Extensive protein identification efforts from soluble cytoplasmic https://www.selleckchem.com/products/AZD1152-HQPA.html fractions were performed for this study. We estimated the coverage of subcellular proteomes by comparing predicted localizations of experimentally identified proteins with those in silico assigned to the ORFs annotated in the Y. pestis KIM genome. The algorithm used here was PSORTb. Limiting this to the proteins clearly assigned to distinct 2D gel spots, the coverage was roughly 25% for the periplasm, 20% for the cytoplasm, 1% for the IM and 25% for the OM. The prediction of subcellular proteomes is incomplete because assignments are not made for all ORFs (e.g., 45% of the 4086 Y. pestis KIM ORFs using PSORTb). Many proteins were not profiled

quantitatively. However, subcellular fractionation allowed us to increase the number of surveyed proteins and

the dynamic range of abundance measurements. Proteome profiles derived from iron-starved and iron-replete growth conditions, often abbreviated as ‘-Fe and +Fe conditions’ from here on, were compared. learn more When cells were harvested, they were in the stationary phase for at least 3 h (+Fe conditions) or near complete growth arrest due to the lack of iron (-Fe conditions). This is visualized in growth curves at the temperatures of 37°C and 26°C provided in the graphics of Additional File 1. Cells grown in the absence of iron at 37°C consistently reached a 10-20% higher OD600 than those grown at 26°C. Earlier growth time points (exponential phase) would have been of interest, but were not included due to already extensive proteomic Temsirolimus molecular weight profiling efforts. Our rationale was that the greater difference in cell doubling times during the exponential phase (-Fe vs. +Fe) would have confounded identification of iron starvation-specific protein changes more than that for the late growth stage. Differential display experiments were focused on the pH range 4-7 in 2D gels because the majority of mature proteins have pI values ranging from 4 to 7. The removal of basic N-terminal signal sequences from

exported proteins, which are displayed in the periplasmic and mixed membrane fractions, often result in a shift towards more acidic pIs. Few integral IM proteins, typically those with low Mr values, were quantitatively profiled because TMD proteins are too hydrophobic to be sufficiently solubilised or resolved as spots in 2D gels. Periplasmic fractions consistently showed contamination with cytoplasmic proteins which was attributed to partial lysis of Y. pestis spheroplasts during the fractionation. The outcome of this cross-contamination was a moderately decreased depth of analysis for periplasmic proteins. Of nearly 250 statistically significant spot abundance changes with confident protein identifications, observed at 26°C and/or 37°C, some were associated with spot trains. Particularly the 2D profile of the usb-MBR fraction featured extensive spot trains.