Tooth enamel is secreted as a protein matrix which is removed as the enamel matures. The largest fraction of the protein matrix consists of amelogenins, which are selectively removed from the enamel as maturation progresses. This processing of amelogenins is important for regulating crystal growth in the mineralizing enamel matrix. The overall objective in this proposal is to better understand amelogenin processing by identifying and characterizing amelogeninases in the developing enamel matrix. The specific hypothesis to be tested is that a serine proteinase, expressed by ameloblasts, is responsible for the hydrolysis of amelogenin protein in the developing enamel matrix.
The specific aims are: 1) to isolate and purify the serine proteinase in enamel which actively hydrolyzes amelogenin; 2) to characterize the amelogeninase for substrate specificity, pH optima and thermal stabilities; 3) to determine the specific cleavage sites of the amelogeninase by using purified 25,000 MW amelogenin as a susbstrate; 4) to amplify, clone and sequence the cDNA(s) from bovine enamel organ mRNA which contains the conserved active site for a serine proteinase; 5) to clone a full-length cDNA for the serine proteinase/amelogeninase from a bovine enamel organ lambda phage cDNA library and to begin in situ hybridization studies. Purification and characterization of the serine proteinase/amelogeninase will be completed by isoelectric focusing, gel electrophoresis and column chromatography. Specificity of the amelogeninase will be determined by hydrolysis of a purified amelogenin substrate. The cDNA for the serine proteinase will be cloned to allow comparisons between the initially expressed mRNA transcript and the active form of the proteinase present in the enamel matrix. These studies to identify and characterize the serine proteinase/amelogeninase in developing enamel will lead to a better understanding of the mechanisms by which amelogenesis occurs. They will also further our understanding of defects which occur in enamel formation, such as in enamel fluorosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE010614-05
Application #
2331324
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Project Start
1994-02-01
Project End
1999-01-31
Budget Start
1997-02-01
Budget End
1999-01-31
Support Year
5
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Other Health Professions
Type
Schools of Dentistry
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Li, W; Machule, D; Gao, C et al. (1999) Activation of recombinant bovine matrix metalloproteinase-20 and its hydrolysis of two amelogenin oligopeptides. Eur J Oral Sci 107:352-9
Den Besten, P K; Punzi, J S; Li, W (1998) Purification and sequencing of a 21 kDa and 25 kDa bovine enamel metalloproteinase. Eur J Oral Sci 106 Suppl 1:345-9
Punzi, J S; DenBesten, P K (1995) Purification of nonamelogenin proteins from bovine secretory enamel. Calcif Tissue Int 57:379-84