1. Label-free detection of differential protein expression by LC/MALDI mass spectrometry
- Author
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Hendrik Neubert, Ernst S. Henle, Klaus Rumpel, Timothy P Bonnert, Ian T James, and Brandon T. Hunt
- Subjects
Arabinose ,Proteomics ,Proteome ,Peptide ,Fructose ,medicine.disease_cause ,Mass spectrometry ,Biochemistry ,Protein expression ,chemistry.chemical_compound ,medicine ,Escherichia coli ,Trypsin ,Chromatography, High Pressure Liquid ,Label free ,chemistry.chemical_classification ,Reproducibility ,Electronic Data Processing ,Principal Component Analysis ,Chromatography ,Chemistry ,Escherichia coli Proteins ,Computational Biology ,Proteins ,Reproducibility of Results ,General Chemistry ,Glucose ,Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ,Software - Abstract
Protein abundance changes during disease or experimental perturbation are increasingly analyzed by label-free LC/MS approaches. Here we demonstrate the use of LC/MALDI MS for label-free detection of protein expression differences using Escherichia coli cultures grown on arabinose, fructose or glucose as a carbon source. The advantages of MALDI, such as detection of only singly charged ions, and MALDI plate archiving to facilitate retrospective MS/MS data collection are illustrated. MALDI spectra from RP chromatography of tryptic digests of the E. coli lysates were aligned and quantitated using the Rosetta Elucidator system. Approximately 5000 peptide signals were detected in all LC/MALDI runs spanning over 3 orders of magnitude of signal intensity. The average coefficients of variation for all signals across the entire intensity range in all technical replicates were found to be more...
- Published
- 2008