Publication | Closed Access
A CE−MALDI Interface Based on the Use of Prestructured Sample Supports
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Citations
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References
2001
Year
EngineeringPrestructured Sample SupportsCe Fraction CollectionProtein PurificationCalibrationBioanalysisAnalytical ChemistryClinical ChemistryInstrumentationElectronic PackagingProteomicsBiophysicsChromatographyCapillary ElectrophoresisBiochemistryComplex Peptide MixturesComputer EngineeringInstrument SciencePeptide LibraryMass SpectrometryProtein Mass SpectrometryElectronic InstrumentationMedicineIdentified PeptidesCe−maldi Interface
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 MALDI 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.
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