This proposal describes two projects involving structure determinations of proteins that are drug design targets. One of these, Microsomal Triglyceride Transfer Protein (MTP), is a protein involved in the transport of lipids and phospholipids between membranes in the liver and intestine. It is proposed that inhibitors of MTP will block the uptake of cholesterol in the liver and intestine and provide dramatically more effective cholesterol lowering therapies. The other project involves _-glucuronidase, which cleaves _-glucuronic acid from glycosaminoglycans and is an essential enzyme for the normal turnover of these extracellular matrix components. _-glucuronidase and other lysosomal enzymes are released into the synovial fluid in inflammatory joint diseases such as rheumatoid arthritis where they contribute to the symptoms. Efforts are underway to cocrystallize both of these enzymes in the presence of inhibitors as part of an interactive drug design project.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-20
Application #
6119389
Study Section
Project Start
1999-03-01
Project End
2000-04-14
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
20
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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