Label-free relative quantitative proteomics is a powerful
tool for the survey of protein level changes between two
biological samples. We have developed and applied an
algorithm using chromatographic alignment of μLC−MS
runs to improve the detection of differences between
complex protein mixtures. We demonstrate the performance of our software by finding differences in E. coli
protein abundance upon induction of the lac operon
genes using isopropyl β-d-thiogalactopyranoside. The use
of our alignment gave a 4-fold decrease in mean relative
retention time error and a 6-fold increase in the number
of statistically significant differences between samples.
Using a conservative threshold, we have identified 5290
total μLC−MS regions that have a different abundance
between these samples. Of the detected difference regions, only 23% were mapped to MS/MS peptide identifications. We detected 74 proteins that had a greater
relative abundance in the induced sample and 21 with a
greater abundance in the uninduced sample. We have
developed an effective tool for the label-free detection of
differences between samples and demonstrate an increased sensitivity following chromatographic alignment