Zinc is widely recognized as an element that is essential to all forms of life, and especially that of humans. Thus, zinc plays important functions in numerous biological processes (e.g. carbohydrate, lipid, protein and nucleic acid synthesis, regulation and degradation; gene transcription; viral and immune phenomena) and is an indispensable element for effective growth and development, with deficiency resulting in organ malformations. The public health implications of zinc have, therefore, recently been strongly emphasized, thereby making the bioinorganic chemistry of zinc an essential and critical area of investigation. The principal aims of the proposed research are concerned with an effort to elucidate the biological chemistry of zinc that is performed by more than 300 enzymes, with representatives for each of the fundamental enzyme classes (oxidoreductases, transferases, hydrolases, lyases, isomerases, and ligases). Paramount to understanding the many roles of zinc in biological systems is a determination of how the chemistry of zinc is modulated by its coordination environment. A specific objective of the research proposed is to provide an understanding of the chemistry of zinc in a sulfur rich environment which is of relevance to enzymes such as liver alcohol dehydrogenase, the Ada DNA repair protein, and 5-aminolevulinate dehydratase. For example, the zinc enzyme 5-aminolevulinate dehydratase is necessary for the early steps of heme formation, and its inactivation by lead is one of the principal reasons why lead is poisonous to humans. The objectives of this proposal will be achieved by investigating synthetic analogues (i.e. small molecules that mimic both the structures and functions of the active sites of zinc enzymes) that are constructed using sulfur donor tripodal ligands to emulate the protein residues that coordinate to zinc in the enzymes. Elucidation of the roles that zinc plays in biological systems will provide the information that is necessary to allow for the possibility of rational therapeutic intervention.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM046502-13
Application #
7457728
Study Section
Macromolecular Structure and Function A Study Section (MSFA)
Program Officer
Fabian, Miles
Project Start
1993-08-01
Project End
2011-04-30
Budget Start
2008-07-01
Budget End
2011-04-30
Support Year
13
Fiscal Year
2008
Total Cost
$254,618
Indirect Cost
Name
Columbia University (N.Y.)
Department
Chemistry
Type
Other Domestic Higher Education
DUNS #
049179401
City
New York
State
NY
Country
United States
Zip Code
10027
Kreider-Mueller, Ava; Quinlivan, Patrick J; Owen, Jonathan S et al. (2017) Tris(2-mercaptoimidazolyl)hydroborato Cadmium Thiolate Complexes, [TmBut]CdSAr: Thiolate Exchange at Cadmium in a Sulfur-Rich Coordination Environment. Inorg Chem 56:4644-4654
Yurkerwich, Kevin; Quinlivan, Patrick J; Rong, Yi et al. (2016) Phenylselenolate Mercury Alkyl Compounds, PhSeHgMe and PhSeHgEt: Molecular Structures, Protolytic Hg-C Bond Cleavage and Phenylselenolate Exchange. Polyhedron 103:307-314
Chakrabarti, Neena; Ruccolo, Serge; Parkin, Gerard (2016) Cadmium Compounds with an [N3C] Atrane Motif: Evidence for the Generation of a Cadmium Hydride Species. Inorg Chem 55:12105-12109
Palmer, Joshua H; Parkin, Gerard (2015) Protolytic cleavage of Hg-C bonds induced by 1-methyl-1,3-dihydro-2H-benzimidazole-2-selone: synthesis and structural characterization of mercury complexes. J Am Chem Soc 137:4503-16
Kreider-Mueller, Ava; Quinlivan, Patrick J; Rong, Yi et al. (2015) Exchange of Alkyl and Tris(2-mercapto-1-t-butylimidazolyl)hydroborato Ligands Between Zinc, Cadmium and Mercury. J Organomet Chem 792:177-183
Kreider-Mueller, Ava; Quinlivan, Patrick J; Owen, Jonathan S et al. (2015) Synthesis and structures of cadmium carboxylate and thiocarboxylate compounds with a sulfur-rich coordination environment: carboxylate exchange kinetics involving tris(2-mercapto-1-t-butylimidazolyl)hydroborato cadmium complexes, [Tm(Bu(t))]Cd(O2CR). Inorg Chem 54:3835-50
Palmer, Joshua H; Parkin, Gerard (2015) Influence of Benzannulation on Metal Coordination Geometries: Synthesis and Structural Characterization of Tris(2-mercapto-1-methylbenzimidazolyl)hydroborato Cadmium Bromide, {[Tm(MeBenz)]Cd(?-Br)}2. J Mol Struct 1081:530-535
Rong, Yi; Palmer, Joshua H; Parkin, Gerard (2014) Benzannulated tris(2-mercapto-1-imidazolyl)hydroborato ligands: tetradentate ?4-S3H binding and access to monomeric monovalent thallium in an [S3] coordination environment. Dalton Trans 43:1397-407
Palmer, Joshua H; Parkin, Gerard (2014) Synthesis and Structural Characterization of 1-Arylimidazole-2-thiones and N,N'-Aryldiethoxyethylthioureas with Electronically Diverse Substituents: A Manifold of Hydrogen Bonding Networks. New J Chem 38:4071-4082
Palmer, Joshua H; Parkin, Gerard (2014) Synthesis and structural characterization of tris(2-mercapto-1-methylbenzimidazolyl)hydroborato cadmium halide complexes, {[Tm(MeBenz)]Cd(?-Cl)}2 and [Tm(MeBenz)]CdI: a rare example of cadmium in a trigonal bipyramidal sulfur-rich coordination environment Dalton Trans 43:13874-82

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