Proteomic Analysis of the Sarcosine-Insoluble Outer Membrane Fraction ofHelicobacter pyloriStrain 26695
- 15 February 2004
- journal article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 186 (4) , 949-955
- https://doi.org/10.1128/jb.186.4.949-955.2004
Abstract
Helicobacter pylori causes gastroduodenal disease, which is mediated in part by its outer membrane proteins (OMPs). To identify OMPs of H. pylori strain 26695, we performed a proteomic analysis. A sarcosine-insoluble outer membrane fraction was resolved by two-dimensional electrophoresis with immobilized pH gradient strips. Most of the protein spots, with molecular masses of 10 to 100 kDa, were visible on the gel in the alkaline pI regions (6.0 to 10.0). The proteome of the OMPs was analyzed by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry. Of the 80 protein spots processed, 62 spots were identified; they represented 35 genes, including 16 kinds of OMP. Moreover, we identified 9 immunoreactive proteins by immunoblot analysis. This study contributes to the characterization of the H. pylori strain 26695 proteome and may help to further elucidate the biological function of H. pylori OMPs and the pathogenesis of H. pylori infection.Keywords
This publication has 63 references indexed in Scilit:
- Proteins Released byHelicobacter pyloriIn VitroJournal of Bacteriology, 2002
- Identification of Surface Proteins of Helicobacter pylori by Selective Biotinylation, Affinity Purification, and Two-dimensional Gel ElectrophoresisJournal of Biological Chemistry, 2002
- Pathogenesis of Helicobacter pyloriCurrent Opinion in Gastroenterology, 1998
- Enterochelin acquisition in Campylobacter coli: characterization of components of a binding-protein-dependent transport systemMicrobiology, 1995
- Motility as a factor in the colonisation of gnotobiotic piglets by Helicobacter pyloriJournal of Medical Microbiology, 1992
- Improved silver staining procedure for fast staining in PhastSystem Development Unit. I. Staining of sodium dodecyl sulfate gelsElectrophoresis, 1988
- The Glutamine Synthetase from Azotobacter vinelandii: Purification, Characterization, Regulation and LocalizationEuropean Journal of Biochemistry, 1978
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970