DNA interaction studies of selected polyamine conjugates

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Abstract

The interaction of polyamine conjugates with DNA double helix has been studied. Binding properties were examined by ethidium bromide (EtBr) displacement and DNA unwinding/topoisomerase I/II (Topo I/II) activity assays, as well as dsDNA thermal stability studies and circular dichroism spectroscopy. Genotoxicity of the compounds was estimated by a comet assay. It has been shown that only compound 2a can interact with dsDNA via an intercalative binding mode as it displaced EtBr from the dsDNA-dye complex, with Kapp = 4.26 × 106 M-1; caused an increase in melting temperature; changed the circular dichroism spectrum of dsDNA; converted relaxed plasmid DNA into a supercoiled molecule in the presence of Topo I and reduced the amount of short oligonucleotide fragments in the comet tail. Furthermore, preliminary theoretical study has shown that interaction of the discussed compounds with dsDNA depends on molecule linker length and charge distribution over terminal aromatic chromophores.

Figures

  • Table 1. C50 and Kapp values for tested compounds.
  • Table 2. Influence of examined compounds on the thermal stability of dsDNA.
  • Figure 6. DNA damage in leukemia cells induced by 1a (A), 1b (B), 2a (C) and 2b (D) (60 min, 37 °C) at concentrations of 5, 10 and 15 µM with and without prior H2O2 incubation (10 min, 4 °C) at a concentration of 15 µM with respect to the appropriate control (−H2O2/+H2O2). The values were measured as the average percentage of DNA in the comet tail ± SEM using alkaline version of comet assay.
  • Figure 6. DNA damage in leukemia cells induced by 1a (A), 1b (B), 2a (C) and 2b (D) (60 min, 37 °C) at concentrations of 5, 10 and 15 µM with and without prior H2O2 incubation (10 min, 4 °C) at a concentration of 15 µM with respect to the appropriate control (−H2O2/+H2O2). The values were measured as the average percentage of DNA in the comet tail ± SEM using alkaline version of comet assay.
  • Figure 7. The circular dichroism spectra of pure ct-DNA 100 µM (solid) and ct-DNA incubated with 2a at concentration of 10 µM (dots).
  • Figure 8. The CD spectra of pure ds-oligonucleotide 2.5 µM (solid), ds-oligonucleotide with 2a at a concentration of 2.5 µM added before hybridization (ON1—dots) and ds-oligonucleotide with 2a at a concentration of 2.5 µM added after hybridization (ON2—dashes).

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APA

Szumilak, M., Merecz, A., Strek, M., Stanczak, A., Inglot, T. W., & Karwowski, B. T. (2016). DNA interaction studies of selected polyamine conjugates. International Journal of Molecular Sciences, 17(9). https://doi.org/10.3390/ijms17091560

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