A wide variety of compounds bind to DNA by intercalation. While the average affinity of these intercalators for DNA is similar, not all intercalators are effective in the treatment of cancer. The molecular basis for this behavior is sought. What makes an intercalating compound an effective cancer drug? My hypothesis is that the intercalators effective in cancer chemotherapy recognize some feature of the DNA in proliferating cells that the less effective intercalators do not, either a particular DNA conformation or sequence. Previous work on the cancer drug daunomycin indicated that one possible distinguishing trait is the ability to discriminate """"""""free"""""""" DNA from DNA structured into nucleosomes. The proposed research will explore the nucleosome as a drug receptor in three ways. First, the binding of a wide variety of intercalators to """"""""free"""""""" DNA and to nucleosomes will be studied, to see if the clinically effective compounds show discriminating behavior analogous to daunomycin. Second, stopped-flow and temperature-jump studies will be used to develop plausible reaction mechanisms for the binding of ethidium and daunomycin to nucleosomes. Finally, photochemical crosslinking experiments will be performed to localize drug binding sites within the nucleosomal DNA, in order to establish if all possible intercalation sites are freely accessible. In a separate aspect of the proposed research, the sequence specificity of anthracycline antibiotics widely used in cancer chemotherapy, will be explored using photochemical crosslinking, modern """"""""footprinting"""""""" techniques, and affinity chromatography. Finally, the influence of intercalators on the B to Z transition will be studied, to define the role of intercalators as allosteric effectors of DNA conformational changes. The information obtained from these studies will enhances our fundamental understanding of an important class of ligand-DNA interactions, and should provide a foundation for the rational design of new chemotherapeutic compounds of greater specificity and potency.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA035635-03
Application #
3173228
Study Section
Biophysics and Biophysical Chemistry A Study Section (BBCA)
Project Start
1984-03-01
Project End
1988-01-31
Budget Start
1986-03-01
Budget End
1988-01-31
Support Year
3
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Mississippi Medical Center
Department
Type
Schools of Medicine
DUNS #
928824473
City
Jackson
State
MS
Country
United States
Zip Code
39216
Del Villar-Guerra, Rafael; Trent, John O; Chaires, Jonathan B (2018) G-Quadruplex Secondary Structure Obtained from Circular Dichroism Spectroscopy. Angew Chem Int Ed Engl 57:7171-7175
Del Villar-Guerra, Rafael; Gray, Robert D; Chaires, Jonathan B (2017) Characterization of Quadruplex DNA Structure by Circular Dichroism. Curr Protoc Nucleic Acid Chem 68:17.8.1-17.8.16
Bon?ina, Matjaž; Vesnaver, Gorazd; Chaires, Jonathan Brad et al. (2016) Unraveling the Thermodynamics of the Folding and Interconversion of Human Telomere G-Quadruplexes. Angew Chem Int Ed Engl 55:10340-4
Chaires, Jonathan B; Dean, William L; Le, Huy T et al. (2015) Hydrodynamic Models of G-Quadruplex Structures. Methods Enzymol 562:287-304
Chaires, Jonathan B (2015) A small molecule--DNA binding landscape. Biopolymers 103:473-9
Zhao, Huaying; Ghirlando, Rodolfo; Alfonso, Carlos et al. (2015) A multilaboratory comparison of calibration accuracy and the performance of external references in analytical ultracentrifugation. PLoS One 10:e0126420
Le, Huy T; Dean, William L; Buscaglia, Robert et al. (2014) An investigation of G-quadruplex structural polymorphism in the human telomere using a combined approach of hydrodynamic bead modeling and molecular dynamics simulation. J Phys Chem B 118:5390-405
Gray, Robert D; Trent, John O; Chaires, Jonathan B (2014) Folding and unfolding pathways of the human telomeric G-quadruplex. J Mol Biol 426:1629-50
Chaires, Jonathan B; Trent, John O; Gray, Robert D et al. (2014) An improved model for the hTERT promoter quadruplex. PLoS One 9:e115580
Buscaglia, Robert; Miller, M Clarke; Dean, William L et al. (2013) Polyethylene glycol binding alters human telomere G-quadruplex structure by conformational selection. Nucleic Acids Res 41:7934-46

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