Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Proton NMR investigation of tris(phenanthroline)ruthenium(II) enantiomers bound to synthetic deoxyribonucleic acid hexamers

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5022479
The binding of tris(phenanthroline)ruthenium(II), Ru(phen)/sub 3//sup 2 +/, to DNA is both enantioselective, and DNA sequence and conformation dependent. There is a chiral preference for ..delta..-Ru(phen)/sub 3//sup 2 +/ for the intercalative mode of binding and a surface bound mode shows a weak preference for Lambda-Ru(phen)/sub 3//sup 2 +/. Proton NMR techniques are being used to characterize the solution structure of ..delta..-Ru(phen)/sub 3//sup 2 +/ and Lambda-Ru(phen)/sub 3//sup 2 +/ bound to specific DNA sequences. The Proton NMR resonances of both enantiomers are shifted upfield when bound to the hexamers d(pApT)/sub 3/ and d(pCpG)/sub 3/, and the spectra of the ..delta..- and Lambda-isomers, superimposed in free solution, may be resolved in the presence of DNA. Furthermore, sequence dependent shifts are evident for both enantiomers. Two-dimensional NOESY spectroscopy is being used to elucidate the bound conformation of the DNA-Ru(phen)/sub 3//sup 2 +/ complexes.
Research Organization:
Columbia Univ., New York, NY
OSTI ID:
5022479
Report Number(s):
CONF-8606151-
Conference Information:
Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Journal Volume: 45:6
Country of Publication:
United States
Language:
English