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Intercalation-Based Single-Molecule Fluorescence Assay To Study DNA Supercoil Dynamics

机译:基于插层的单分子荧光测定法研究DNA超螺旋动力学

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摘要

DNA supercoiling crucially affects cellular processes such as DNA replication, gene expression, and chromatin organization. However, mechanistic understanding of DNA supercoiling and the related DNA-processing enzymes has remained limited, mainly due to the lack of convenient experimental tools to probe these phenomena. Here, we report a novel high-throughput single-molecule assay for real-time visualization of supercoiled DNA molecules, named ISD (Intercalation-induced Supercoiling of DNA). We use an intercalating dye to induce supercoiling of surface-attached DNA molecules as well as to visualize coiled-loop structures (i.e., plectonemes) formed on DNA. The technique is solely based on epifluorescence microscopy and requires no mechanical manipulation of the DNA molecules. This new assay allows to track positions and sizes of individual plectonemes and characterize their position-dependent dynamics such as nucleation, termination, and diffusion. We describe the ISD technique and demonstrate its potential by establishing that plectonemes are pinned to a local 10-nucleotide long mispaired sequence along a double-stranded DNA molecule.
机译:DNA超螺旋至关重要地影响细胞过程,例如DNA复制,基因表达和染色质组织。但是,对DNA超螺旋和相关的DNA加工酶的机理了解仍然很有限,这主要是由于缺乏方便的实验工具来探测这些现象。在这里,我们报告了一种新颖的高通量单分子测定法,用于实时可视化超螺旋DNA分子,称为ISD(插入诱导的DNA超螺旋)。我们使用一种嵌入染料来诱导表面附着的DNA分子的超螺旋作用,并可视化在DNA上形成的螺旋环结构(即Plectoneme)。该技术仅基于落射荧光显微镜,不需要对DNA分子进行机械操作。这项新的测定方法可以追踪各个plectoneme的位置和大小,并表征其与位置有关的动力学,例如成核,终止和扩散。我们描述了ISD技术,并通过建立Plectoneme固定于沿双链DNA分子的局部10核苷酸长错配序列而证明了其潜力。

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