At the molecular level, many diseases such as cancer and diabetes involve abnormal protein-protein interactions. Contrary to traditional thought, new research suggests that small molecules can antagonize specific protein-protein interactions. This represents a new paradigm in the pharmaceutical industry because protein-protein interactions are an unexplored context for lead compound discovery. Funding from National Institutes of Health will foster the research proposed here. This work serves multiple purposes. First, significant progress will be made towards the development of a drug that blocks the interaction of the tumorigenic cytokine Interleukin-2 (IL-2), with its receptor, IL-2Ralpha. Second, we will gain new insights into the nature of small molecule binding at protein interfaces. Third, we will develop a rapid and parallel method for discovering small-molecule/protein interactions across a broad range of targets.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
3F32CA093177-04S1
Application #
6915886
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Program Officer
Lohrey, Nancy
Project Start
2002-06-19
Project End
2004-09-30
Budget Start
2003-12-01
Budget End
2004-09-30
Support Year
4
Fiscal Year
2004
Total Cost
$13,741
Indirect Cost
Name
University of California San Francisco
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Thanos, Christopher D; DeLano, Warren L; Wells, James A (2006) Hot-spot mimicry of a cytokine receptor by a small molecule. Proc Natl Acad Sci U S A 103:15422-7