Presentation on theme: "Bacterial Physiology A Proteomic Approach to Oral Diseases Oral Diseases Peter Zilm Microbiology Laboratory Dental School The University of Adelaide."— Presentation transcript:
Bacterial Physiology A Proteomic Approach to Oral Diseases Oral Diseases Peter Zilm Microbiology Laboratory Dental School The University of Adelaide
Genomics versus Proteomics Post Genomic era- Reading of the human genome sequence Relatively few medical breakthroughs derived from genetic research - Can cellular processes be understood by screening genomes? - The organisation and timing of cellular events is not a projection of the genome and its transcription. Proteomics - relies on genomics to facilitate protein identification - which genes are important and under which circumstances - -combination of proteomic and genomic information will likely lead to the understanding of fundamental processes such as cell development and growth, cell differentiation, Cell signaling and cell death.
Proteomic Applications APPROACHESProfilingFunctionalStructural Characterisation of specific sub-sets of the proteome the proteome. Regulons or stimulons Macromolecular complex or sub-cellular compartment Immunogenic proteins Problems with specific post-translational modification Global Characterisation of proteome State1 (Healthy) State 2 (disease) Profile 1 Profile 2 Perturbation (signal)
Step by step Proteomics Sample preparation 2D-P.A.G.E Image analysis Spot identification Data analysis Protein identification Spot cutting & Mass spec. analysis Publishresults
Iso- Electric Focusing In the 1 st dimension, proteins are separated according to their charge. 2-Dimensional Gel Electrophoresis P.A.G.E. In the 2 nd dimension proteins are separated according to their relative In the 2 nd dimension proteins are separated according to their relative mass. mass. Thousands of proteins can be displayed in a single experiment. Thousands of proteins can be displayed in a single experiment. Electrophoretic migration is dependent upon Electrophoretic migration is dependent upon pH charge dependence and “iso-electricity. pH charge dependence and “iso-electricity. Since the 1990’s the position of proteins within Since the 1990’s the position of proteins within gels and their position within the pH gradient gels and their position within the pH gradient could be correlated with the amino acid could be correlated with the amino acid composition of polypeptides. composition of polypeptides.
Iso- Electric Focusing Mol Mass
Protein Staining Techniques Sensitive protein identification methods exist which are compatible withSensitive protein identification methods exist which are compatible with the resolving power of 2D-PAGE. the resolving power of 2D-PAGE.
: P26427P protein has been found in the clicked spot (2D-0015D5): View entry in original SWISS-2DPAGE format Entry name AHPC_ECOLI Primary accession number P26427 Entered in SWISS-2DPAGE in Release 02, August 1995 Last modified in Release 16, May 2003 Description Alkyl hydroperoxide reductase C22 protein (EC ) (SCRP-23) (Sulfate starvation- induced protein 8) (SSI8). Gene name(s) AHPC OR B0605 OR C0694 OR Z0749 OR ECS0644 OR SF0524 From Escherichia coli. [TaxID: 562]562 Taxonomy Bacteria; Proteobacteria; Gammaproteobacteria; Enterobacteriales; Enterobacteriaceae; Escherichia.  MAPPING ON GEL. MEDLINE= ; PubMed= ;[NCBI, ExPASy, EBI, Israel, Japan] Pasquali C., Frutiger S., Wilkins M.R., Hughes G.J., Appel R.D., Bairoch A., Schaller D., Sanchez J.-C., Hochstrasser D.F.; "Two-dimensional gel electrophoresis of Escherichia coli homogenates: the Escherichia coli SWISS-2DPAGE database."; Electrophoresis 17: (1996).NCBIExPASyEBIIsraelJapan
The Mechanism of Plaque Formation
Plaque as a Biofilm
Growth Changes & Cellular Fractionation Growth of F. nucleatum by continuous culture- maintain growth parameters while changing a single factor of interest. Growth conditions examined – growth rate growth temperature redox potential growth pH presence of chlorhexidine (antimicrobial) nutrient availability biofilm growth Sample preparation Sample preparation- a) consideration of mol. Wt. and pI. b) reduce the complexity of the protein mixture, (cytoplasmic and cell envelope). c) degradation of proteins by proteases d) removal of nucleic acids e) staining- determined by amount of protein f) protein contamination
Protein recovery-sequential protein extraction of the cell envelope of F. nucleatum ATCC Extract 1 - 8M Urea, 50mM DTT, 4% CHAPS Extract 2 – 7M Urea, 50mM DTT, 2M Thiourea, 4% CHAPS
Iso-electric focusing Iso-electric focusing - considerations for the novice salt, protein solubility and ampholyte concentration What size format? – 7cm, 11cm, 17cm pH range – 10 possible Protein concentration during rehydration. Active or passive rehydration
pH range and IPG size pH 3pH 10 pH 3pH10 11cm IPG 7cm IPG
pH 4 pH7 200 kDa 14.4 kDa 11cm IPG
39oC BHI CHXpH 8.0Control Master 11cm Cytosolic fraction of F. nucleatum pH 4-7