A variety of diseases including sickle cell anemia, beta- thalassemia, Tay-Sachs and phenylketonuria are the result of a single amino acid alteration in the structure of a particular protein or enzyme. Although we can determine the structure of a protein to atomic resolution, we still do not understand how, in detail, this structure is related to the function of the particular protein of enzyme. In order to understand the molecular basis of diseases, we need to elucidate at the molecular level the relationship between protein structure and function. Therefore, the long term goals of this project are to acquire a deeper understanding of the relationship between protein structure and function by using E. coli alkaline phosphatase as a model system. This enzyme catalyzes the nonspecific hydrolysis of phosphate esters, and is the model for the study of all alkaline phosphatases.
The specific aims of this proposal are to answer fundamental questions concerning the relationship between structure and function of alkaline phosphatase. We will concentrate on the molecular details of the catalytic mechanism, the mode by which information is passed between the subunits of the enzyme, and the function of the metals in this enzyme. We will use a variety of molecular biology techniques to create altered versions of the enzyme with single amino acid substitutions. Initially, work will concentrate on the analysis of mutants that have been already created. Selection of additional sites for amino acid substitutions will be based on all the biochemical and structural data currently available. Kinetic and biophysical methods such as stopped-flow kinetics, circular dichroism, NMR spectroscopy, and X-ray crystallography will be used to analyze the results of the amino acid substitutions. Correlations will be made between the functional changes induced by the amino acid substitution and the three-dimensional structure of the mutant enzymes. This work will not only be important for the understanding of this particular system, but more importantly for formulating general concepts about enzyme catalysis, cooperativity and the function of metals in proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM042833-02
Application #
3301743
Study Section
Physical Biochemistry Study Section (PB)
Project Start
1989-07-01
Project End
1993-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
2
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Boston College
Department
Type
Schools of Arts and Sciences
DUNS #
045896339
City
Chestnut Hill
State
MA
Country
United States
Zip Code
02467
Cockrell, Gregory M; Kantrowitz, Evan R (2012) Metal ion involvement in the allosteric mechanism of Escherichia coli aspartate transcarbamoylase. Biochemistry 51:7128-37
Wang, Jie; Kantrowitz, Evan R (2006) Trapping the tetrahedral intermediate in the alkaline phosphatase reaction by substitution of the active site serine with threonine. Protein Sci 15:2395-401
Stec, Boguslaw; Holtz, Kathleen M; Wojciechowski, Cheryl L et al. (2005) Structure of the wild-type TEM-1 beta-lactamase at 1.55 A and the mutant enzyme Ser70Ala at 2.1 A suggest the mode of noncovalent catalysis for the mutant enzyme. Acta Crystallogr D Biol Crystallogr 61:1072-9
Wang, Jie; Stieglitz, Kimberly A; Kantrowitz, Evan R (2005) Metal specificity is correlated with two crucial active site residues in Escherichia coli alkaline phosphatase. Biochemistry 44:8378-86
Zappa, S; Boudrant, J; Kantrowitz, E R (2004) Pyrococcus abyssi alkaline phosphatase: the dimer is the active form. J Inorg Biochem 98:575-81
Boulanger Jr, Robert R; Kantrowitz, Evan R (2003) Characterization of a monomeric Escherichia coli alkaline phosphatase formed upon a single amino acid substitution. J Biol Chem 278:23497-501
Wojciechowski, Cheryl L; Kantrowitz, Evan R (2003) Glutamic acid residues as metal ligands in the active site of Escherichia coli alkaline phosphatase. Biochim Biophys Acta 1649:68-73
Wojciechowski, Cheryl L; Cardia, James P; Kantrowitz, Evan R (2002) Alkaline phosphatase from the hyperthermophilic bacterium T. maritima requires cobalt for activity. Protein Sci 11:903-11
Wojciechowski, Cheryl L; Kantrowitz, Evan R (2002) Altering of the metal specificity of Escherichia coli alkaline phosphatase. J Biol Chem 277:50476-81
Holtz, K M; Stec, B; Myers, J K et al. (2000) Alternate modes of binding in two crystal structures of alkaline phosphatase-inhibitor complexes. Protein Sci 9:907-15

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