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Current Enhancement in Solid-State Nanopores Depends on Three-Dimensional DNA Structure.

Vivian Wang1, Niklas Ermann1, Ulrich F Keyser1

  • 1Cavendish Laboratory , University of Cambridge , 19 JJ Thomson Avenue , Cambridge CB3 0HE , United Kingdom.

Nano Letters
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DNA translocation through nanopores shows concentration-dependent current changes. Bundled DNA nanostructures exhibit a lower crossover ionic concentration, impacting ion transport and nanopore sensing development.

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Area of Science:

  • Nanotechnology
  • Biophysics
  • Materials Science

Background:

  • Ionic current through solid-state nanopores is sensitive to DNA translocation.
  • The ionic concentration of the solution dictates whether DNA translocation causes current blockade or enhancement.
  • Understanding ion-molecule interactions in confined geometries is crucial for nanopore applications.

Purpose of the Study:

  • To investigate the ionic concentration-dependent translocation behavior of bundled DNA nanostructures.
  • To explore the influence of molecular structure on counterion mobility near DNA.
  • To assess the effect of neutral polymers on DNA translocation at low salt concentrations.

Main Methods:

  • Solid-state nanopore measurements of double-stranded DNA and bundled DNA nanostructures.
  • Systematic variation of ionic concentrations in the surrounding solution.
  • Introduction of neutral polymers (polyethylene glycol) to modify solution properties.

Main Results:

  • The crossover ionic concentration for bundled DNA nanostructures is lower than for double-stranded DNA.
  • Reduced counterion mobility near DNA is suggested, dependent on the molecule's 3D structure.
  • Polyethylene glycol addition facilitated translocation of large DNA structures at low salt concentrations by reducing electroosmotic outflow.

Conclusions:

  • The 3D structure of DNA nanostructures significantly influences ion transport dynamics in nanopores.
  • Modulating solution properties with neutral polymers can enhance nanopore translocation capabilities.
  • These findings advance the understanding of confined ion transport, aiding nanopore sensing and synthetic channel development.