Single nucleobase identification for transversally-confined ssDNA using longitudinal ionic currents
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Updated: Sep 26, 2025

Studying DNA Looping by Single-Molecule FRET
Published on: June 28, 2014
Lijun Meng1, Jianxiang Huang1, Zhi He1
1Institute of Quantitative Biology, Shanghai Institute for Advanced Study, College of Life Sciences, and Department of Physics, Zhejiang University, Hangzhou 310027, China. rhzhou@zju.edu.cn.
Abstract:
High-fidelity DNA sequencing using solid-state nanopores remains a big challenge, partly due to difficulties related to efficient molecular capture and subsequent control of the dwell time. To help address these issues, here we propose a sequencing platform consisting of stacked two-dimensional materials with tailored structures containing a funnel-shaped step defect and a nanopore drilled inside the nanochannel. Our all-atom molecular dynamics (MD) simulations showed that, assisted by the step defect, single-stranded DNA (ssDNA) can be transported to the nanopore in a deterministic way by pulsed transversal electric fields. Furthermore, different types of DNA bases can reside in the pore for a sufficiently long time which can be successfully differentiated by longitudinal ionic currents. By using the decoupled driving forces for ssDNA transport and ionic current measurements, this approach holds potential for high-fidelity DNA sequencing.
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