Department of Mechanical Engineering, University of Tokyo , Tokyo 113-8656, Japan.
Anal Chem. 2016 Sep 20;88(18):9251-8. doi: 10.1021/acs.analchem.6b02513. Epub 2016 Sep 9.
The control of biomolecule translocation through nanopores is important in nanopore protein detection. Improvement in current nanopore molecule control is desired to enhance capture rates, extend translocation times, and ensure the effective detection of various proteins in the same solutions. We present a method that simultaneously resolves these issues through the use of a gate-modulated conical nanopore coupled with solutions of varying salt concentration. Simulation results show that the presence of an induced reverse electroosmotic flow (IREOF) results in inlet flows from the two ends of the nanopore centerline entering into the nanopore in opposite directions, which simultaneously elevates the capture rate and immobilizes the protein in the nanopore, thus enabling steady current blockage measurements for a range of proteins. In addition, it is shown that proteins with different size/charge ratios can be trapped by a gate modulation intensified flow field at a similar location in the nanopore in the same solution conditions.
生物分子通过纳米孔的传输控制在纳米孔蛋白检测中非常重要。为了提高捕获率、延长传输时间,并确保在相同溶液中有效检测各种蛋白质,我们希望改进当前的纳米孔分子控制方法。我们提出了一种通过使用门调制锥形纳米孔结合不同盐浓度溶液来同时解决这些问题的方法。模拟结果表明,诱导反向电渗流(IREOF)的存在导致纳米孔中心线上的两个末端的入口流以相反的方向进入纳米孔,这同时提高了捕获率并将蛋白质固定在纳米孔中,从而可以对一系列蛋白质进行稳定的电流阻断测量。此外,结果表明,在相同溶液条件下,不同大小/电荷比的蛋白质可以在纳米孔中的相同位置被门调制强化流场捕获。