 / 1938
页数:7
相关论文
共 36 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]   Analysis of histones by on-line capillary zone electrophoresis-electrospray ionisation mass spectrometry [J].
Aguilar, C ;
Hofte, AJP ;
Tjaden, UR ;
van der Greef, J .
JOURNAL OF CHROMATOGRAPHY A, 2001, 926 (01) :57-67
[3]  
Bergquist J, 2003, CURR OPIN MOL THER, V5, P310
[4]   Proteomics by FTICR mass spectrometry: Top down and bottom up [J].
Bogdanov, B ;
Smith, RD .
MASS SPECTROMETRY REVIEWS, 2005, 24 (02) :168-200
[5]   The role of electron capture dissociation in biomolecular analysis [J].
Cooper, HJ ;
Håkansson, K ;
Marshall, AG .
MASS SPECTROMETRY REVIEWS, 2005, 24 (02) :201-222
[6]  
Foret F, 2000, ELECTROPHORESIS, V21, P1363, DOI 10.1002/(SICI)1522-2683(20000401)21:7<1363::AID-ELPS1363>3.3.CO
[7]  
2-L
[8]   CAPILLARY ZONE ELECTROPHORESIS SEPARATIONS OF BASIC AND ACIDIC PROTEINS USING POLY(VINYL ALCOHOL) COATINGS IN FUSED-SILICA CAPILLARIES [J].
GILGES, M ;
KLEEMISS, MH ;
SCHOMBURG, G .
ANALYTICAL CHEMISTRY, 1994, 66 (13) :2038-2046
[9]   Place of pattern in proteomic biomarker discovery [J].
Gillette, MA ;
Mani, DR ;
Carr, SA .
JOURNAL OF PROTEOME RESEARCH, 2005, 4 (04) :1143-1154
[10]   Comparison between TRF2 and TRF1 of their telomeric DNA-bound structures and DNA-binding activities [J].
Hanaoka, S ;
Nagadoi, A ;
Nishimura, Y .
PROTEIN SCIENCE, 2005, 14 (01) :119-130