Related Experiment Video
Updated: Sep 29, 2025

07:50
Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
Published on: November 25, 2015
14.5K
Dissipative Control over the Toehold-Mediated DNA Strand Displacement Reaction
Erica Del Grosso1, Patrick Irmisch2, Serena Gentile1
1Department of Chemistry, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133, Rome, Italy.
Angewandte Chemie (International Ed. in English)
|March 22, 2022
Summary
Researchers developed a new method for dissipative control in DNA nanotechnology. This approach re-engineers strand displacement reactions for controlled, reversible temporal activation of DNA systems.
Area of Science:
- Biochemistry
- Molecular Biology
- Nanotechnology
Background:
- Toehold-mediated strand displacement is a fundamental reaction in DNA nanotechnology.
- Current methods lack precise temporal control over reaction dynamics.
- Energy dynamics of strand displacement reactions are crucial for system design.
Purpose of the Study:
- To introduce a general approach for dissipative control over toehold-mediated strand displacement.
- To enable precise temporal activation and reversibility in DNA systems.
- To demonstrate novel applications in DNA structure labeling and cascade reactions.
Main Methods:
- Re-engineering the classic strand displacement reaction to incorporate energy dissipation.
- Converting high-energy invader strands into low-energy waste products.
- Utilizing energy-dissipating reactions to facilitate spontaneous system reset.
Main Results:
- Demonstrated dissipative control over toehold-mediated strand displacement.
- Achieved reversible control over the process for up to 10 cycles.
- Showcased high controllability and unique temporal activation capabilities.
Conclusions:
- The developed dissipative control strategy offers a powerful tool for DNA nanotechnology.
- This method enables transient labeling of DNA structures and temporal control of cascade reactions.
- The approach provides a general framework for designing dynamic and responsive DNA-based systems.
Related Concept Videos
Translesion DNA Polymerases
10.2K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
10.2K
DNA Topoisomerases
32.5K
Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
32.5K
Restarting Stalled Replication Forks
6.0K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
6.0K
Homologous Recombination
54.1K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
54.1K
The Replisome
35.4K
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
35.4K
DNA Helicases
22.5K
DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
22.5K

