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Title: Proton NMR study of the effects of the alkylated base and sugar-phosphate backbone on the structure and conformation of DNA

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5095355

The modified base and/or sugar-phosphate are of prime importance for studying mutagenesis and carcinogenesis. A decadeoxynucleotide of defined sequence (structure I) was used as a model to introduce (alkylated) modifications and study their effects on the structure and conformation of the model compound by proton NMR spectroscopy. Three alkylated decadeoxynucleotides have been studied so far. Two of them are optical isomers (R and S forms) of the chiral ethylphosphotriester placed between G(5) and A(6) of (I). The third oligomer contains an 06-methyl guanine base at the G(5) position of (I). The stability and dynamic behavior of these decamers involved in a double-stranded helix (base-paired with another chemically synthesized unmodified decamer with proper sequence) are different from that of the normal oligomer with the same sequence. Additional investigation of the self-association of two decamers with the ethylphosphotriester modification also forms G-A base pairs, but with lower melting temperature, as the nonalkylated oligomer (I). Thus, the study of these modified helices may yield information on the transcriptional mechanism and rate of DNA. The possible structure of these helices will be discussed.

Research Organization:
Johns Hopkins Univ., Baltimore, MD
OSTI ID:
5095355
Report Number(s):
CONF-8606151-; TRN: 86-034875
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 45:6; Conference: 76. annual meeting of the Federation of American Society for Experimental Biology, Washington, DC, USA, 8 Jun 1986
Country of Publication:
United States
Language:
English