Department of Physical Chemistry, Faculty of Chemistry, University of Sevilla, C/Profesor García González s/n, 41012 Sevilla, Spain.
Phys Chem Chem Phys. 2011 Jan 28;13(4):1479-89. doi: 10.1039/c0cp00901f. Epub 2010 Dec 6.
A kinetic study of the interaction of gold nanoparticles capped with N-(2-mercaptopropionyl)glycine with double stranded DNA was carried out in water and in salt (NaCl) solutions. The kinetic curves are biexponential and reveal the presence of three kinetic steps. The dependence of the reciprocal fast and slow relaxation time, on the DNA concentration, is a curve and tends to a plateau at high DNA concentrations. The simplest mechanism consistent with the kinetic results involves a simple three-step series mechanism reaction scheme. The first step corresponds to a very fast step that is related to a diffusion controlled formation of an external precursor complex (DNA, AuNPs); the second step involves the formation of a (DNA/AuNPs)(I) complex, as a result of the binding affinity between hydrophilic groups of the tiopronin and the DNA grooves. Finally, the third step has been interpreted as a consequence of a conformational change of the (DNA/AuNPs)(I) complex formed in the second step, to a more compacted form (DNA/AuNPs)(II). The values of the rate constants of each step decrease as NaCl concentration increases. The results have been discussed in terms of solvation of the species and changes in the viscosity of the solution.
采用振动样品磁强计研究了在水和盐(NaCl)溶液中,巯基乙酸(MPA)保护的金纳米粒子与双链 DNA 的相互作用的动力学。动力学曲线为双指数型,揭示了三个动力学步骤的存在。快速和慢速松弛时间的倒数与 DNA 浓度的依赖性是一条曲线,并在高 DNA 浓度下趋于平台。与动力学结果一致的最简单机制涉及一个简单的三步串联反应方案。第一步对应于一个非常快速的步骤,与扩散控制的外部前体复合物(DNA、AuNPs)的形成有关;第二步涉及(DNA/AuNPs)(I)复合物的形成,这是由于亲水基团的巯基乙酸与 DNA 沟槽之间的结合亲和力所致。最后,第三步被解释为第二步形成的(DNA/AuNPs)(I)复合物的构象变化的结果,形成更紧凑的形式(DNA/AuNPs)(II)。随着 NaCl 浓度的增加,每个步骤的速率常数值减小。结果根据物种的溶剂化和溶液粘度的变化进行了讨论。