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Sequence and Temperature Influence on Kinetics of DNA Strand Displacement at Gold Electrode Surfaces

机译:序列和温度对金电极表面DNA链置换动力学的影响

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Understanding complex contributions of surface environment to tethered nucleic acid sensing experiments has proven challenging, yet it is important because it is essential for interpretation and calibration of indispensable methods, such as microarrays. We investigate the effects of DNA sequence and solution temperature gradients on the kinetics of strand displacement at heated gold wire electrodes, and at gold disc electrodes in a heated solution. Addition of a terminal double mismatch (toehold) provides a reduction in strand displacement energy barriers sufficient to probe the secondary mechanisms involved in the hybridization process. In four different DNA capture probe sequences (relevant for the identification of genetically modified maize MON810), all but one revealed a high activation energy up to 200 kJ/mol during hybridization, that we attribute to displacement of protective strands by capture probes. Protective strands contain 4 to 5 mismatches to ease their displacement by the surface-confined probes at the gold electrodes. A low activation energy (30 kJ/mol) was observed for the sequence whose protective strand contained a toehold and one central mismatch, its kinetic curves displayed significantly different shapes, and we observed a reduced maximum signal intensity as compared to other sequences. These findings point to potential sequence-related contributions to oligonucleotide diffusion influencing kinetics. Additionally, for all sequences studied with heated wire electrodes, we observed a 23 K lower optimal hybridization temperature in comparison with disc electrodes in heated solution, and greatly reduced voltammetric signals after taking into account electrode surface area. We propose that thermodiffusion due to temperature gradients may influence both hybridization and strand displacement kinetics at heated microelectrodes, an explanation supported by computational fluid dynamics. DNA assays with surface-confined capture probes and temperature gradients should not neglect potential influences of thermodiffusion as well as sequence-related effects. Furthermore, studies attempting to characterize surface-tethered environments should consider thermodiffusion if temperature gradients are involved.
机译:理解表面环境对拴系核酸感测实验的复杂贡献已被证明具有挑战性,但这很重要,因为它对于解释和校准必不可少的方法(例如微阵列)至关重要。我们研究了DNA序列和溶液温度梯度对在加热的金丝电极上以及在加热溶液中的金盘电极上的链位移动力学的影响。末端双错配(toehold)的增加提供了足以探测杂交过程中涉及的二级机制的链位移能垒的降低。在四种不同的DNA捕获探针序列中(与鉴定转基因玉米MON810有关),除一个序列外,其余所有序列都显示出高达200 kJ / mol的高活化能,这归因于捕获探针置换了保护链。保护链包含4至5个错配,以减轻金电极上表面受限探针的位移。对于其保护链包含一个脚趾和一个中心错配的序列,观察到了较低的活化能(30 kJ / mol),其动力学曲线显示出明显不同的形状,并且与其他序列相比,我们观察到最大信号强度降低。这些发现表明对寡核苷酸扩散影响动力学的潜在的序列相关贡献。此外,对于在加热丝电极中研究的所有序列,与在加热溶液中的圆盘电极相比,我们观察到的最佳杂交温度低23 K,并且在考虑电极表面积后大大降低了伏安信号。我们提出,由于温度梯度引起的热扩散可能会影响杂交和加热的微电极上的链置换动力学,这是计算流体力学支持的一种解释。使用表面受限的捕获探针和温度梯度进行的DNA分析不应忽略热扩散的潜在影响以及与序列相关的影响。此外,如果涉及温度梯度,则试图表征表面束缚环境的研究应考虑热扩散。

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