The opening of the 21st century has been heralded as a turning point in biomedical research. The completesequence and a dense map of the human genome, coupled with advanced genomics technologies holds thepromise of dramatically accelerating the understanding of human disease, which in turn is expected toaccelerate the pace of discovery of new therapeutics. Similarly, recent advances in synthetic organicchemistry have the potential to greatly improve chemical screening and compound optimization.In principle, these technical and conceptual advances have the potential to transform drug discovery. Inpractice, however, they have not yet done so. While emerging genomic and chemical technologies areavailable in isolation, they have not been creatively integrated into the drug discovery process. A key reasonhas been the lack of a concerted, interdisciplinary effort to merge the disciplines of genetics and chemistryinto a new conceptual framework.We propose here an ambitious plan to create a new approach to drug discovery involving four components. Component A (U54 Leadership) which includes the IRC Steering Committee. Component B (Discovery Pipeline). This component aims to develop a drug discovery pipeline based on the paradigm of phenotypic screening. This includes developing i) systematic high-throughput screening of phenotypic assays for cellular states based on gene-expression and imaging; ii) expanded libraries of DOS compounds to facilitate high-throughput screening, target identification and medicinal chemistry optimization; and iii)genomics-based approaches to predictive toxicology. Component C (Target ID).This component aims to develop systematic approaches to identifying the protein target of a small molecule based on i) techniques for affinity capture and proteomic analysis; ii) novel approaches using RNA inhibition (RNAi); and iii) novel computational approaches to recognize distinctive cellular signatures. Component D (Driving Medical Projects). To drive its development and test its utility, the new paradigm must be applied to specific biomedical problems. This component will undertake six demonstration projects.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Linked Specialized Center Cooperative Agreement (UL1)
Project #
1UL1RR024924-01
Application #
7466799
Study Section
Special Emphasis Panel (ZRR1-SRC (99))
Program Officer
Farber, Gregory K
Project Start
2007-09-20
Project End
2012-06-30
Budget Start
2007-09-20
Budget End
2008-06-30
Support Year
1
Fiscal Year
2007
Total Cost
$352,307
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
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