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量子点功能化的多孔氧化锌纳米片作为用于DNA检测的可见光诱导光电化学平台。

Quantum dot-functionalized porous ZnO nanosheets as a visible light induced photoelectrochemical platform for DNA detection.

作者信息

Wang Wenjing, Hao Qing, Wang Wei, Bao Lei, Lei Jianping, Wang Quanbo, Ju Huangxian

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, P.R. China.

出版信息

Nanoscale. 2014 Mar 7;6(5):2710-7. doi: 10.1039/c3nr04777f. Epub 2014 Jan 24.

Abstract

This work reports the synthesis of novel CdTe quantum dot (QD)-functionalized porous ZnO nanosheets via a covalent binding method with (3-aminopropyl)triethoxysilane as a linker. The functional nanosheets showed an excellent visible-light absorbency and much higher photoelectrochemical activity than both CdTe QDs and ZnO nanosheets due to the porous structure and appropriate band alignment between the CdTe QDs and ZnO nanosheets. Using hydrogen peroxide as an electron acceptor the nanosheet-modified electrode showed a sensitive photocurrent response. This speciality led to a novel methodology for the design of hydrogen peroxide-related biosensors by the formation or consumption of hydrogen peroxide. Using biotin-labeled DNA as capture probe, a model biosensor was proposed by immobilizing the probe on a nanosheet-modified electrode to recognize target DNA in the presence of an assistant DNA, which produced a "Y" junction structure to trigger a restriction endonuclease-aided target recycling. The target recycling resulted in the release of biotin labeled to the immobilized DNA from the nanosheet-modified electrode, thus decreased the consumption of hydrogen peroxide by horseradish peroxidase-mediated electrochemical reduction after binding the left biotin with horseradish peroxidase-labeled streptavidin, which produced an increasing photoelectrochemical response. The 'signal on' strategy for photoelectrochemical detection of DNA showed a low detection limit down to the subfemtomole level and good specificity to single-base mismatched oligonucleotides. The sensitized porous ZnO nanosheets are promising for applications in both photovoltaic devices and photoelectrochemical biosensing.

摘要

本工作报道了通过以(3-氨丙基)三乙氧基硅烷作为连接剂的共价结合方法合成新型CdTe量子点(QD)功能化的多孔ZnO纳米片。由于多孔结构以及CdTe量子点与ZnO纳米片之间合适的能带排列,功能化纳米片表现出优异的可见光吸收能力以及比CdTe量子点和ZnO纳米片都高得多的光电化学活性。以过氧化氢作为电子受体,纳米片修饰电极表现出灵敏的光电流响应。这一特性导致了一种通过过氧化氢的生成或消耗来设计与过氧化氢相关的生物传感器的新方法。使用生物素标记的DNA作为捕获探针,通过将探针固定在纳米片修饰电极上以在辅助DNA存在下识别靶DNA,提出了一种模型生物传感器,其产生“Y”形连接结构以触发限制性内切酶辅助的靶循环。靶循环导致固定在纳米片修饰电极上的生物素标记DNA释放生物素,因此在将剩余生物素与辣根过氧化物酶标记的链霉亲和素结合后,辣根过氧化物酶介导的电化学还原消耗的过氧化氢减少,从而产生增加的光电化学响应。用于DNA光电化学检测的“信号开启”策略显示出低至亚飞摩尔水平的检测限以及对单碱基错配寡核苷酸的良好特异性。敏化的多孔ZnO纳米片在光伏器件和光电化学生物传感方面都具有应用前景。

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