DNA-conjugated metal nanoparticle for bioanalytics, nanophotonics, and nanoelectronics

W. Fritzsche, A. Csáki, R. Möller, A. Steinbrück, G. Festag, A. Wolff, T. Schüler
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引用次数: 0

Abstract

Metal (especially gold) nanoparticles exhibit unique electronic, optical, and catalytic properties. In order to utilize these properties, an integration of the particles into technical setups such as a chip surface is helpful. We develop techniques to use (bio) molecular tools in order to address and control the positioning of particles on microstructured chips. These techniques are utilized for novel DNA detection schemes using optical or electrical principles. Plasmonic properties of the particles and the combination of nano-apertures with particles are promising fields for further bioanalytical developments. On the other hand, methods for defined positioning of single molecules or molecular constructs in parallel approaches are under development, in order to provide needed defined nanostructures for applications in nanoelectronics. Connecting DNA with nanoparticles, metallization of DNA or positioning of individual DNA-structures over microstructured electrode gap including subsequent metal particle binding are important steps in this direction. The utilization of (bio) molecular tools and principles based on highly specific binding and self-assembly represent a promising development in order to realize novel nanoparticle-based devices for bioanalytics, nano-optics and - electronics.
用于生物分析、纳米光子学和纳米电子学的dna共轭金属纳米粒子
金属(尤其是金)纳米颗粒具有独特的电子、光学和催化性能。为了利用这些特性,将颗粒集成到技术设置(如芯片表面)中是有帮助的。我们开发了使用(生物)分子工具的技术,以解决和控制微结构芯片上颗粒的定位。这些技术被用于使用光学或电学原理的新型DNA检测方案。粒子的等离子体特性以及纳米孔与粒子的结合是生物分析的发展方向。另一方面,为了提供纳米电子学应用所需的定义纳米结构,在平行方法中定义单分子或分子结构定位的方法正在开发中。将DNA与纳米颗粒连接,DNA的金属化或将单个DNA结构定位在微结构电极间隙上,包括随后的金属颗粒结合,是该方向的重要步骤。利用基于高度特异性结合和自组装的(生物)分子工具和原理,实现基于纳米粒子的新型生物分析、纳米光学和电子器件是一个有前途的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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