Synthesis and characterization of covalent adducts derived from the binding of benzo[a]pyrene diol epoxide to a -ggg- sequence in a deoxyoligonucleotide

Bing Mao, Jing Xu, Bin Li, Leonid A. Margulis, Sergey Smirnov, Nai Qi Ya, Scott H. Courtney, Nicholas E. Geacintov

Research output: Contribution to journalArticlepeer-review

Abstract

Direct synthesis and purification procedures are described for the preparation of adducts derived from the covalent binding of 7R,8S-dihydroxy-9S,10R-epoxy-7,8,9,10-tetrahydro-benzo[a]pyrene [(+)-ante-BPDE or (+)-BPDE 2] to each of the three guanine residues (trans-N2 lesions) in the oligodeoxyribonucleotide d(CTATG1G2G3TATC) The positions of the modified Gs are defined by Maxam-Gilbert sequencing techniques. Six different oligonucleotides with one or two precisely positioned (+)-anti-BPDE residues are identified. The absorbance, circular dichroism and fluorescence characteristics are changed upon formation of duplexes with the complementary strands d(GATACCCATAG). In the doubly-modified oligonucleotides, a broad, excimer-like long wavelength fluorescence emission band is observed with a maximum near 455 nm only if the two (+)-anti-BPDE-modified Gs are adjacent to one another. The covalently attached (+)-anti-BPDE residues decrease the thermodynamic stabilities of the duplexes; their melting points are markedly dependent on the position of the lesions, being highest with the (+)-anti-BPDE residue at G1 (Tm=40°C, only 2°C lower than in the case of the unmodified oligonucleotide) and lowest when it is situated at G3 (Tm=29°C). The implications of these and other physical characteristics are discussed. The facile synthesis of these or similar site-specific and stereochemically defined (+)-trans-anti-BPDE-N2-dG lesions in runs of contiguous guanines in oligodeoxyribonucleotides of specified base sequence should be useful for the design of site-directed mutagenesis studies in vitro and in vivo.

Original languageEnglish (US)
Pages (from-to)357-365
Number of pages9
JournalCarcinogenesis
Volume16
Issue number2
DOIs
StatePublished - Feb 1995

ASJC Scopus subject areas

  • Cancer Research

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