Researchers in Denmark and Germany have used an origami technique to make a nanometre-sized box with a lid that can be locked and unlocked. The box is made of DNA and measures 42 × 36 × 36 nm, which means that it can easily carry various kinds of tiny cargo such as a single virion or ribosome. It might be used as a container for drug delivery or as a new type of biosensor, say the scientists.
The DNA box is the largest and most complex artificial self-assembled structure reported to date, explains Jorgen Kjems of Aarhus University. It is also the smallest box ever made.
The DNA origami method was developed in the US by Paul Rothemund at Caltech in 2006 and was originally used to construct 2D DNA structures. Origami is the Japanese word for paper folding — and the DNA technique involves folding a large single-stranded DNA genome into a sheet. This is done by adding more than 200 small synthetic DNA sequences called “staple strands”.
Kjems and colleagues have now extended this technique by developing software that can fold any 2D nanostructure, and recently also 3D structures such as their nano-box.
The DNA origami method was developed in the US by Paul Rothemund at Caltech in 2006 and was originally used to construct 2D DNA structures. Origami is the Japanese word for paper folding — and the DNA technique involves folding a large single-stranded DNA genome into a sheet. This is done by adding more than 200 small synthetic DNA sequences called “staple strands”.
Kjems and colleagues have now extended this technique by developing software that can fold any 2D nanostructure, and recently also 3D structures such as their nano-box.
Enough room for a ribosome:
The box is large enough to hold a single ribosome or poliovirus and its six faces are formed from parallel, interlinked DNA helices folded into shape thanks to 220 short synthetic nucleus strands (or oligonucleotides).
The lid of the box closes when two DNA sequences in the lid recognize two complementary sequences inside the box. The two DNA helices that subsequently form close the box.
However, something else can happen too: two specific external RNA or DNA sequences can form longer helices with the two DNA locks inside the box. These two external sequences "out compete" the helices inside the locks and release the lid. "The lid will then automatically open thanks to repulsion between all of the negative charges in the box," Kjems said.
The lid of the box closes when two DNA sequences in the lid recognize two complementary sequences inside the box. The two DNA helices that subsequently form close the box.
However, something else can happen too: two specific external RNA or DNA sequences can form longer helices with the two DNA locks inside the box. These two external sequences "out compete" the helices inside the locks and release the lid. "The lid will then automatically open thanks to repulsion between all of the negative charges in the box," Kjems said.
New type of sensor:
As well as being able to carry and deliver drugs inside cells, the box might also act as an amplifier. This is because the presence of only two DNA molecules can lead to the release of a large number of reporter compounds inside the box, says Kjems. It could thus be used to develop a new type of biosensor. The team, which includes researchers from the Max Planck Institute for Biological Chemistry and the University of Göttingen, both in Germany, will now test drug delivery inside cells using the nano-box.
The work was reported in Nature.
The work was reported in Nature.
About the author:
Belle Dumé is a contributing editor to nanotechweb.org
Belle Dumé is a contributing editor to nanotechweb.org
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