With support from the Chemistry of Life Processes Program in the Chemistry Division of the National Science Foundation, Professors Paramjit Arora and Richard Bonneau, of the Departments of Chemistry and Biology at New York University, will study synthetic mimics of protein subdomains that can modulate the function of chosen proteins. Targets include nonpeptidic oligomers that mimic the alpha-helical conformation and display protein-like functionality. The oxopiperazine helix mimetic oligomers will be synthesized using standard procedures from natural and nonnatural amino acids. The researchers will develop experimental and computational approaches for screening libraries of nonpeptidic helix mimetics against model protein targets to identify high affinity, selective ligands. They will implement computational tools that can accurately predict local conformations of nonpeptidic oligomers and estimate optimum constructs for chosen protein receptors. Furthermore, they will explore the potential of oligooxopiperazines to target the DNA major groove. With this award, these researchers will demonstrate computational and synthetic design principles, and synthetic organic methods to develop new classes of biologically active compounds. This approach will result in biomimetic oligomers that are anticipated to become valuable reagents for the biomedical community. This work represents a new direction in bioorganic chemistry: providing access to nonpeptidic oligomers that assemble from amino acids while preserving the chiral backbone and side chain functionality.

Students engaged in this work will gain broad experience in molecular design, conformational analysis, synthesis, and biochemistry. Members of the research team will include graduate and undergraduate students, drawing also from underrepresented groups. Students trained on the project may go on to careers in the pharmaceutical or biotechnology industry, or academia, and will thus contribute to the US scientific endeavor and the economy. Professors Arora and Bonneau will continue to engage educators that teach at predominantly minority institutions by organizing workshops that discuss research and teaching advances at the interface of chemistry and biology.

Project Report

With this award, the PI Arora and Co-PI Bonneau designed nonpeptidic scaffolds that mimic the alpha-helical conformation and display protein-like functionality. We designed, synthesized and evaluated a nonpeptidic alpha-helix mimetic to target chosen protein-protein interactions. The oxopiperazine helix mimetics were synthesized using standard procedures from natural and nonnatural amino acids and shown to target the chosen protein receptors in cell free, cell culture and animal models. The results represent a key advance in the field of protein-protein interaction inhibition by small molecule helix mimics in vivo. Importantly, the project yielded a computational approach for screening libraries of nonpeptidic helix mimetics against model protein targets to identify high affinity, selective ligands. Students engaged in this work gained broad experience in molecular design, conformational analysis, synthesis, and biochemistry. Members of the research team included graduate and undergraduate students, drawing also from underrepresented groups. Students trained on the project may go on to careers in the pharmaceutical or biotechnology industry, or academia, and will thus contribute to the US scientific endeavor and the economy. Professors Arora and Bonneau engaged educators that teach at predominantly minority institutions (Spelman College) by organizing workshops that discuss research and teaching advances at the interface of chemistry and biology.

Agency
National Science Foundation (NSF)
Institute
Division of Chemistry (CHE)
Application #
1151554
Program Officer
David Rockcliffe
Project Start
Project End
Budget Start
2012-04-01
Budget End
2015-03-31
Support Year
Fiscal Year
2011
Total Cost
$360,000
Indirect Cost
Name
New York University
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10012