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Exploration of the Kinetics of Toehold Mediated Strand Displacement via Plasmon Rulers

机译:通过等离子体尺寸探索脚趾介导的绞线位移的动力学

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摘要

DNA/RNA strand displacement is one of the most fundamental reactions in DNA and RNA circuits and nanomachines. In this work, we reported an exploration of the dynamic process of the toehold-mediated strand displacement via core satellite plasmon rulers at the single-molecule level. Applying plasmon rulers with unlimited lifetime, single-strand displacement triggered by the invader that resulted in stepwise leaving of satellite from the core was continuously monitored by changes of scattering signal for hours. The kinetics of strand displacement in vitro with three different toehold lengths have been investigated. Also, the study revealed the difference in the kinetics of strand displacement between DNA/RNA and DNA/DNA duplexes. For the kinetics study in vivo, influence from the surrounding medium has been evaluated using both phosphate buffer and cell lysate. Applying core satellite plasmon rulers with high signal/noise ratio, kinetics study in living cells proceeded for the first time, which was not possible by conventional methods with a fluorescent reporter. The plasmon rulers, which are flexible, easily constructed, and robust, have proven to be effective tools in exploring the dynamical behaviors of biochemical reactions in vivo.
机译:DNA / RNA链位移是DNA和RNA电路和纳米载体中最基本的反应之一。在这项工作中,我们报道了通过在单分子水平的核心卫星等离子体尺寸通过核心卫星等离子体统治者探讨了荷摩介导的链位移的动态过程。用无限寿命应用等离子体统治者,由侵略者触发的单链位移,通过散射信号的变化连续监测从核心逐步离开卫星的透射卫星。研究了三种不同的TOEhold长度体外体外排水量的动力学。此外,该研究揭示了DNA / RNA和DNA双链体之间链位移的动力学差异。对于体内的动力学研究,已经使用磷酸盐缓冲液和细胞裂解物评估了周围培养基的影响。应用具有高信号/噪声比的核心卫星等离子体统治者,活性细胞的动力学研究第一次进行,常规方法与荧光报告器不可能进行。柔性,易于构造和坚固的等离子体统治者已被证明是探索体内生化反应的动态行为的有效工具。

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