The length of telomeres and its control mechanism by telomerases decide the lifetime of cells. Understanding how this mechanism works will provide deeper insight on how to control the proliferation of tumor cells and may have direct impact on anticancer drug designs. Formation of G-quartets by G-rich sequences inhibits extension of the DNA sequence by telomerase in vitro. The inhibitor that is able to bind quadruplexes may therefore serve as a potential agent to inhibit the proliferation of tumor cells. In order to understand the details in the interactions between the inhibitor and the quadruplex, their complex structure is being studied through NMR spectroscopies. Solving the NMR structure depends on access to Computer Graphics Laboratory resources: assignments are aided by the software packages, NMRPipe and Sparky, structural calculations depend on DYANA and MARDIGRAS, visualization of structures will be done using MidasPlus and structure refinement will include back calculations through CORMA.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
3P41RR001081-22S1
Application #
6220359
Study Section
Project Start
1999-07-01
Project End
2000-06-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
22
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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