Qian Weixin, Doi Kentaro, Kawano Satoyuki
Department of Mechanical Science and Bioengineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka, Japan.
Department of Mechanical Science and Bioengineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama, Toyonaka, Osaka, Japan.
Biophys J. 2017 Mar 14;112(5):838-849. doi: 10.1016/j.bpj.2017.01.027.
Electrokinetic phenomena in micro/nanofluidic channels have attracted considerable attention because precise control of molecular transport in liquids is required to optically and electrically capture the behavior of single molecules. However, the detailed mechanisms of polymer transport influenced by electroosmotic flows and electric fields in micro/nanofluidic channels have not yet been elucidated. In this study, a Langevin dynamics simulation was used to investigate the electrokinetic transport of single-stranded DNA (ssDNA) in a cylindrical nanochannel, employing a coarse-grained bead-spring model that quantitatively reproduced the radius of gyration, diffusion coefficient, and electrophoretic mobility of the polymer. Using this practical scale model, transport regimes of ssDNA with respect to the ζ-potential of the channel wall, the ion concentration, and the polymer length were successfully characterized. It was found that the relationship between the radius of gyration of ssDNA and the channel radius is critical to the formation of deformation regimes in a narrow channel. We conclude that a combination of electroosmotic flow velocity gradients and electric fields due to electrically polarized channel surfaces affects the alignment of molecular conformations, such that the ssDNA is stretched/compressed at negative/positive ζ-potentials in comparatively low-concentration solutions. Furthermore, this work suggests the possibility of controlling the center-of-mass position by tuning the salt concentration. These results should be applicable to the design of molecular manipulation techniques based on liquid flows in micro/nanofluidic devices.
微纳流体通道中的电动现象引起了广泛关注,因为要通过光学和电学手段捕捉单分子行为,就需要精确控制液体中的分子传输。然而,微纳流体通道中电渗流和电场对聚合物传输的详细机制尚未阐明。在本研究中,我们使用朗之万动力学模拟来研究单链DNA(ssDNA)在圆柱形纳米通道中的电动传输,采用粗粒化的珠簧模型,该模型能定量再现聚合物的回转半径、扩散系数和电泳迁移率。利用这个实际尺度模型,成功地确定了ssDNA在通道壁ζ电位、离子浓度和聚合物长度方面的传输状态。研究发现,ssDNA的回转半径与通道半径之间的关系对于在狭窄通道中形成变形状态至关重要。我们得出结论,由于通道表面的电极化而产生的电渗流速度梯度和电场的组合会影响分子构象的排列,使得在相对低浓度溶液中,ssDNA在负/正ζ电位下被拉伸/压缩。此外,这项工作表明通过调节盐浓度来控制质心位置的可能性。这些结果应适用于基于微纳流体装置中液体流动的分子操纵技术的设计。