Stephen L. Bearne
PhD (Toronto), MDCM (McGill)
Professor and HeadCross-appointment with the Department of Chemistry
Department member since 1996
Enzyme Catalysis and Chemical Biology
DO YOU HAVE A PASSION FOR BIOLOGICAL CHEMISTRY, ENZYME MECHANISMS, & ENZYME CATALYSIS?
We do! Our research program has three major goals: (1) to understand the nature of the protein-ligand interactions that contribute to stabilization of reactive intermediates and transition states, relative to the ground state, (2) using this information to engineer new catalytic activities and develop tools for identification of specific enzymes in complex proteomes, and (3) to understand the chemical mechanism of enzymes that are of therapeutic interest.
FUNDAMENTAL ENZYMOLOGY: Mechanism, Structure, Function, & Evolution
Mandelate racemase (MR) is a member of the enolase superfamily of enzymes and catalyzes the rapid carbon-hydrogen bond cleavage of a carbon acid substrate with a relatively high pKa value. We are studying MR as a paradigm for understanding how enzymes overcome the problem of carbon acidity, a common feature of many biological reactions. Using new transition state analogue inhibitors that we have developed, in combination with site-directed mutagenesis and biophysical techniques, we are studying the nature of the protein-ligand interactions that stabilize the altered substrate in the transition state. We are also conducting protein engineering and directed evolution to alter the substrate specificity of MR, and we are conducting investigations to understand the evolution of complexity in enzyme structure.
ENZYME TARGETS IN DISEASE: Neglected Tropical Diseases, Cancer, & Antibiotics
The enzyme cytidine 5'-triphosphate synthase (CTPS) belongs to a family of enzymes known as the glutamine amidotransferases and catalyzes the conversion of UTP to CTP. Inhibition of CTPS activity could offer a means of ameliorating a variety of diseases, including cancer, viral infections, and protozoal infections. Our goals are to understand how the allosteric effector, GTP acts to promote glutamine hydrolysis, and to develop specific inhibitors of GTP-dependent activation of CTPS. We are also studying the enzymology of racemases with the goal of developing specific and potent inhibitors. Racemases under investigation include the prostate cancer biomarker alpha-methylacyl-CoA racemase, and those racemases involved in generating D-amino acids (antibacterial targets).
Studies are focused on developing reagents for proteomic profiling of enzymatic activities.
DEVELOPING YOUR TOOL BOX
Graduate training in the Bearne Lab is designed to develop your critical and analytical thinking skills. Students have the opportunity to develop technical skills in a vast number of areas, including organic synthesis and protein chemistry, physical organic laboratory techniques, molecular modeling, enzyme kinetics, CD spectroscopy, microbiology, molecular biology, site-directed mutagenesis, isothermal titration calorimetry, macroion mobility spectrometry, NMR spectroscopy, chromatography (e.g.,HPLC & FPLC), and proteomics. This broad set of techniques is a great asset for students interested in exploring the exciting frontiers at the interface of modern biology and chemistry.
We thank the following agencies for past and present grants in aid of our research:
NSERC, CIHR, NSHRF, the Beatrice Hunter Cancer Research Institute, the Dalhousie Medical Research Foundation, and the Prostate Cancer Research Foundation
enzymology, enzyme kinetics and inhibition, chemical biology, organic synthesis, proteomics. Techniques: site-directed mutagenesis, protein & modification, HPLC, FPLC, CD, UV-vis, NMR, 2D gel electrophoresis, ITC, macroion mobility spectrometry
|Greg McCluskey||Ph.D. (Biochemistry)|
|Dr. Colin Douglas||University of Toronto|
|Dr. Himank Kumar||Visvesvaraya National Institute of Technology (VNIT)|
|Philipp Knopf||Biochemistry (2017)|
- Bearne, S.L.*, (2017) The interdigitating loop of the enolase superfamily as a specificity binding determinant or ‘flying buttress’ Biochim. Biophys. Acta :in press. [PubMed]
- Bhar, P., and Bearne, S.L.*, (2017) Unexpected side product formed during LDA-induced phosphonylation of uridine Chem. Lett. 46:in press.
