Related Experiment Video
Updated: May 20, 2026

09:43
Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores
Published on: October 31, 2013
Assessing graphene nanopores for sequencing DNA
David B Wells1, Maxim Belkin, Jeffrey Comer
1Department of Physics, University of Illinois, 1110 W. Green St., Urbana, Illinois 61801, USA.
Nano Letters
|July 12, 2012
Summary
Simulations show single-stranded DNA can move through graphene nanopores one nucleotide at a time. Controlling nucleotide orientation may enable DNA sequencing via ionic current blockades.
Area of Science:
- Nanotechnology
- Biophysics
- Computational Biology
Background:
- Graphene nanopores offer potential for DNA analysis.
- Understanding DNA translocation dynamics is crucial for sequencing technologies.
Purpose of the Study:
- To simulate and characterize single-stranded DNA translocation through graphene nanopores.
- To investigate ionic current blockades generated by DNA nucleotides.
- To assess the feasibility of DNA sequencing using graphene nanopores.
Main Methods:
- All-atom molecular dynamics simulations.
- Atomic-resolution Brownian dynamics simulations.
- Analysis of ionic current blockades.
Main Results:
- DNA translocation can occur in discrete, single-nucleotide steps.
- Hydrophobic interactions reduce nucleotide conformational fluctuations.
- Ionic current blockades are nucleotide-type dependent but sensitive to orientation.
Conclusions:
- DNA sequencing using graphene nanopores is potentially feasible.
- Precise engineering of nanopore surfaces is key to controlling DNA conformation.
- This approach could advance rapid DNA analysis techniques.
Related Concept Videos
Sanger Sequencing
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
Next-generation Sequencing
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.

