Among its many functions, TGF-beta1 up- and down-regulates proliferation of HIV infected cells. We have recently completed a determination of the three dimensional structure of TGF-beta1 in solution. The overall structure is similar to the independently determined x-ray structure of TGF-beta1. However, there are significant differences in the local structures of the two proteins, involving residues 69-74 and hydrophobic sidechains of residues in the ranges 24-33 and 88-102. We have analyzed the x-ray and NMR data with the goal of deriving a structure based explanation for the differences in the function of the two TGF-beta isoforms. The significance of this project arises from the unique, detailed structural information that we have obtained about TGF-beta1 in solution. This information will contribute improved understanding of the structure/function relationships of the family of TGF-beta proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Intramural Research (Z01)
Project #
1Z01DE000645-02
Application #
2572419
Study Section
Special Emphasis Panel (ODIR)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1996
Total Cost
Indirect Cost
Name
National Institute of Dental & Craniofacial Research
Department
Type
DUNS #
City
State
Country
United States
Zip Code