Related Experiment Video
Updated: Apr 19, 2026

13:32
Designing a Bio-responsive Robot from DNA Origami
Published on: July 8, 2013
23.0K
Programmable motion of DNA origami mechanisms
Alexander E Marras1, Lifeng Zhou1, Hai-Jun Su1
1Department of Mechanical and Aerospace Engineering, The Ohio State University, Columbus, OH 43210.
Summary
Researchers engineered DNA origami machines with tunable joints for precise nanoscale motion. These DNA machines exhibit complex, reversible movements, paving the way for advanced nanorobotics.
Area of Science:
- Nanotechnology
- Molecular Engineering
- Biophysics
Background:
- DNA origami allows for the creation of nanoscale structures with high precision.
- Engineering dynamic and movable nanoscale components remains a significant challenge.
Purpose of the Study:
- To develop and demonstrate complex, reversible motion in DNA origami machine elements.
- To integrate simple DNA joints into sophisticated 2D and 3D mechanisms.
- To actuate these DNA mechanisms using input strands for programmable conformational changes.
Main Methods:
- Designing and fabricating flexible DNA origami rotational and linear joints with tunable stiffness and motion range.
- Integrating single-degree-of-freedom joints into higher-order mechanisms like crank-sliders and Bennett linkages.
- Utilizing DNA input strands for distributed actuation to control reversible structural transformations.
Main Results:
- Demonstrated mechanical behavior of DNA origami joints with constrained motion along a single degree of freedom.
- Successfully built and characterized 2D (crank-slider) and 3D (Bennett linkage) DNA origami mechanisms.
- Achieved reversible conformational changes of the entire DNA structure on minute timescales via distributed actuation.
Conclusions:
- Programmable motion of 2D and 3D DNA origami mechanisms can be achieved.
- A macroscopic machine design approach is effective for constructing complex DNA origami systems.
- This work advances the development of DNA-based nanomachines with controlled dynamic behavior.
Related Concept Videos
The Replisome
39.9K
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...
39.9K
DNA Helicases
25.3K
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...
25.3K
The DNA Replication Fork
43.6K
An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork. Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication...
43.6K
Nucleosome Remodeling
11.7K
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
11.7K
DNA Topoisomerases
38.4K
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. ...
38.4K
Lagging Strand Synthesis
64.5K
During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
64.5K

