The reaction of physiological significance catalyzed by the carbonic anhydrases is the hydration of carbon dioxide: CO2 + H2O yields or reversible action HCO3 + H+. This catalysis requires attack on CO2 by zinc-bound hydroxide followed by proton shuttle, to regenerate the zinc- bound hydroxide. The unifying goal of this proposal is to understand the catalytic mechanism of the carbonic anhydrases with emphasis on the rate- limiting proton transfer steps. A concurrent goal is to apply Marcus rate theory both to understand the catalytic mechanism of carbonic anhydrase and to elucidate the significance of the parameters of the Marcus theory to proton transfer in an enzyme. We plan to use site-specific mutagenesis and chemical modification to vary the location in the active-site cavity of the intramolecular proton shuttle and the pK of the zinc-bound water. For this purpose we have expression systems for three isozymes of carbonic anhydrase (II, III, and V) giving us a thousand-fold range of catalytic activities in the wild-type enzymes and a range and geometries for study. For each of these isozymes a crystal structure is available, and further structural implications of strategic mutations will be determined by x-ray crystallography. Stopped-flow and 18 O exchange between CO2 and water measured by mass spectrometry will be used to obtain rate constants for intramolecular proton transfer. Solvent hydrogen isotope effects will be measured to determine the rate-limiting nature of the proton transfer. We will evaluate the relationship between the basicity of the zinc-bound water and the rate of its nucleophilic attack on CO2 in carbonic anhydrase and mutants. We will apply Marcus rate theory to determine and interpret the intrinsic energy barriers for proton transfer and relate them to the structural and chemical features of the active site of carbonic anhydrase. The overall usefulness of the marcus theory to understanding proton transfer in carbonic anhydrase will be evaluated.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM025154-22
Application #
2900512
Study Section
Biochemistry Study Section (BIO)
Project Start
1978-04-01
Project End
2000-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
22
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Florida
Department
Pharmacology
Type
Schools of Medicine
DUNS #
073130411
City
Gainesville
State
FL
Country
United States
Zip Code
32611
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Zhu, Wen; Easthon, Lindsey M; Reinhardt, Laurie A et al. (2016) Substrate Binding Mode and Molecular Basis of a Specificity Switch in Oxalate Decarboxylase. Biochemistry 55:2163-73
Mahon, Brian P; Bhatt, Avni; Socorro, Lilien et al. (2016) The Structure of Carbonic Anhydrase IX Is Adapted for Low-pH Catalysis. Biochemistry 55:4642-53
Pinard, Melissa A; Mahon, Brian; McKenna, Robert (2015) Probing the surface of human carbonic anhydrase for clues towards the design of isoform specific inhibitors. Biomed Res Int 2015:453543
Aggarwal, Mayank; Chua, Teck Khiang; Pinard, Melissa A et al. (2015) Carbon Dioxide ""Trapped"" in a ?-Carbonic Anhydrase. Biochemistry 54:6631-8
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Mahon, Brian P; Pinard, Melissa A; McKenna, Robert (2015) Targeting carbonic anhydrase IX activity and expression. Molecules 20:2323-48
Mahon, Brian P; Lomelino, Carrie L; Salguero, Antonieta L et al. (2015) Observed surface lysine acetylation of human carbonic anhydrase II expressed in Escherichia coli. Protein Sci 24:1800-7
Boone, Christopher D; Rasi, Valerio; Tu, Chingkuang et al. (2015) Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase II. FEBS J 282:1445-57
Mahon, Brian P; Díaz-Torres, Natalia A; Pinard, Melissa A et al. (2015) Activity and anion inhibition studies of the ?-carbonic anhydrase from Thiomicrospira crunogena XCL-2 Gammaproteobacterium. Bioorg Med Chem Lett 25:4937-40

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