首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Synthesis and sensing integration: A novel enzymatic reaction modulated Nanoclusters Beacon (NCB) 'Illumination' strategy for label-free biosensing and logic gate operation
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Synthesis and sensing integration: A novel enzymatic reaction modulated Nanoclusters Beacon (NCB) 'Illumination' strategy for label-free biosensing and logic gate operation

机译:合成和传感集成:一种新颖的酶促反应纳米簇信标(NCB)“照明”策略,用于无标签生物传感和逻辑门操作

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A novel fluorescent label-free "turn-on" NAD(+) and adenosine triphosphate (ATP) biosensing strategy is proposed by fully exploiting ligation triggered Nanocluster Beacon (NCB). In the presence of the target, the split NCB was brought to intact, which brought the C-rich sequence and enhancer sequence in close proximity resulting in the lightening of dark DNA/AgNCs ("On" mode). Further application was presented for logic gate operation and aptasensor construction. The feasibility was investigated by Ultraviolet visible spectroscopy (UV-vis), Fluorescence, lifetime and High Resolution Transmission Electron Microscopy (HRTEM) etc. The strategy displayed good performance in the detection of NAD(+) and ATP, with the detection limit of 0.002 nM and 0.001 mM, the linear range of 10-1000 nM and 0.003-0.01 mM, respectively. Due to the DNA/AgNCs as fluorescence reporter, the completely label-free fluorescent strategy boasts the features of simplicity and low cost, and showing little reliance on the sensing environment. Meanwhile, the regulation by overhang G-rich sequence not relying on Forster energy transfer quenching manifests the high signal-to-background ratios (S/B ratios). This method not only provided a simple, economical and reliable fluorescent NAD(+) assay but also explored a flexible G-rich sequence regulated NCB probe for the fluorescent biosensors. Furthermore, this sensing mode was expanded to the application of a logic gate design, which exhibited a high performance for not only versatile biosensors construction but also for molecular computing application. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过充分利用连接触发的纳米簇信标(NCB),提出了一种新型的无荧光标记的“开启” NAD(+)和三磷酸腺苷(ATP)生物传感策略。在存在靶标的情况下,使裂解的NCB保持完整,使富含C的序列和增强子序列紧密相邻,从而使深色DNA / AgNC变亮(“打开”模式)。提出了逻辑门操作和适体传感器构造的进一步应用。通过紫外可见光谱(UV-vis),荧光,寿命和高分辨率透射电子显微镜(HRTEM)等方法研究了该可行性。该策略在NAD(+)和ATP的检测中表现出良好的性能,检出限为0.002 nM和0.001 mM,线性范围分别为10-1000 nM和0.003-0.01 mM。由于DNA / AgNCs作为荧光报告基因,完全无标记的荧光策略具有简单,成本低的特点,并且几乎不依赖传感环境。同时,通过不依赖Forster能量转移淬灭的富G突出端序列的调控显示出高的信号背景比(S / B比)。该方法不仅提供了一种简单,经济,可靠的荧光NAD(+)分析方法,而且还为荧光生物传感器探索了一种灵活的,富含G序列调控的NCB探针。此外,该感测模式已扩展到逻辑门设计的应用,该逻辑门不仅对通用生物传感器构造而且在分子计算应用中均表现出高性能。 (C)2016 Elsevier B.V.保留所有权利。

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