Add time:08/04/2019         Source:sciencedirect.com

The interaction of the anticancer antibiotic altromycin B and its isostructrural Pt(II) and Pd(II) metal complexes with native calf thymus (CT) DNA was studied using UV–thermal denaturation experiments, circular dichroism spectroscopy and temperature controlled spectrophotometric titrations. Altromycin B stabilizes the double helix by raising the Tm, mainly by intercalation of its chromophore between the base pairs and interacting electrostatically via its sugar moieties with the edges of the DNA helix. Moreover, altromycin B induces a B→A structural transition of CT DNA. The effect on DNA stability and conformation depends on the metal ion. Pt(II) and Pd(II) complexes induce the B→A structural transition and stabilize the double helix similarly but they present lower final hyperchromicity due to premelting effects which were caused by intra- and interstrand crosslinking. Thus, a synergic effect of the metal ions to altromycin B–CT DNA interaction is observed in both cases. Altromycin B interacts with 5′-GMP, 5′-AMP and 5′-CMP by electrophilic attack of the opened epoxide ring to the N(7)G, N(1)/N(7)A and N(3)C. Thus, covalent binding between these nucleotides and altromycin B takes place and explain the multiple binding mode suggested by the studies of the interaction of altromycin B and its complexes with DNA. The [Pd(II)–altroB] complex dissociates in the presence of the nucleotides, and various species of Pd(II)–nucleotide complexes, especially with 5′-GMP, are formed. The [Pt(II)–altroB] complex dissociates too, but only one or two species of Pt(II)–nucleotide complexes are formed, and in the case of 5′-AMP interaction the formation of a tertiary altroB–Pt(II)–5′AMP complex is proposed. 5′-TMP reacts very weakly in comparison with the other three nucleotides. These interactions were followed by 1H-NMR.

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