- Harty, M., and Bearne, S.L.*, (2016) Measuring Benzohydroxamate Complexation with Mg2+, Mn2+, Co2+, and Ni2+ Using Isothermal Titration Calorimetry J. Therm. Anal. Calorim. 123:2573–2582
- Pal, M., Khanal, M., Marko, R., Thirumalairajan, S., and Bearne, S.L.*, (2016) Rational design and synthesis of substrate‐product analogue inhibitors of α‐methylacyl‐coenzyme A racemase from Mycobacterium tuberculosis Chem. Commun. 52:2740-2743
- McCluskey, G.D., Mohamady, S., Taylor, S.D., Bearne, S.L., (2016) Exploring the Potent Inhibition of CTP Synthase by Gemcitabine-5(prime)-Triphosphate ChemBioChem 17:2240-2249 [PubMed]
- Nagar, M., Wyatt, B.N., St. Maurice, M., Bearne, S.L.*, (2015) Inactivation of Mandelate Racemase by 3-Hydroxypyruvate Reveals a Potential Mechanistic Link between Enzyme Superfamilies Biochemistry 54:2747-2757 [PubMed]
- Nagar, M., Bearne, S.L.*, (2015) An Additional Role for the Brønsted Acid-Base Catalysts of Mandelate Racemase in Transition State Stabilization Biochemistry 54:6743-6752 [PubMed]
- Bearne, S.L.*, (2015) Comment on “A Better Magnetic Stir Bar Retriever” J. Chem. Educ. 92:1777-1777 [Article]
- Bearne, S.L.*, (2014) Illustrating the effect of pH on enzyme activity using Gibbs energy profiles J. Chem. Educ. 91:84-90
- Harty, M., Nagar, M., Atkinson, L., LeGay, C.M., Derksen, D.J.*, Bearne, S.L.*, (2014) Inhibition of serine and proline racemases by substrate-product analogues Bioorg. Med. Chem. Lett. 24:390-393. [PubMed]
- Pal, M., and Bearne, S.L.*, (2014) Inhibition of glutamate racemase by substrate-product analogues Bioorg. Med. Chem. Lett. 24:1432-1436 [PubMed]
- Nagar, M., Lietzan, A.D., St. Maurice, M., Bearne, S.L.*, (2014) Potent inhibition of mandelate racemase by a fluorinated substrate-product analogue with a novel binding mode Biochemistry 53:1169-1178 [PubMed]
- Pal, M., and Bearne S.L.*, (2014) Synthesis of coenzyme A thioesters using methyl acyl phosphates in an aqueous medium Org. Biomol. Chem. 12:9760-9763 [PubMed]
- Bearne, S.L.*, (2012) Illustrating enzyme inhibition using free energy profiles J. Chem. Educ. 89:732-737.
- Lietzan, A.D., Nagar, M., Pellmann, E.A., Bourque, J.R., Bearne, S.L., St. Maurice, M.*, (2012) Structure of mandelate racemase with bound intermediate analogues benzohydroxamate and cupferron. Biochemistry 51 (6):1160-1170 [PubMed]
- Steeves, C.H., Potrykus, J., Barnett, D.A., and Bearne, S.L.*, (2011) Oxidative stress response in the opportunistic oral pathogen Fusobacterium nucleatum Proteomics 11:2027-2037. [PubMed]
- Steeves, C.H., and Bearne, S.L.*, (2011) Activation and inhibition of CTP synthase from Trypanosoma brucei, the causative agent of African sleeping sickness Bioorg. Med. Chem. Lett. 21:5188-5190. [PubMed]
- Nagar, M., Narmandakh, A., Khalak, Y., Bearne, S.L.*, (2011) Redefining the minimal substrate tolerance of mandelate racemase. Racemization of trifluorolactate. Biochemistry 50(41):8846-8852 [PubMed]
- Narmandakh, A., and Bearne, S.L.*, (2010) Purification of recombinant mandelate racemase: Improved catalytic activity. Protein Expr. Purif. 69:39-46. [PubMed]
- Ouazia, D., and Bearne, S.L.*, (2010) A continuous assay for alpha-methylacyl-coenzyme A racemase using circular dichroism. Anal. Biochem. 398:45-51. [PubMed]
- Roy, A.C., Lunn, F.A., and Bearne, S.L., (2010) Inhibition of CTP synthase from Escherichia coli by xanthines and uric acids Bioorg. Med. Chem. Lett. 20:141-144. [PubMed]
- Thirumalairajan, S., Mahaney, B., and Bearne, S.L.*, (2010) Interrogation of the active site of OMP decarboxylase from Escherichia coli with a substrate analogue bearing an anionic group at C6 Chem. Comm. 46:3158-3160. [PubMed]
