| Literature DB >> 11338578 |
T Johnson1, J Bergquist, R Ekman, E Nordhoff, M Schürenberg, K D Klöppel, M Müller, H Lehrach, J Gobom.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2001 PMID: 11338578 DOI: 10.1021/ac0011888
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986