Ma B O, Kim Jin-Woo, Tung Steve
Department of Mechanical Engineering, University of Arkansas, Fayetteville, AR 72701 USA.
Department of Biological & Agricultural Engineering, University of Arkansas, Fayetteville, AR 72701 USA.
IEEE Open J Nanotechnol. 2022;3:124-130. doi: 10.1109/ojnano.2022.3217108. Epub 2022 Oct 25.
Precision DNA translocation control is critical for achieving high accuracy in single molecule-based DNA sequencing. In this report, we describe an atomic force microscopy (AFM) based method to linearize a double-stranded DNA strand during the translocation process and characterize the electrical properties of the moving DNA using a platinum (Pt) nanoelectrode gap. In this method, DNAs were first deposited on a charged mica substrate surface and topographically scanned. A single DNA suitable for translocation was then identified and electrostatically attached to an AFM probe by pressing the probe tip down onto one end of the DNA strand without chemical functionalizations. Next, the DNA strand was lifted off the mica surface by the probe tip. The pulling force required to completely lift off the DNA agreed well with the theoretical DNA adhesion force to a charged mica surface. After liftoff, the captured DNA was translocated at varied speeds across the substrate and ultimately across the Pt nanoelectrode gap for electrical characterizations. Finally, finite element analysis of the effect of the translocating DNA on the conductivity of the nanoelectrode gap was conducted, validating the range of the gap current measured experimentally during the DNA translocation process.
精确的DNA易位控制对于基于单分子的DNA测序实现高精度至关重要。在本报告中,我们描述了一种基于原子力显微镜(AFM)的方法,用于在易位过程中使双链DNA链线性化,并使用铂(Pt)纳米电极间隙表征移动DNA的电学性质。在该方法中,首先将DNA沉积在带电荷的云母基底表面并进行形貌扫描。然后识别出适合易位的单个DNA,并通过将探针尖端压在DNA链的一端而无需化学功能化,将其静电附着到AFM探针上。接下来,通过探针尖端将DNA链从云母表面提起。完全提起DNA所需的拉力与理论上DNA对带电荷云母表面的粘附力非常吻合。提起后,捕获的DNA以不同速度在基底上移动,并最终穿过Pt纳米电极间隙进行电学表征。最后,对易位DNA对纳米电极间隙电导率的影响进行了有限元分析,验证了DNA易位过程中实验测量的间隙电流范围。