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一种通过局部表面等离子体共振技术监测的过氧化物酶模拟 DNA 酶用于金纳米粒子上银沉积的新策略。

A New Strategy for Silver Deposition on Au Nanoparticles with the Use of Peroxidase-Mimicking DNAzyme Monitored via a Localized Surface Plasmon Resonance Technique.

机构信息

Laboratory of Bioanalytical Chemistry, Faculty of Chemistry, Adam Mickiewicz University, Umultowska 89b, 61-614 Poznan, Poland.

Department of Nano Biophotonics, Leibniz Institute of Photonic Technology (IPHT), 07745 Jena, Germany.

出版信息

Sensors (Basel). 2017 Apr 13;17(4):849. doi: 10.3390/s17040849.

Abstract

Peroxidase-mimicking DNAzyme was applied as a catalyst of silver deposition on gold nanoparticles. This DNAzyme is formed when hemin binds to the G-quadruplex-forming DNA sequence. Such a system is able to catalyze a redox reaction with a one- or two-electron transfer. The process of silver deposition was monitored via a localized surface plasmon resonance technique (LSPR), which allows one to record scattering spectrum of a single nanoparticle. Our study showed that DNAzyme is able to catalyze silver deposition. The AFM experiments proved that DNAzyme induced the deposition of silver shells of approximately 20 nm thickness on Au nanoparticles (AuNPs). Such an effect is not observed when hemin is absent in the system. However, we noticed non-specific binding of hemin to the capture oligonucleotides on a gold NP probe that also induced some silver deposition, even though the capture probe was unable to form G-quadruplex. Analysis of SEM images indicated that the surface morphology of the silver layer deposited by DNAzyme is different from that obtained for hemin alone. The proposed strategy of silver layer synthesis on gold nanoparticles catalyzed by DNAzyme is an innovative approach and can be applied in bioanalysis (LSPR, electrochemistry) as well as in material sciences.

摘要

过氧化物酶模拟 DNA 酶被用作金纳米粒子上银沉积的催化剂。当血红素结合到形成 G-四链体的 DNA 序列时,就会形成这种 DNA 酶。该系统能够催化具有单电子或双电子转移的氧化还原反应。银沉积的过程通过局域表面等离子体共振技术(LSPR)进行监测,该技术允许记录单个纳米粒子的散射光谱。我们的研究表明,DNA 酶能够催化银的沉积。AFM 实验证明,DNA 酶诱导约 20nm 厚的银壳在 Au 纳米粒子(AuNPs)上沉积。当系统中不存在血红素时,不会观察到这种效应。然而,我们注意到血红素与金纳米粒子探针上的捕获寡核苷酸发生非特异性结合,这也诱导了一些银沉积,尽管捕获探针无法形成 G-四链体。SEM 图像分析表明,由 DNA 酶催化的金纳米粒子上银层的沉积表面形貌与血红素单独存在时的形貌不同。该策略通过 DNA 酶催化在金纳米粒子上合成银层是一种创新方法,可应用于生物分析(LSPR、电化学)以及材料科学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b5f/5424726/32a058cc38a2/sensors-17-00849-sch001.jpg

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