Interaction of the Alternating Double Stranded Copolymer poly(dA-dT)·poly(dA-dT) with NiCl2 and CdCl2: Solution Behavior
- Autori: Airoldi, M.; Gennaro, G.; Giomini, M.; GIULIANI RICCI, A.; Giustini, M.
- Anno di pubblicazione: 2007
- Tipologia: Articolo in rivista (Articolo in rivista)
- Parole Chiave: Model polynucleotides; Thermal denaturation; Nickel (II) and Cadmium (II) ions; Circular Dichroism; UV-spectroscopy
- OA Link: http://hdl.handle.net/10447/11496
The thermal denaturation of the synthetic high molecular weight double stranded polynucleotide poly(dA-dT)·poly(dA-dT) has been studied in aqueous buffered solution (Tris 1.0mM; pH 7.8±0.2) in the presence of increasing concentrations of either Ni2+ (borderline cation) or Cd2+ (soft cation) at four different constant ionic strength values (NaCl), making use of UV and circular dichroism (CD) spectroscopies. The experimental results show that the B-type double helix of the polymer is stabilized against thermal denaturation in the presence of both cations at low concentrations, relative to the systems where only NaCl is present, in the same conditions of ionic strength and pH. The effect is more pronounced for Ni2+ than for Cd2+. At higher concentrations, both cations start to destabilize the double helix, with Cd cations inducing larger variations of Tm. In many cases, when denaturation starts, interstrand cross-linking occurs with formation of aggregates that precipitate.