- Potrykus, J., Flemming, J., and Bearne, S.L.*, (2009) Kinetic Characterization and Quaternary Structure of Glutamate Racemase from the Periodontal Anaerobe Fusobacterium nucleatum Arch. Biochem. Biophys. 491:16-24. [PubMed]
- Bourque, J.R., and Bearne, S.L.*, (2008) Mutational Analysis of the Active Site Flap (20s Loop) of Mandelate Racemase. Biochemistry 47:566-578. [PubMed]
- Lunn, F.A., MacDonnell, J.E., and Bearne, S.L.*, (2008) Structural requirements for the activation of Escherichia coli CTP synthase by the allosteric effector GTP are stringent, but requirements for inhibition are lax. J. Biol. Chem. 283:2010-2020. [PubMed]
- Taylor, S.D.*, Mirzaei, F., and Bearne, S.L., (2008) Bismethylene Triphosphate Nucleotides of Uridine 4-Phosphate Analogues: A New Class of Anionic Pyrimidine Nucleotide Analogues J. Org. Chem. 73:1403-1412. [PubMed]
- Lunn, F.A., MacLeod, T.J., Bearne, S.L.*, (2008) Mutational analysis of conserved glycine residues 142, 143 and 146 reveals Gly-142 is critical for tetramerization of CTP synthase from Escherichia coli. Biochem. J. 412:113-121. [PubMed]
- Potrykus, J., White, R.L.*, and Bearne, S. L.*, (2008) Proteomic Investigation of Amino Acid Catabolism in the Indigenous Gut Anaerobe Fusobacterium varium. Proteomics 8:2691-2703. [PubMed]
- Taylor, S.D.*, Lunn, F.A., and Bearne, S.L.*, (2008) Ground State, Intermediate, and Multivalent Nucleotide Analogue Inhibitors of Cytidine 5'-Triphosphate Synthase ChemMedChem 3:1853-1857. [PubMed]
- Bourque, J.R., Burley, R.K.M., and Bearne, S.L.*, (2007) Intermediate analogue inhibitors of mandelate racemase: N-Hydroxyformanilide and cupferron. Bioorg. Med. Chem. Lett. 17:105-108. [PubMed]
- Potrykus, J., Mahaney, B., White, R.L.*, and Bearne, S.L.*, (2007) Proteomic investigation of glucose metabolism in the butyrate-producing gut anaerobe Fusobacterium varium. Proteomics 7:1839-1853. [PubMed]
- Taylor, S.D.*, Mirzaei, F., and Bearne, S.L., (2006) An unsymmetrical approach to the synthesis of bismethylene triphosphate analogues. Org. Lett. 8:4243-4246. [PubMed]
- MacLeod, T.J., Lunn, F.A., and Bearne, S.L.*, (2006) The role of lysine residues 297 and 306 in nucleoside triphosphate regulation of E. coli CTP synthase. Inactivation by 2',3'-dialdehyde ATP and mutational analyses. Biochim. Biophys. Acta 1764:199-210. [PubMed]
- Taylor, S.D.*, Mirzaei, F., Sharifi, S., and Bearne, S.L., (2006) Synthesis of Methylene- and Difluoromethylenephosphonate Analogs of Uridine-4-Phosphate and 3-Deazauridine-4-Phosphate. J. Org. Chem. 71:9420-9430. [PubMed]
- O'Malley, P.G.P., Sangster, S.M., Abdelmagid, S.A., Bearne, S.L. and Too, C.K.L.*, (2005) Characterizaion of a novel, cytokine-inducible carboxypeptidase-D isoform in hematopoietic tumor cells. Biochem J. 390:665-673. [PubMed] [Article]
- Bearne, S.L.*, and Spiteri, R.J., (2005) Reduction of intrinsic kinetic and thermodynamic barriers for enzyme-catalysed proton transfers from carbon acid substrates. J. Theor. Biol. 233:563-571. [PubMed]
- Siddiqi, F., Bourque, J.R., Jiang, H., Gardner, M., St. Maurice, M., Blouin, C., and Bearne, S.L.*, (2005) Perturbing the Hydrophobic Pocket of Mandelate Racemase To Probe Phenyl Motion during Catalysis. Biochemistry 44:9013-9021. [PubMed]
- Brosseau, C.L., St. Maurice, M., Bearne, S.L., and Roscoe, S.G.*, (2005) Electrochemical quartz crystal nanobalance (EQCN) studies of the adsorption behaviour of an enzyme, mandelate racemase, and its substrate, mandelic acid, on Pt. Electrochim. Acta 50:1289-1297.
