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基于 DNA 的超分辨率光学光刻技术。

Super-Resolution Optical Lithography with DNA.

机构信息

Department of Chemistry , The Pennsylvania State University , University Park , Pennsylvania 16802 , United States.

出版信息

Nano Lett. 2019 Sep 11;19(9):6035-6042. doi: 10.1021/acs.nanolett.9b01873. Epub 2019 Aug 21.

DOI:10.1021/acs.nanolett.9b01873
PMID:31425652
Abstract

We developed an efficient, versatile, and accessible super-resolution microscopy method to construct a nanoparticle assembly at a spatial resolution below the optical diffraction limit. The method utilizes DNA and a photoactivated DNA cross-linker. Super-resolution optical techniques have been used only as a means to make measurements below the light diffraction limit. Furthermore, no optical technique is currently available to construct nanoparticle assemblies with a precisely designed shape and internal structure at a resolution of a few tens of nanometers (nm). Here we demonstrate that we can fulfill this deficiency by utilizing spontaneous structural dynamics of DNA hairpins combined with single-molecule fluorescence resonance energy transfer (smFRET) microscopy and a photoactivated DNA cross-linker. The stochastic fluorescence blinking due to the spontaneous folding and unfolding motions of DNA hairpins enables us to precisely localize a folded hairpin and solidify it only when it is within a predesigned target area whose size is below the diffraction limit. As the method is based on an optical microscope and an easily clickable DNA cross-linking reagent, it will provide an efficient means to create large nanoparticle assemblies with a shape and internal structure at an optical super-resolution, opening a wide window of opportunities toward investigating their photophysical and optoelectronic properties and developing novel devices.

摘要

我们开发了一种高效、通用且易于使用的超分辨率显微镜方法,可在低于光学衍射极限的空间分辨率下构建纳米颗粒组装体。该方法利用了 DNA 和光活化的 DNA 交联剂。超分辨率光学技术仅被用作在光衍射极限以下进行测量的手段。此外,目前没有光学技术可用于以几十纳米(nm)的分辨率构建具有精确设计形状和内部结构的纳米颗粒组装体。在这里,我们证明我们可以通过利用 DNA 发夹的自发结构动力学以及单分子荧光共振能量转移(smFRET)显微镜和光活化的 DNA 交联剂来弥补这一不足。由于 DNA 发夹的自发折叠和展开运动而产生的随机荧光闪烁使我们能够精确地定位折叠的发夹,并仅在其处于预定的目标区域内时将其固定,该目标区域的大小低于衍射极限。由于该方法基于光学显微镜和易于点击的 DNA 交联试剂,因此它将提供一种有效的方法来以光学超分辨率创建具有形状和内部结构的大型纳米颗粒组装体,为研究其光物理和光电性质以及开发新型器件开辟了广阔的机会。

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Super-Resolution Optical Lithography with DNA.基于 DNA 的超分辨率光学光刻技术。
Nano Lett. 2019 Sep 11;19(9):6035-6042. doi: 10.1021/acs.nanolett.9b01873. Epub 2019 Aug 21.
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Conformational dynamics of DNA hairpins at millisecond resolution obtained from analysis of single-molecule FRET histograms.从单分子 FRET 直方图分析中获得的纳秒分辨率下 DNA 发夹的构象动力学。
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Correlative Single-Molecule FRET and DNA-PAINT Imaging.相关单分子 FRET 和 DNA-PAINT 成像。
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