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使用多参数单分子荧光共振能量转移对DNA链置换进行子集合监测。

Sub-Ensemble Monitoring of DNA Strand Displacement Using Multiparameter Single-Molecule FRET.

作者信息

Baltierra-Jasso Laura E, Morten Michael J, Magennis Steven W

机构信息

WestCHEM School of Chemistry, University of Glasgow, University Avenue, Glasgow, G12 8QQ, UK.

出版信息

Chemphyschem. 2018 Mar 5;19(5):551-555. doi: 10.1002/cphc.201800012. Epub 2018 Jan 26.

Abstract

Non-enzymatic DNA strand displacement is an important mechanism in dynamic DNA nanotechnology. Here, we show that the large parameter space that is accessible by single-molecule FRET is ideal for the simultaneous monitoring of multiple reactants and products of DNA strand exchange reactions. We monitored the strand displacement from double-stranded DNA (dsDNA) by single-stranded DNA (ssDNA) at 37 °C; the data were modelled as a second-order reaction approaching equilibrium, with a rate constant of 10 m  s . We also followed the displacement from a DNA three-way junction (3WJ) by ssDNA. The presence of three internal mismatched bases in the middle of the invading strand did not prevent displacement from the 3WJ, but reduced the second-order rate constant by about 50 %. We attribute strand exchange in the dsDNA and 3WJ to a zero-toehold pathway from the blunt-ended duplex arms. The single-molecule approach demonstrated here will be useful for studying complex DNA networks.

摘要

非酶促DNA链置换是动态DNA纳米技术中的一种重要机制。在此,我们表明单分子荧光共振能量转移(FRET)可及的大参数空间非常适合同时监测DNA链交换反应的多种反应物和产物。我们在37°C下监测了单链DNA(ssDNA)对双链DNA(dsDNA)的链置换;数据被建模为接近平衡的二级反应,速率常数为10 m⁻¹ s⁻¹。我们还追踪了ssDNA对DNA三向接头(3WJ)的置换。侵入链中间存在三个内部错配碱基并不妨碍从3WJ进行置换,但使二级速率常数降低了约50%。我们将dsDNA和3WJ中的链交换归因于来自平头双链臂的零起始途径。本文展示的单分子方法将有助于研究复杂的DNA网络。

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