Biver Tarita, Secco Fernando, Tinè Maria Rosaria, Venturini Marcella
Dipartimento di Chimica e Chimica Industriale, Università di Pisa, Via Risorgimento 35, 56126 Pisa, Italy.
Arch Biochem Biophys. 2003 Oct 1;418(1):63-70. doi: 10.1016/s0003-9861(03)00384-9.
The interaction of the cis-platinum derivative of proflavine [PtCl(tmen)(2)][HNC(13)H(7)(NHCH(2)CH(2))(2)] (PRPt) with CT-DNA is investigated by spectrophotometry and T-jump relaxation in 0.11M NaCl, pH 7.0, and 25 degrees C. The DNA-proflavine (PR) system is investigated under the same conditions. Static measurements indicate that base-dye interactions prevail and their analysis reveals that the site size for PRPt (n=2.6) is twice that found for PR (n=1.3). One relaxation effect is observed for the DNA/PR system and two effects for the DNA/PRPt system, the faster of them being similar to that of DNA/PR. The kinetics of the process are discussed in terms of the three-step sequence D+S <= => DS(I) <= => DS(II) <= => DS(III), where PR and the aromatic residues of PRPt intercalate into DNA by the same mechanism. The third step represents the penetration of platinum residues between base-pairs and is associated to remarkable enthalpy and entropy changes. Further mechanistic details are discussed.
通过分光光度法和T跳跃弛豫技术,在0.11M NaCl、pH 7.0和25℃条件下研究了原黄素的顺铂衍生物[PtCl(tmen)(2)][HNC(13)H(7)(NHCH(2)CH(2))(2)](PRPt)与CT-DNA的相互作用。在相同条件下研究了DNA-原黄素(PR)体系。静态测量表明碱基-染料相互作用占主导,分析显示PRPt的结合位点大小(n = 2.6)是PR的两倍(n = 1.3)。在DNA/PR体系中观察到一种弛豫效应,在DNA/PRPt体系中观察到两种效应,其中较快的效应与DNA/PR的相似。根据三步序列D + S <= => DS(I) <= => DS(II) <= => DS(III)讨论了该过程的动力学,其中PR和PRPt的芳香族残基通过相同机制插入DNA。第三步代表铂残基在碱基对之间的插入,与显著的焓变和熵变相关。进一步讨论了详细的作用机制。