Prado-Gotor R, Grueso E
Department of Physical Chemistry, Faculty of Chemistry, University of Sevilla, C/Profesor García González S/N, 41012 Sevilla, Spain.
ScientificWorldJournal. 2014 Jan 22;2014:143645. doi: 10.1155/2014/143645. eCollection 2014.
The binding of gold nanoparticles capped with N-(2-mercaptopropionyl)glycine (Au@tiopronin) with double-stranded DNA has been investigated and quantified in terms of free energies by using two different approaches. The first approach follows the DNA conformational changes induced by gold nanoparticles using the CD technique. The second methodology consists in the use of pyrene-1-carboxaldehyde as a fluorescent probe. This second procedure implies the determination of the "true" free energy of binding of the probe with DNA, after corrections through solubility measurements. Working at different salt concentrations, the nonelectrostatic and electrostatic components of the binding free energy have been separated. The results obtained revealed that the binding is of nonelectrostatic character, fundamentally. The procedure used in this work could be extended to quantify the binding affinity of other AuNPs/DNA systems.
研究了用N-(2-巯基丙酰基)甘氨酸包覆的金纳米颗粒(Au@tiopronin)与双链DNA的结合情况,并通过两种不同方法从自由能角度进行了量化。第一种方法利用圆二色(CD)技术追踪金纳米颗粒诱导的DNA构象变化。第二种方法是使用芘-1-甲醛作为荧光探针。第二个步骤意味着在通过溶解度测量进行校正之后,确定探针与DNA结合的“真实”自由能。在不同盐浓度下开展工作,已将结合自由能的非静电和静电成分区分开来。所得结果表明,该结合基本上具有非静电性质。本工作中使用的方法可扩展用于量化其他金纳米颗粒/DNA系统的结合亲和力。