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单分子 DNA 杂交动力学的单碱基分辨率直接测量。

Direct Measurement of Single-Molecule DNA Hybridization Dynamics with Single-Base Resolution.

机构信息

Key Laboratory of Radiopharmaceuticals, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing, 100875, P.R. China.

Beijing National Laboratory for Molecular Sciences, State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, P.R. China.

出版信息

Angew Chem Int Ed Engl. 2016 Jul 25;55(31):9036-40. doi: 10.1002/anie.201603038. Epub 2016 Jun 8.

Abstract

Herein, we report label-free detection of single-molecule DNA hybridization dynamics with single-base resolution. By using an electronic circuit based on point-decorated silicon nanowires as electrical probes, we directly record the folding/unfolding process of individual hairpin DNAs with sufficiently high signal-to-noise ratio and bandwidth. These measurements reveal two-level current oscillations with strong temperature dependence, enabling us to determine the thermodynamic and kinetic properties of hairpin DNA hybridization. More importantly, successive, stepwise increases and decreases in device conductance at low temperature on a microsecond timescale are successfully observed, indicating a base-by-base unfolding/folding process. The process demonstrates a kinetic zipper model for DNA hybridization/dehybridization at the single base-pair level. This measurement capability promises a label-free single-molecule approach to probe biomolecular interactions with fast dynamics.

摘要

在此,我们报告了一种无标记的单分子 DNA 杂交动力学检测方法,具有单碱基分辨率。通过使用基于点修饰硅纳米线的电子电路作为电探针,我们直接记录了单个发夹 DNA 的折叠/展开过程,具有足够高的信噪比和带宽。这些测量结果显示出具有强温度依赖性的两级电流振荡,使我们能够确定发夹 DNA 杂交的热力学和动力学性质。更重要的是,在微秒时间尺度上,我们成功地观察到低温下器件电导的连续、逐步增加和减少,表明了碱基对的展开/折叠过程。该过程展示了在单个碱基对水平上 DNA 杂交/去杂交的动力学拉链模型。这种测量能力有望提供一种无标记的单分子方法,用于探测具有快速动力学的生物分子相互作用。

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