The first two authors contributed equally to this work.
Biomarker discovery by CE-MS enables sequence analysis via MS/MS with platform-independent separation
Article first published online: 27 APR 2006
Copyright © 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Special Issue: Capillary Electrophoresis - Mass Spectrometry
Volume 27, Issue 11, pages 2111–2125, No. 11 June 2006
How to Cite
Zürbig, P., Renfrow, M. B., Schiffer, E., Novak, J., Walden, M., Wittke, S., Just, I., Pelzing, M., Neusüß, C., Theodorescu, D., Root, K. E., Ross, M. M. and Mischak, H. (2006), Biomarker discovery by CE-MS enables sequence analysis via MS/MS with platform-independent separation. ELECTROPHORESIS, 27: 2111–2125. doi: 10.1002/elps.200500827
- Issue published online: 30 MAY 2006
- Article first published online: 27 APR 2006
- Manuscript Received: 4 NOV 2005
- Capillary electrophoresis;
- Mass spectrometry;
- Tandem mass spectrometry
CE-MS is a successful proteomic platform for the definition of biomarkers in different body fluids. Besides the biomarker defining experimental parameters, CE migration time and molecular weight, especially biomarker's sequence identity is an indispensable cornerstone for deeper insights into the pathophysiological pathways of diseases or for made-to-measure therapeutic drug design. Therefore, this report presents a detailed discussion of different peptide sequencing platforms consisting of high performance separation method either coupled on-line or off-line to different MS/MS devices, such as MALDI-TOF-TOF, ESI-IT, ESI-QTOF and Fourier transform ion cyclotron resonance, for sequencing indicative peptides. This comparison demonstrates the unique feature of CE-MS technology to serve as a reliable basis for the assignment of peptide sequence data obtained using different separation MS/MS methods to the biomarker defining parameters, CE migration time and molecular weight. Discovery of potential biomarkers by CE-MS enables sequence analysis via MS/MS with platform-independent sample separation. This is due to the fact that the number of basic and neutral polar amino acids of biomarkers sequences distinctly correlates with their CE-MS migration time/molecular weight coordinates. This uniqueness facilitates the independent entry of different sequencing platforms for peptide sequencing of CE-MS-defined biomarkers from highly complex mixtures.