?Fat? and ?Slim? Nucleosides and Nucleotides as Potential Aticancer and Antiviral Agents: These novel ring-expanded (?fat?) and ring-contracted (?slim?) nucleoside analogues, designed and synthesized in this lab, are potential chain-terinators of nucleic acid synthesis when incorporated into a tumor or viral DNA/RNA during transcription (or reverse transcription in case of retroviruses including HIV that causes AIDS). Mode of chain termination, and hence the viral or tumor replication, is believed to be the base-mispairing accompanied by considerable deviation of the base-sugar bond from the natural array. In addition, because of their unique structural, spatial, and conformational characteristics and constraints, ?fat? and ?slim? nucleosides/-tides are excellent probes for nucleic acid metabolism, structure, and function. While we use EI/CI/FAB Mass Spectrometry for routine structural analyses of small molecules, the MALDI TOF mass spectrometer is necessary for the molecular weight determination and purity of oligonucleotides derived from or incorporated with ?fat? or ?slim? nucleotides.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
3P41RR000480-28S1
Application #
6258822
Study Section
Project Start
1997-06-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
28
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Michigan State University
Department
Type
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
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