- Burley, R.K.M., and Bearne, S.L.*, (2005) Inhibition of mandelate racemase by the substrate-intermediate-product analogue 1,1-diphenyl-1-hydroxymethylphosphonate. Bioorg. Med. Chem. Lett. 15:4342-4344. [PubMed]
- Lunn, F.A., and Bearne, S.L.*, (2004) Alternative Substrates for Wild-type and L109A E. coli CTP Synthases. Kinetic Evidence for a Constricted Ammonia Tunnel. Eur. J. Biochem. 271:4204-4212. [PubMed]
- MacDonnell, J.E., Lunn, F.A., and Bearne, S.L.*, (2004) Inhibition of E. coli CTP synthase by the positive allosteric effector GTP. Biochim. Biophys. Acta 1699:213-220. [PubMed]
- St. Maurice, M., and Bearne, S.L.*, (2004) Hydrophobic Nature of the Active Site of Mandelate Racemase. Biochemistry 43:2524-2532. [PubMed]
- Iyengar, A., and Bearne, S.L.*, (2003) Aspartate-107 and leucine-109 facilitate efficient coupling of glutamine hydrolysis to CTP synthesis by Escherichia coli CTP synthase. Biochem. J. 369:497-507. [PubMed]
- Simard. D., Hewitt, K.A., Lunn, F., Iyengar, A., and Bearne, S.L.*, (2003) Limited proteolysis of Escherichia coli cytidine 5'-triphosphate synthase. Identification of residues required for CTP formation and GTP-dependent activation of glutamine hydrolysis. Eur. J. Biochem. 270:2195-2206. [PubMed]
- St. Maurice, M., Bearne, S.L.*, Lu, W., and Taylor, S.D., (2003) Inhibition of mandelate racemase by alpha-fluorobenzylphosphonates. Bioorg. Med. Chem. Lett. 13:2041-2044. [PubMed]
- St. Maurice, M., and Bearne, S.L.*, (2002) Kinetics and Thermodynamics of Mandelate Racemase Catalysis. Biochemistry 41:4048-4058. [PubMed]
- Iyengar, A., and Bearne, S.L.*, (2002) An assay for cytidine 5'-triphosphate synthetase glutaminase activity using high performance liquid chromatography. Anal. Biochem. 308:396-400. [PubMed]
- Bearne, S.L.*, White, R.L.*, MacDonnell, J.E., Bahrami, S., and Gronlund, J., (2001) Purification and characterization of beta-methylaspartase from Fusobacterium varium. Mol. Cell. Biochem. 221:117-126. [PubMed]
- Bearne, S.L.*, Hekmat, O., and MacDonnell, J.E., (2001) Inhibition of Escherichia coli CTP synthase by glutamate gamma-semialdehyde and the role of the allosteric effector GTP in glutamine hydrolysis. Biochem. J. 356:223-232. [PubMed]
- St. Maurice, M., and Bearne, S.L.*, (2000) Reaction intermediate analogues for mandelate racemase: interaction between Asn 197 and the alpha-hydroxyl of the substrate promotes catalysis. Biochemistry 39:13324-13335. [PubMed]
- Bearne, S.L.*, and Blouin, C., (2000) Inhibition of Escherichia coli glucosamine-6-phosphate synthase by reactive intermediate analogues. The role of the 2-amino function in catalysis. J. Biol. Chem. 275:135-140. [PubMed]
- Bearne, S.L.*, St. Maurice, M., and Vaughan, M.D., (1999) An assay for mandelate racemase using high-performance liquid chromatography. Anal. Biochem. 269:332-336. [PubMed]