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具有不同表面性质的核酸生物传感器中单链 DNA 的动力学和分子相互作用。

Dynamics and molecular interactions of single-stranded DNA in nucleic acid biosensors with varied surface properties.

机构信息

Department of Chemistry, University of California, Riverside, Riverside, CA 92521, USA.

出版信息

Phys Chem Chem Phys. 2019 Aug 7;21(29):16367-16380. doi: 10.1039/c9cp02441g. Epub 2019 Jul 16.

DOI:10.1039/c9cp02441g
PMID:31309941
Abstract

Electrochemical DNA biosensors utilizing self-assembled monolayers (SAMs) with inserted DNA probes are promising biosensor designs because of their ease of preparation, miniaturization, and tunability. However, much is still unknown about the interactions between biomolecules such as DNA and various surfaces. A fundamental question regarding these sensors concerns the nature of diffusion of target molecules taking place on sensor surfaces and whether it speeds up the molecular recognition process. Lack of understanding of molecular interaction and surface diffusion in addition to questions regarding the behavior of DNA probes immobilized on these surfaces currently limits the rational design of nucleic acid biosensors. Using all-atom unbiased molecular dynamics (MD) simulations we found that single-stranded DNA (ssDNA) behavior on SAMs is drastically altered by different surface chemistries, with ssDNA adopting very different orientations upon adsorption and surface diffusivity varying over an order of magnitude. Probe behavior varies equally broadly as probes are considerably more stable in certain SAMs than others, which affects the accessibility of probes to the target molecules and likely changes DNA hybridization kinetics in multiple ways. We also found that nearby probes can alter each other's orientations substantially, which highlights the importance of surface density control. Our results elucidate nucleic acid biosensor dynamics vital to rational design and offer insights that can aid in the design of surface properties and patterning for specific applications.

摘要

基于自组装单分子层(SAMs)的电化学 DNA 生物传感器具有制备简单、小型化和可调谐等优点,是很有前途的生物传感器设计。然而,对于 DNA 等生物分子与各种表面之间的相互作用,我们仍知之甚少。这些传感器的一个基本问题是关于目标分子在传感器表面上的扩散性质,以及它是否会加速分子识别过程。除了关于固定在这些表面上的 DNA 探针的行为的问题之外,对分子相互作用和表面扩散的缺乏理解目前限制了核酸生物传感器的合理设计。通过使用全原子无偏分子动力学(MD)模拟,我们发现单链 DNA(ssDNA)在 SAMs 上的行为由于不同的表面化学性质而发生了剧烈变化,ssDNA 在吸附时采用了非常不同的取向,表面扩散率也发生了数量级的变化。探针的行为同样广泛变化,因为在某些 SAMs 中探针比其他探针稳定得多,这会影响探针对目标分子的可及性,并可能以多种方式改变 DNA 杂交动力学。我们还发现,附近的探针可以显著改变彼此的取向,这突出了表面密度控制的重要性。我们的研究结果阐明了核酸生物传感器动力学对合理设计至关重要,并提供了可以帮助设计特定应用的表面性质和图案的见解。

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