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Probing Electron-Induced Bond Cleavage at the Single-Molecule Level Using DNA Origami Templates

机译:使用DNA折纸模板在单分子水平上探测电子诱导的键裂解

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Low-energy electrons (LEEs) play an important role in nanolithography, atmospheric chemistry, and DNA radiation damage. Previously, the cleavage of specific chemical bonds triggered by LEEs has been demonstrated in a variety of small organic molecules such as halogenated benzenes and DNA nucleobases. Here we present a strategy that allows for the first time to visualize the electron-induced dissociation of single chemical bonds within complex, but well-defined self-assembled DNA nanostructures. We employ atomic force microscopy to image and quantify LEE-induced bond dissociations within specifically designed oligonucleotide targets that are attached to DNA origami templates. In this way, we use a highly selective approach to compare the efficiency of the electron-induced dissociation of a single disulfide bond with the more complex cleavage of the DNA backbone within a TT dinucleotide sequence. This novel technique enables the fast and parallel determination of DNA strand break yields with unprecedented control over the DNA's primary and secondary structure. Thus the detailed investigation of DNA radiation damage in its most natural environment, e.g., DNA nucleosomes constituting the chromatin, now becomes feasible.
机译:低能电子(LEE)在纳米光刻,大气化学和DNA辐射损伤中起着重要作用。以前,由LEES引发的特定化学键的裂解已在各种小的有机分子(如卤代苯和DNA核碱基)中得到证明。在这里,我们提出一种策略,首次使可视化复杂但定义明确的自组装DNA纳米结构内单个化学键的电子诱导解离。我们采用原子力显微镜对附着在DNA折纸模板上的特别设计的寡核苷酸靶标内的LEE诱导的键解离进行成像和定量。通过这种方式,我们使用高度选择性的方法比较单个二硫键的电子诱导解离与TT二核苷酸序列中DNA骨架的更复杂裂解的效率。这项新技术可以对DNA的一级和二级结构进行空前的控制,从而能够快速,并行地确定DNA链断裂的产量。因此,在其最自然的环境中,例如构成染色质的DNA核小体的DNA辐射损伤的详细研究现在变得可行。

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