This revised application describes experiments designed to clarify therole of a protein produced by E. corrodens which has been implicated as a toxin with effects on human epithelial cells, fibroblasts, and HL60 cells.A monoclonal antibody has been identified which blocks the toxic activities of the organism, and that Mab reacts with an approximately 72Kd molecule produced by E. corrodens. Interestingly, the Mab also cross-reacts with a protein of apparently 140Kd produced by S. sanguis. Antisera reactive to the 140Kd protein also react with the E. corrodens 72Kd molecule. The experimental plan described in this application is to clone and inactivate the gene encoding the 72Kd molecule from E. corrodens and evaluate the effects of its inactivation on the toxicity in various cell culture systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Small Research Grants (R03)
Project #
1R03DE011186-01A1
Application #
2132357
Study Section
NIDCR Special Grants Review Committee (DSR)
Project Start
1995-03-01
Project End
1997-02-28
Budget Start
1995-03-01
Budget End
1996-02-29
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Oklahoma Health Sciences Center
Department
Biochemistry
Type
Schools of Dentistry
DUNS #
937727907
City
Oklahoma City
State
OK
Country
United States
Zip Code
73117