Proteome alterations in the metal-reducing bacterium Shewanella oneidensis MR-1 in response to
different acute dose challenges (0.3, 0.5, or 1 mM) of the toxic metal chromate [Cr(VI)] were characterized
with multidimensional HPLC−MS/MS. Proteome measurements were performed and compared on both
quadrupole ion traps as well as linear trapping quadrupole mass spectrometers. We have found that
the implementation of multidimensional liquid chromatography on-line with the rapid scanning, high
throughput linear trapping quadrupole platform resulted in a dramatic increase in the number of
measured peptides and, thus, the number of identified proteins. A total of 2406 functionally diverse,
nonredundant proteins were identified in this study, representing a relatively deep proteome coverage
for this organism. The core molecular response to chromate challenge under all three concentrations
consisted predominantly of proteins with annotated functions in transport and binding (e.g., components
of the TonB1 iron transport system, TonB-dependent receptors, and sulfate transporters) as well as a
functionally undefined DNA-binding response regulator (SO2426) that might play a role in mediating
metal stress responses. In addition, proteins annotated as a cytochrome c, a putative azoreductase,
and various proteins involved in general stress protection were up-regulated at the higher Cr(VI) doses
(0.5 and 1 mM) only. Proteins down-regulated in response to metal treatment were distributed across
diverse functional categories, with energy metabolism proteins dominating. The results presented in
this work demonstrate the dynamic dosage response of S. oneidensis to sub-toxic levels of chromate.
Keywords: mass spectrometry • multidimensional liquid chromatography • shotgun proteomics • Shewanella
oneidensis • linear trapping quadrupole • chromate stres