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首页> 外文期刊>Nature nanotechnology >A plasmonic 'antenna-in-box' platform for enhanced single-molecule analysis at micromolar concentrations
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A plasmonic 'antenna-in-box' platform for enhanced single-molecule analysis at micromolar concentrations

机译:用于在微摩尔浓度下增强单分子分析的等离激元“盒内天线”平台

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摘要

Single-molecule fluorescence techniques are key for a number of applications, including DNA sequencing, molecular and cell biology and early diagnosis. Unfortunately, observation of single molecules by diffraction-limited optics is restricted to detection volumes in the femtolitre range and requires pico- or nanomolar concentrations, far below the micromolar range where most biological reactions occur. This limitation can be overcome using plasmonic nanostructures, which enable the confinement of light down to nanoscale volumes. Although these nanoantennas enhance fluorescence brightness, large background signals and/or unspecific binding to the metallic surface have hampered the detection of individual fluorescent molecules in solution at high concentrations. Here we introduce a novel 'antenna-in-box' platform that is based on a gap-antenna inside a nanoaperture. This design combines fluorescent signal enhancement and background screening, offering high single-molecule sensitivity (fluorescence enhancement up to 1,100-fold and microsecond transit times) at micromolar sample concentrations and zeptolitre-range detection volumes. The antenna-in-box device can be optimized for single-molecule fluorescence studies at physiologically relevant concentrations, as we demonstrate using various biomolecules.
机译:单分子荧光技术是许多应用的关键,包括DNA测序,分子和细胞生物学以及早期诊断。不幸的是,通过衍射极限光学仪器观察单个分子仅限于飞摩尔范围内的检测体积,并且需要皮摩尔或纳摩尔浓度,远低于大多数生物反应发生的微摩尔范围。使用等离子纳米结构可以克服这种局限性,该等离子纳米结构能够将光限制在纳米级以下。尽管这些纳米天线增强了荧光亮度,但是大背景信号和/或与金属表面的非特异性结合已阻碍了高浓度溶液中单个荧光分子的检测。在这里,我们介绍一种新颖的“盒内天线”平台,该平台基于纳米孔径内的间隙天线。该设计将荧光信号增强和背景筛选结合在一起,在微摩尔样品浓度和Zeptolitre范围检测体积下提供高单分子灵敏度(高达1100倍的荧光增强和微秒的传输时间)。正如我们使用各种生物分子所展示的,箱内天线设备可以针对生理相关浓度的单分子荧光研究进行优化。

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