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Rapid label‐free quantitative analysis of the E. coli BL21(DE3) inner membrane proteome
Authors:Malvina Papanastasiou  Georgia Orfanoudaki  Nikos Kountourakis  Marina Koukaki  Marios Frantzeskos Sardis  Michalis Aivaliotis  Konstantinos C. Tsolis  Spyridoula Karamanou  Anastassios Economou
Affiliation:1. Institute of Molecular Biology and Biotechnology, Foundation for Research & Technology, Iraklio, Greece;2. Department Pathology & Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA;3. Department of Biology, University of Crete, Iraklio, Greece;4. Laboratory of Molecular Bacteriology, Rega Institute, Department of Microbiology and Immunology, Katholieke Universiteit Leuven, Leuven, Belgium
Abstract:Biological membranes define cells and cellular compartments and are essential in regulating bidirectional flow of chemicals and signals. Characterizing their protein content therefore is required to determine their function, nevertheless, the comprehensive determination of membrane‐embedded sub‐proteomes remains challenging. Here, we experimentally characterized the inner membrane proteome (IMP) of the model organism E. coli BL21(DE3). We took advantage of the recent extensive re‐annotation of the theoretical E. coli IMP regarding the sub‐cellular localization of all its proteins. Using surface proteolysis of IMVs with variable chemical treatments followed by nanoLC‐MS/MS analysis, we experimentally identified ~45% of the expressed IMP in wild type E. coli BL21(DE3) with 242 proteins reported here for the first time. Using modified label‐free approaches we quantified 220 IM proteins. Finally, we compared protein levels between wild type cells and those over‐synthesizing the membrane‐embedded translocation channel SecYEG proteins. We propose that this proteomics pipeline will be generally applicable to the determination of IMP from other bacteria.
Keywords:Inner membrane proteome  Label‐free quantitation  LC‐MS/MS  Microbiology  SecYEG over‐expressed  Surface proteolysis
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