A CE-MALDI interface based on the use of prestructured sample supports

被引:73
作者
Johnson, T [1 ]
Bergquist, J
Ekman, R
Nordhoff, E
Schürenberg, M
Klöppel, KD
Müller, M
Lehrach, H
Gobom, J
机构
[1] Univ Gothenburg, SU Molndal, Inst Clin Neurosci, SE-43180 Molndal, Sweden
[2] Univ Uppsala, SE-75121 Uppsala, Sweden
[3] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[4] Bruker Dalton, D-28359 Bremen, Germany
关键词
D O I
10.1021/ac0011888
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed an off-line coupling of capillary electrophoresis (CE) to matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry (MALDI-TOF-MS) based on CE fraction collection onto prestructured MALDI sample supports. Analyte carryover and detection sensitivity were investigated using a standard peptide mixture. Low femtomole amounts were detected, and no noticeable carryover was discovered. The performance of the method was evaluated with a mixture of tryptic digests of proteins from a human fetal brain cDNA expression library. The total number of identified peptides was increased from 47 to 211 when the CE-MALDI interface was used compared to direct MALDI-MS analysis. Sequence coverage with CE-MALDI was in the 25-60% range for the different proteins, corresponding to an increase of 1.3-4.9 times relative to that obtained with MALDI-MS of the crude mixture. Fractionation of sample components also facilitated protein identification by MAG DI postsource decay analysis. Our initial results suggest this CE-MALDI interface can be used for the analysis of complex peptide mixtures isolated from biological tissues.
引用
收藏
页码:1670 / 1675
页数:6
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