Interaction of Cu-dipeptide complexes with Calf Thymus DNA and antiproliferative activity of [Cu(ala-phe)] in osteosarcoma-derived cells

In this work the study of Calf Thymus DNA interaction with several Cu(l-dipeptide) complexes was reported. The binding stoichiometry (Cu(mmol)/DNAmol base) was determined and in an attempt to clarify the binding mode, EPR and CD experiments were performed. All the studied complexes interacted with DNA, in a more selective way than [Cu(H2O)6]2+, being the [Cu(ala-phe)] the complex with the highest interaction. The EPR experiments suggested that the monomeric species formed in solution were coordinated through a nitrogen atom of the DNA bases (inner-sphere binding) and the CD studies showed structural changes upon the DNA–complex interaction. Besides, the ratio Cu(mmol)/DNAmol base obtained by the binding stoichiometry experiments was close to that found by EPR and CD determinations. The effect on cell proliferation determined by the crystal violet bioassay on UMR106 rat osteosarcoma-derived cells showed that the [Cu(ala-phe)] complex exerted an antiproliferative action against this tumor line.

The study of the Calf Thymus DNA interaction with several Cu(l-dipeptide) complexes is presented. The binding stoichiometry (amount of copper bound to the DNA) was quantified and in an attempt to clarify the mode of binding, EPR and CD experiments were performed. The effect on cell proliferation determined on rat asteosarcoma-derived cells was stuided.Figure optionsDownload as PowerPoint slide