Fluorescent pteridine-based nucleoside analogs that can be site-specifically incorporated into DNA oligonucleotides through a phosphodiester linkage have been developed and patented. The fluorescence properties of a series of these compounds have been characterized and potential applications are being investigated. These new fluorophores are promising probes for the study of protein/DNA interactions, because they are not attached to DNA externally and they do not appear to disrupt the tertiary structure of DNA. The utility of these fluorophores as hybridization probes has been investigated and patented. Collaborative studies to investigate other applications for these new probes are also ongoing and the Imaging Probe Development Center (IPDC), which is part of the NIH Roadmap Initiative, has selected these compounds for development.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01SC010090-11
Application #
7594802
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
11
Fiscal Year
2007
Total Cost
$121,957
Indirect Cost
Name
National Cancer Institute Division of Clinical Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Hawkins, Mary E (2007) Synthesis, purification and sample experiment for fluorescent pteridine-containing DNA: tools for studying DNA interactive systems. Nat Protoc 2:1013-21
Turingan, Rosemary S; Liu, Cuihua; Hawkins, Mary E et al. (2007) Structural confirmation of a bent and open model for the initiation complex of T7 RNA polymerase. Biochemistry 46:1714-23
Hawkins, Mary E; Balis, Frank M (2004) Use of pteridine nucleoside analogs as hybridization probes. Nucleic Acids Res 32:e62