Wen Chenyu, Schmid Sonja, Dekker Cees
Department of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, Van der Maasweg 9, Delft 2629 HZ, The Netherlands.
Laboratory of Biophysics, Wageningen University and Research, Stippeneng 4, Wageningen 6708 WE, The Netherlands.
ACS Nano. 2024 Jul 25;18(31):20449-58. doi: 10.1021/acsnano.4c04788.
Nanopore technology is widely used for sequencing DNA, RNA, and peptides with single-molecule resolution, for fingerprinting single proteins, and for detecting metabolites. However, the molecular driving forces controlling the analyte capture, its residence time, and its escape have remained incompletely understood. The recently developed Nanopore Electro-Osmotic trap (NEOtrap) is well fit to study these basic physical processes in nanopore sensing, as it reveals previously missed events. Here, we use the NEOtrap to quantitate the electro-osmotic and electrophoretic forces that act on proteins inside the nanopore. We establish a physical model to describe the capture and escape processes, including the trapping energy potential. We verified the model with experimental data on CRISPR dCas9-RNA-DNA complexes, where we systematically screened crucial modeling parameters such as the size and net charge of the complex. Tuning the balance between electrophoretic and electro-osmotic forces in this way, we compare the trends in the kinetic parameters with our theoretical models. The result is a comprehensive picture of the major physical processes in nanopore trapping, which helps to guide the experiment design and signal interpretation in nanopore experiments.
纳米孔技术广泛用于以单分子分辨率对DNA、RNA和肽进行测序,对单个蛋白质进行指纹识别以及检测代谢物。然而,控制分析物捕获、其停留时间及其逃逸的分子驱动力仍未完全了解。最近开发的纳米孔电渗阱(NEOtrap)非常适合研究纳米孔传感中的这些基本物理过程,因为它揭示了以前遗漏的事件。在这里,我们使用NEOtrap来定量作用于纳米孔内蛋白质的电渗力和电泳力。我们建立了一个物理模型来描述捕获和逃逸过程,包括捕获能量势。我们用CRISPR dCas9-RNA-DNA复合物的实验数据验证了该模型,在该实验中我们系统地筛选了关键建模参数,如复合物的大小和净电荷。通过这种方式调整电泳力和电渗力之间的平衡,我们将动力学参数的趋势与我们的理论模型进行了比较。结果是对纳米孔捕获中主要物理过程的全面描述,这有助于指导纳米孔实验中的实验设计和信号解释。