Key Laboratory of Ion Beam Bioengineering, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031, Anhui, PR China.
Langmuir. 2011 Nov 15;27(22):13629-34. doi: 10.1021/la203632c. Epub 2011 Oct 14.
Gold nanoparticles conjugated with DNA represent an attractive and alternative platform for broad applications in biosensors, medical diagnostic, and biological analysis. However, current methods to conjugate DNA to gold nanoparticles are time-consuming. In this study, we report a novel approach to rapidly conjugate DNA to gold nanoparticles (AuNPs) to form functional DNA/AuNPs in 2-3 h using Tween 80 as protective agent. With a fluorescence-based technique, we determine that the DNA density on the surface of AuNPs achieves about ∼60 strands per particles, which is comparable to the loading density in the current methods. Moreover, the DNA/AuNPs synthesized by our approach exhibit an excellent stability as a function of temperature, pH, and freeze-thaw cycle, and the functionality of DNA/AuNPs conjugates is also verified. The work presented here has important implications to develop the fast and reproducible synthesis of stable DNA-functionalized gold nanoparticles.
金纳米粒子与 DNA 的结合代表了一种有吸引力的替代平台,可广泛应用于生物传感器、医学诊断和生物分析。然而,目前将 DNA 与金纳米粒子结合的方法耗时较长。在这项研究中,我们报告了一种新的方法,可以在 2-3 小时内使用吐温 80 作为保护剂将 DNA 快速结合到金纳米粒子(AuNPs)上,形成功能性的 DNA/AuNPs。我们使用基于荧光的技术确定,AuNPs 表面上的 DNA 密度达到约每颗粒约 60 个链,与当前方法中的加载密度相当。此外,我们方法合成的 DNA/AuNPs 在温度、pH 值和冻融循环下表现出优异的稳定性,并且 DNA/AuNPs 缀合物的功能也得到了验证。本工作对于开发快速且可重复的稳定 DNA 功能化金纳米粒子的合成具有重要意义。