Zhang Yuanshuo, Ding Mingming, Li Minglun, Shi Tongfei
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, People's Republic of China.
Jieyang Branch of Chemistry and Chemical Engineering, Guangdong Laboratory, Jieyang 515200, People's Republic of China.
J Phys Chem Lett. 2025 Jan 9;16(1):357-364. doi: 10.1021/acs.jpclett.4c03145. Epub 2024 Dec 30.
Efficient capture of single-stranded DNA (ssDNA) is crucial for high-throughput sequencing, which influences the speed and accuracy of genetic analysis. Electrophoresis (EP) and electro-osmotic flow (EOF) have a significant impact on the translocation behavior of ssDNA through the nanopore. Experimentally, dynamically tracking these two effects remains challenging, and conventional numerical methods also struggle to capture their dynamic properties in the presence of DNA. We use all-atom molecular dynamics (MD) simulations to study how do EP and EOF play a role in the capture of DNA under different surface charge densities and graphene layer numbers. Our findings indicate that positive surface charge densities work together with electrophoretic forces () to enhance the EOF, resulting in rapid and efficient ssDNA capture with improved rates of up to 88% and reduced capture times. Electro-osmotic force () substantially enhances capture efficiency by not only lowering the energy barrier for ssDNA translocation through the nanopore but also increasing the probability of ssDNA locating and aligning with the pore entrance. Negative charges create a repulsive electrostatic environment. Along with the opposing EOF, this lowers the chances of capture. Additionally, we found that an increased number of graphene layers can shield internal electric fields, affecting ssDNA capture negatively by tempering the effects of EOF. This research highlights the importance of precise control over nanopore surface charge and layers to optimize the performance of graphene nanopore sequencing technologies, offering potential avenues for significant advancements in genomic sequencing.
高效捕获单链DNA(ssDNA)对于高通量测序至关重要,这会影响基因分析的速度和准确性。电泳(EP)和电渗流(EOF)对ssDNA通过纳米孔的转运行为有重大影响。在实验中,动态跟踪这两种效应仍然具有挑战性,并且传统数值方法在存在DNA的情况下也难以捕捉它们的动态特性。我们使用全原子分子动力学(MD)模拟来研究在不同表面电荷密度和石墨烯层数下,EP和EOF如何在DNA捕获中发挥作用。我们的研究结果表明,正表面电荷密度与电泳力协同作用以增强EOF,从而实现快速高效的ssDNA捕获,捕获率提高高达88%,捕获时间缩短。电渗力不仅降低了ssDNA通过纳米孔的能量势垒,还增加了ssDNA定位并与孔入口对齐的概率,从而大大提高了捕获效率。负电荷会产生排斥性静电环境,连同相反的EOF一起,降低了捕获的机会。此外,我们发现增加石墨烯层数会屏蔽内部电场,通过减弱EOF的作用对ssDNA捕获产生负面影响。这项研究强调了精确控制纳米孔表面电荷和层数对于优化石墨烯纳米孔测序技术性能的重要性,为基因组测序的重大进展提供了潜在途径。