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通过分子识别控制 DNA 修饰金纳米粒子的可逆聚集。

Reversible aggregation of DNA-decorated gold nanoparticles controlled by molecular recognition.

机构信息

Institute of Food, Nutrition and Health, Department of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.

出版信息

Langmuir. 2013 Aug 27;29(34):10824-30. doi: 10.1021/la401211u. Epub 2013 Aug 19.

Abstract

The programmable assembly of functional nanomaterials has been extensively addressed; however, their selective reversible assembly in response to an external stimulus has been more difficult to realize. The specificity and programmable interactions of DNA have been exploited for the rational self-assembly of DNA-conjugated nanoparticles, and here we demonstrate the sequence-controlled disaggregation of DNA-modified gold nanoparticles simply by employing two complementary oligonucleotides. Target oligonucleotides with perfectly matching sequence enabled dissociation of aggregated nanoparticles, whereas oligonucleotides differing by one nucleotide did not cause disassembly of the aggregated nanoparticles. Physical aspects of this process were characterized by UV-vis absorption, light scattering, and transmission electron microscopy. This strategy for programmed disassembly of gold nanoparticles in response to biological stimuli demonstrates a fundamentally important concept anticipated to be useful for diverse applications involving molecular recognition.

摘要

功能纳米材料的可编程组装已经得到了广泛的研究;然而,它们对外界刺激的选择性可逆组装更难实现。DNA 的特异性和可编程相互作用已被用于 DNA 修饰纳米粒子的合理自组装,在这里,我们通过使用两个互补的寡核苷酸来展示 DNA 修饰的金纳米粒子的序列控制解聚。具有完全匹配序列的靶寡核苷酸能够使聚集的纳米粒子解离,而仅相差一个核苷酸的寡核苷酸则不会导致聚集的纳米粒子解体。该过程的物理方面通过紫外可见吸收、光散射和透射电子显微镜进行了表征。这种针对生物刺激的金纳米粒子的程序化拆卸策略展示了一个重要的基本概念,预期对涉及分子识别的各种应用有用。

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