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首页> 外文期刊>Biopolymers: Original Research on Biomolecules and Biomolecular Assemblies >DNA and chromatin imaging with super-resolution fluorescence microscopy based on single-molecule localization
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DNA and chromatin imaging with super-resolution fluorescence microscopy based on single-molecule localization

机译:基于单分子定位的超高分辨率荧光显微镜对DNA和染色质成像

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摘要

With the expansion of super-resolution fluorescence microscopy methods, it is now possible to access the organization of cells and materials at the nanoscale by optical means. This review discusses recent progress in super-resolution imaging of isolated and cell DNA using single-molecule localization methods. A high labeling density of photoswitchable fluorophores is crucial for these techniques, which can be provided by sequence independent DNA stains in which photoblinking reactions can be induced. In particular, unsymmetrical cyanine intercalating dyes in combination with special buffers can be used to image isolated DNA with a spatial resolution of 30-40 nm. For super-resolution imaging of chromatin, cell permeant cyanine dyes that bind the minor groove of DNA have the potential to become a useful alternative to the labeling of histones and other DNA-associated proteins. Other recent developments that are interesting in this context such as high density labeling methods or new DNA probes with photoswitching functionalities are also surveyed. Progress in labeling, optics, and single-molecule localization algorithms is being rapid, and it is likely to provide real insight into DNA structuring in cells and materials.
机译:随着超分辨率荧光显微镜方法的扩展,现在可以通过光学手段进入纳米尺度的细胞和材料组织。这篇综述讨论了使用单分子定位方法对分离的DNA和细胞DNA进行超分辨率成像的最新进展。对这些技术而言,光可转换荧光团的高标记密度至关重要,这可以通过不依赖序列的DNA染色剂来提供,在其中可以诱导光闪烁反应。特别是,不对称的花青插层染料与特殊的缓冲液结合可用于以30-40 nm的空间分辨率对分离的DNA进行成像。对于染色质的超分辨率成像,结合DNA小沟的细胞渗透性花青染料有可能成为组蛋白和其他DNA相关蛋白标记的有用替代方法。在这方面有趣的其他最新进展,例如高密度标记方法或具有光开关功能的新型DNA探针也得到了调查。标记,光学和单分子定位算法的进展非常迅速,很可能为细胞和材料中的DNA结构提供真正的见识。

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