posted on 2016-02-20, 12:37authored byNisha
A. Patel, Andrew Crombie, Susan E. Slade, Konstantinos Thalassinos, Chris Hughes, Joanne B. Connolly, James Langridge, J. Colin Murrell, James H. Scrivens
The proteome of the bacterium Methylocella silvestris has been characterized using reversed phase ultra high pressure
liquid chromatography (UPLC) and two-dimensional reversed phase (high
pH)–reversed phase (low pH) UPLC prior to mass spectrometric
analysis. Variations in protein expression levels were identified
with the aid of label-free quantification in a study of soluble protein
extracts from the organism grown using methane, succinate, or propane
as a substrate. The number of first dimensional fractionation steps
has been varied for 2D analyses, and the impact on data throughput
and quality has been demonstrated. Comparisons have been made regarding
required experimental considerations including total loading of biological
samples required, instrument time, and resulting data file sizes.
The data obtained have been evaluated with respect to number of protein
identifications, confidence of assignments, sequence coverage, relative
levels of proteins, and dynamic range. Good qualitative and quantitative
agreement was observed between the different approaches, and the potential
benefits and limitations of the reversed phase–reversed phase
UPLC technique in label-free analysis are discussed. A preliminary
screen of the protein regulation data has also been performed, providing
evidence for a possible propane assimilation route.