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DNA 功能化的 2nm 金纳米粒子在纳米通道阵列中的特性和电化学响应。

Characterization and electrochemical response of DNA functionalized 2nm gold nanoparticles confined in a nanochannel array.

机构信息

INQUIMAE (CONICET), Departamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellón 2, C1428EHA Buenos Aires, Argentina.

Universidad Nacional de Gral. Sarmiento, J. M. Gutierrez 1150, B1613GSX Los Polvorines, Prov. de Bs. As., Argentina.

出版信息

Bioelectrochemistry. 2018 Jun;121:169-175. doi: 10.1016/j.bioelechem.2018.02.002. Epub 2018 Feb 9.

Abstract

Polyvalent gold nanoparticle oligonucleotide conjugates are subject of intense research. Even though 2nm diameter AuNPs have been previously modified with DNA, little is known about their structure and electrochemical behavior. In this work, we examine the influence of different surface modification strategies on the interplay between the meso-organization and the molecular recognition properties of a 27-mer DNA strand. This DNA strand is functionalized with different sulfur-containing moieties and immobilized on 2nm gold nanoparticles confined on a nanoporous alumina, working the whole system as an electrode array. Surface coverages were determined by EXAFS and the performance as recognition elements for impedance-based sensors is evaluated. Our results prove that low DNA coverages on the confined nanoparticles prompt to a more sensitive response, showing the relevance in avoiding the DNA strand overcrowding. The system was able to determine a concentration as low as 100pM of the complementary strand, thus introducing the foundations for the construction of label-free genosensors at the nanometer scale.

摘要

多价金纳米粒子寡核苷酸缀合物是目前研究的热点。尽管之前已经对 2nm 直径的 AuNPs 进行了 DNA 修饰,但对于它们的结构和电化学行为却知之甚少。在这项工作中,我们研究了不同表面修饰策略对 27 个碱基 DNA 链的介观组织与分子识别特性相互作用的影响。该 DNA 链通过不同的含硫部分进行功能化,并固定在受限的纳米金颗粒上,该纳米金颗粒被限制在纳米多孔氧化铝中,整个系统作为一个电极阵列。通过 EXAFS 确定了表面覆盖率,并评估了基于阻抗的传感器作为识别元件的性能。我们的结果证明,受限纳米颗粒上的低 DNA 覆盖率可促使更灵敏的响应,表明避免 DNA 链拥挤的重要性。该系统能够检测到低至 100pM 的互补链,从而为在纳米尺度上构建无标记基因传感器奠定了基础。

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