- Protein identification in complex mixtures (biomarker discovery)
- Post-translational modification analysis (phosphorylation, N-acetylation, glycosylation etc.)
- Quantitative proteomics
- MS-based on stable isotope labeling method
- Label-free (MS1 peak integration/intensity, counting MS2 spectra)
- Identification of interacting proteins (protein complexes analysis, protein-protein interactions)
- DNA-, RNA- protein interactions
- Targeted proteomics (PRMs)
- Multiple stage fragmentation capabilities: HCD, CID and ETD
- Proteomic based on MS3 level [tandem mass tag (TMT), Isobaric tags for relative and absolute quantitation (iTRAQ), phosphoproteomics, cross-linked peptides]
Services
The Biological John L. Holmes Mass Spectrometry Facility at the University of Ottawa provides support for high quality research activities and enhances the educational experience of students.
Proteomics
Metabolomics
- Mass Determination
- Natural abundance of isotopes
- Structural characterization/elucidation (full scan and fragmentation pattern)
- Quantification
- Targeted and untargeted metabolomics
- Protein-ligand interaction
Bioinformatics
- Protein and peptide analysis using bottom-up proteomics
- Identification and relative label-free quantification of proteins and peptides (MaxQuant and Proteome Discoverer)
- Identification of various post-translational and chemical protein modifications (phosphoproteins, protein acetylation, biotinylation and others)
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Statistical analysis of proteomics data
- One-group (correlation analysis), two-group (t-test), and multi-group (ANOVA) hypothesis testing
- Supervised and unsupervised dimension reduction (PCA, PLS-DA)
- Hierarchical clustering
Contact Us
Biological facility
Zoran Minic
[email protected]
Marion Hall - Room 02
Ottawa, ON K1N 1A2
Tel: 613-562-5800 ext. 1626