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基于随机开关定位显微镜的单 DNA 分子传感器的亚衍射成像。

Toward Sub-Diffraction Imaging of Single-DNA Molecule Sensors Based on Stochastic Switching Localization Microscopy.

机构信息

Department of Applied Chemistry and Institute of Natural Sciences, Kyung Hee University, Yongin-si, Gyeonggi-do 17104, Korea.

出版信息

Sensors (Basel). 2020 Nov 21;20(22):6667. doi: 10.3390/s20226667.

Abstract

The natural characteristics of deoxyribonucleic acid (DNA) enable its advanced applications in nanotechnology as a special tool that can be detected by high-resolution imaging with precise localization. Super-resolution (SR) microscopy enables the examination of nanoscale molecules beyond the diffraction limit. With the development of SR microscopy methods, DNA nanostructures can now be optically assessed. Using the specific binding of fluorophores with their target molecules, advanced single-molecule localization microscopy (SMLM) has been expanded into different fields, allowing wide-range detection at the single-molecule level. This review discusses the recent progress in the SR imaging of DNA nano-objects using SMLM techniques, such as direct stochastic optical reconstruction microscopy, binding-activated localization microscopy, and point accumulation for imaging nanoscale topography. Furthermore, we discuss their advantages and limitations, present applications, and future perspectives.

摘要

脱氧核糖核酸(DNA)的自然特性使其在纳米技术中作为一种特殊工具得到了广泛应用,这种工具可以通过高分辨率成像进行精确定位检测。超分辨率(SR)显微镜使我们能够检查超越衍射极限的纳米级分子。随着 SR 显微镜方法的发展,现在可以对 DNA 纳米结构进行光学评估。利用荧光染料与靶分子的特异性结合,先进的单分子定位显微镜(SMLM)已扩展到不同领域,能够在单分子水平上进行广泛的检测。本文综述了使用 SMLM 技术对 DNA 纳米物体进行 SR 成像的最新进展,如直接随机光学重建显微镜、结合激活定位显微镜和点积累用于成像纳米级形貌。此外,我们还讨论了它们的优缺点、应用和未来展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af7d/7700606/73d33f1fe5ff/sensors-20-06667-g001.jpg

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