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基于配位作用的等离子体银纳米粒子上未经修饰寡核苷酸的可编程组装。

Coordination-mediated programmable assembly of unmodified oligonucleotides on plasmonic silver nanoparticles.

出版信息

ACS Appl Mater Interfaces. 2015 May 27;7(20):11047-52. doi: 10.1021/acsami.5b03066. Epub 2015 May 12.

Abstract

DNA-decorated metal nanoparticles have found numerous applications, most of which rely on thiolated DNA (SH-DNA)-modified gold nanoparticles (AuNPs). Whereas silver nanoparticles (AgNPs) are known to have stronger plasmonic properties than AuNPs, modification of AgNPs with SH-DNA is technically challenging, partially due to the instability of Ag-S bonding. Here we demonstrate a facile approach to self-assemble unmodified DNA on AgNPs by exploiting intrinsic silver-cytosine (Ag-C) coordination. The strong Ag-C coordination allows for the ready formation of DNA-AgNP conjugates, which show favorable stability under conditions of high ionic strength and high temperature. These nanoconjugates possess much higher efficient molecular recognition capability and faster hybridization kinetics than thiolated DNA-modified AgNPs. More importantly, we could programmably tune the DNA density on AgNPs with the regulation of silver-cytosine coordination numbers, which in turn modulated their hybridizability. We further demonstrated that these DNA-AgNP conjugates could serve as excellent building blocks for assembling silver and hybrid silver-gold nanostructures with superior plasmonic properties.

摘要

DNA 修饰的金属纳米粒子有许多应用,其中大多数依赖于巯基化 DNA(SH-DNA)修饰的金纳米粒子(AuNPs)。虽然已知银纳米粒子(AgNPs)具有比 AuNPs 更强的等离子体特性,但用 SH-DNA 修饰 AgNPs 在技术上具有挑战性,部分原因是 Ag-S 键的不稳定性。在这里,我们展示了一种通过利用内在的银-胞嘧啶(Ag-C)配位来在 AgNPs 上自组装未修饰 DNA 的简便方法。强的 Ag-C 配位允许 DNA-AgNP 缀合物的快速形成,在高离子强度和高温条件下具有良好的稳定性。与巯基化 DNA 修饰的 AgNPs 相比,这些纳米缀合物具有更高的有效分子识别能力和更快的杂交动力学。更重要的是,我们可以通过调节银-胞嘧啶配位数来对 AgNPs 上的 DNA 密度进行编程,从而调节它们的杂交能力。我们进一步证明,这些 DNA-AgNP 缀合物可用作组装具有优异等离子体性能的银和混合银金纳米结构的优异构建块。

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