Related Experiment Video
Updated: Aug 3, 2026

13:32
Designing a Bio-responsive Robot from DNA Origami
Published on: July 8, 2013
22.4K
Modulating transformation of DNA origami nanoarray via sequence design
Dongfang Wang1,2, Fiona Cole3, Martina Pfeiffer3
1School of Biomedical Engineering, University of Science and Technology of China, Hefei, China.
Nature Communications
|July 2, 2025
Summary
Researchers explored DNA domino arrays, finding that base design at four-way junctions controls nanoarray transformations. This work enables predictable modulation of DNA nanostructures for advanced applications.
Area of Science:
- DNA nanotechnology
- Structural DNA nanotechnology
- Biomolecular engineering
Background:
- Four-way DNA junctions are fundamental building blocks in DNA nanotechnology.
- Reconfigurable DNA nanoarrays (domino arrays) utilize these junctions for stepwise transformations.
- Understanding junction design is crucial for controlling nanoarray behavior.
Purpose of the Study:
- To investigate how DNA base design at four-way junctions influences the kinetics and thermodynamics of transformations in DNA domino arrays.
- To establish a platform for studying the designable modulation of DNA nanoarray transformations.
- To explore the coordinated transformation of multiple four-way junctions within a nanoarray.
Main Methods:
- Fabrication of a DNA domino array with uniform sequences at each junction.
- Utilizing Atomic Force Microscopy (AFM) for structural imaging.
- Employing single-molecule Förster resonance energy transfer (smFRET) microscopy for kinetic and thermodynamic analysis.
Main Results:
- Demonstrated that specific DNA base designs at junctions enable predictable modulation of four-way junction configurations.
- Showcased the ability to regulate the energy difference between junction states, controlling transformation pathways.
- Observed coordinated transformations across the DNA domino array.
Conclusions:
- The design of DNA bases at four-way junctions is a key factor in controlling the transformation dynamics of reconfigurable DNA nanoarrays.
- This study provides a foundation for the rational design of complex, stepwise transformations in DNA nanostructures.
- The developed platform facilitates detailed investigation of nanoarray behavior using advanced microscopy techniques.
Related Concept Videos
Gene Conversion
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Conservative Site-specific Recombination and Phase Variation
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
DNA Microarrays
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
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...
Maxam-Gilbert Sequencing
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Challenges of the Maxam-Gilbert Method
The...
Gene Conversion
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...

