Gary Dmitrienko
Biography
Hospital-acquired infections (HAIs) are increasing with growing numbers of susceptible individuals in aging populations. So-called Gram-negative bacteria like Escherichia coli cause many thousands of HAIs each year. The beta-lactamsare the most important antibiotics for HAIs caused by these organisms. Since Gram-negative bacteria have become resistant to most other antibiotics, carbapenems (the most powerful beta-lactams) are now the most important treatment for these infections.
Gary Dmitrienko's research focuses on designing, creating and testing molecules that will block carbapenem-resistance mechanisms like NDM-1 and so enable carbapenems to kill resistant Gram-negative bacteria. Natural products with potent antibacterial and anticancer properties are also a major area of interest.
Research Interests
Bioorganic and medicinal chemistry related to antimicrobial and anticancer agents
Synthesis of heterocyclic and carbocyclic compounds
Mechanistic organic chemistry and biochemistry
Natural products chemistry and biochemistry
Education
1974, PhD, Organic Chemistry, University of Toronto, Canada
1970, BSc, Honours Chemistry, University of Toronto, Canada
Service
2012-2015, Member of the CIHR Industry-Partnered Collaborative Research Grant Selection Panel
2007, 2010, Member of the Pharmaceutical Sciences Operating Grant Selection Panel, Canadian Institutes for Health Research
Affiliations and Volunteer Work
Cross-appointed to the School of Pharmacy
Member, Waterloo Institute of Biochemistry & Molecular Biology
Member, Waterloo Centre for Microbial Research
Selected/Recent Publications
Assay for drug discovery: Synthesis and testing of nitrocefin analogues for use as β-lactamase substrates. Ghavami, A.; Labbé, G.; Brem, J.; Goodfellow, V. J.; Marrone, L., Tanner, C. A.; King, D. T., Lam, M.; Strynadka, N. C.; Pillai, D. R.; Siemann, S.; Spencer, J.; Schofield, C. J.; Dmitrienko, G. I. Anal. Biochem. 2015, 486, 75-7.
Arginine-containing peptides as potent inhibitors of VIM-2 metallo-β-lactamase. Rotondo, C. M.; Marrone, L.; Goodfellow, V. J., Ghavami, A.; Labbé, G.; Spencer, J.; Dmitrienko G. I.; Siemann, S. Biochim. Biophys. Acta. 2015, 1850, 2228-38.
Prekinamycin and an isosteric-isoelectronic analogue exhibit comparable cytotoxicity towards K562 human leukemia cells, Abbott, G.L.; Wu, X.; Zhao, Z.; Guo, L.; Birman, V.B; Hasinoff, B. B.; Dmitrienko, G.I. Med. Chem. Commun., 2014, 5, 1364-1370.
Cyclobutanone Analogues of b-Lactams Revisited: Insights Into Conformational Requirements for Inhibition of Serine- and Metallo-b-Lactamases. Johnson, J. W.; Gretes, M.; Goodfellow, V. J.; Marrone, L.; Heynen, M. L.; Strynadka, N. C. J.; Dmitrienko, G. I. J. Am. Chem. Soc. 2010, 132, 2558–2560.
Cyclobutanone Mimics of Penicillins: Effects of Substitution on Conformation and Hemiketal Stability. Johnson, J. W.; Evanoff, D. P.; Savard, M. E.; Lange, G.; Ramadhar, T. R.; Assoud, A.; Taylor, N. J.; Dmitrienko, G. I. J. Org. Chem. 2008, 73, 6970–6982.
In The News
Graduate studies
Not currently accepting applications for graduate students.