1998
DOI: 10.1103/physreve.58.7754
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Observation of two-mode binding to DNA by bipyridyl-(ethylenediamine)platinum(II): Isothermal titrational calorimetry and midinfrared absorption studies

Abstract: The binding of bipyridyl-͑ethylenediamine͒platinum͑II͒ to calf-thymus DNA has been studied in solution via isothermal titration calorimetry and in unoriented films via midinfrared spectroscopy. The calorimetric data reveal that the ligand binds to DNA at two different sites with the first binding site being filled by about one ligand for every five base pairs. The binding is entropically driven: ϩ25 cal/mol K for the first site and ϩ22 cal/mol K for the second site. Midinfrared absorption data (400-1800 cm Ϫ1 … Show more

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Cited by 5 publications
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“…18 These generally are planar heterocyclic aromatic molecules, such as ethidium and daunomycin, 19 which are able to insert themselves between neighbouring DNA base pairs causing distortion of the sugarphosphate backbone at the intercalation site. 20 The intercalation process requires both electrostatic interactions of the positive charges of the compounds with the negatively charged phosphate oxygens of DNA and stacking between the aromatic rings of the intercalator and the DNA nucleobases. In the presence of intercalation processes in vivo inhibition of the nucleic acid synthesis is observed and the intercalating compounds show mutagenic, antibiotic, antibacterial and antitumor activity.…”
Section: Introductionmentioning
confidence: 99%
“…18 These generally are planar heterocyclic aromatic molecules, such as ethidium and daunomycin, 19 which are able to insert themselves between neighbouring DNA base pairs causing distortion of the sugarphosphate backbone at the intercalation site. 20 The intercalation process requires both electrostatic interactions of the positive charges of the compounds with the negatively charged phosphate oxygens of DNA and stacking between the aromatic rings of the intercalator and the DNA nucleobases. In the presence of intercalation processes in vivo inhibition of the nucleic acid synthesis is observed and the intercalating compounds show mutagenic, antibiotic, antibacterial and antitumor activity.…”
Section: Introductionmentioning
confidence: 99%