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Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores
09:43

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Published on: October 31, 2013

Direct force measurements on double-stranded RNA in solid-state nanopores.

Michiel van den Hout1, Igor D Vilfan, Susanne Hage

  • 1Kavli Institute of Nanoscience, Faculty of Applied Sciences Delft University of Technology, Lorentzweg 1, 2628 CJ Delft. The Netherlands.

Nano Letters
|January 7, 2010
PubMed
Summary

This study introduces a novel nanopore-optical tweezers system for measuring forces on double-stranded RNA (dsRNA). The findings reveal how dsRNA force changes with nanopore size, offering new RNA research possibilities.

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Last Updated: Jun 17, 2026

Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores
09:43

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Published on: October 31, 2013

Dual DNA Rulers to Study the Mechanism of Ribosome Translocation with Single-Nucleotide Resolution
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Published on: July 8, 2019

Nanomanipulation of Single RNA Molecules by Optical Tweezers
06:59

Nanomanipulation of Single RNA Molecules by Optical Tweezers

Published on: August 20, 2014

Area of Science:

  • Biophysics
  • Molecular Biology
  • Nanotechnology

Background:

  • Solid-state nanopores enable single-molecule analysis via voltage-driven translocation.
  • Integrating optical tweezers enhances nanopore sensitivity and versatility for force measurements.

Purpose of the Study:

  • To demonstrate the first application of nanopore-optical tweezers for studying double-stranded RNA (dsRNA).
  • To measure the net force on individual dsRNA molecules across various nanopore sizes.
  • To compare the force on dsRNA with that on double-stranded DNA (dsDNA).

Main Methods:

  • Utilized a combined nanopore-optical tweezers system.
  • Translocated individual dsRNA molecules through nanopores ranging from 35 nm to 3.5 nm.
  • Measured the net force exerted on dsRNA during translocation.
  • Compared force measurements with dsDNA in identical nanopores.

Main Results:

  • The force on dsRNA decreases as nanopore size increases, consistent with numerical calculations.
  • Force measurements were independent of the distance between the optical trap and nanopore.
  • The force on dsRNA was found to be slightly lower than that on dsDNA.

Conclusions:

  • The nanopore-optical tweezers system is effective for probing dsRNA.
  • This technique expands possibilities for studying RNA structure, protein interactions, and molecular motor activity.
  • Potential applications include detecting RNA-bound proteins and analyzing RNA secondary structure.