
The Biodesign Institute Arizona State University
Figure 1 a and b display schematics for 2-D nanoforms with accompanying AFM images of the resulting structures. 1 c-e represent 3D structures of hemisphere, sphere and ellipsoid, respectively, while figure 1f shows a nanoflask, (each of the structures visualized with TEM imaging).
Earlier this week, we learned about wedding rings made out of DNA. Now, the ability to fold stringy bits of DNA into patterns and shapes has gone 3-D thanks to a new technique pioneered at Arizona State University's Biodesign Institute.
The breakthrough, reported in the April 15 issue of Science, is a step on the road to eventually using the procedure to create diminutive drug delivery devices, nano-computers, and chemical factories.
So-called DNA origami was introduced in 2006 by Paul Rothemund of the California Institute of Technology. It hinges on the self-assembling properties of DNA's four complimentary base pairs, which form the famous double helix.
These nucleotides, labeled A, T, C and G, follow a formula of how they interact. A always pairs with T and C with G. DNA origami practitioners exploit this base pairing to create complex shapes, but until now most shapes were two dimensional.
To do this, they frame the desired shape with a length of single-stranded DNA and then use DNA "staple strands" to cross over and integrate the structure and hold the desired shape.
"Our goal is to develop design principles that will allow researchers to model arbitrary 3-D shapes with control over the degree of surface curvature," Yan Liu of the Biodesign Institute, said in a news release explaining the research.
"In an escape from a rigid lattice model, our versatile strategy begins by defining the desired surface features of a target object with the scaffold, followed by manipulation of DNA conformation and shaping of crossover networks to achieve the design."
To achieve this, the team starts with simple, 2-D concentric ring structures formed from a DNA double helix and bound together at strategically placed crossover points. Varying the number of nucleotides between crossover points allows the designer to combine sharp and rounded elements into 2-D and 3-D forms.
More on tricks with DNA:
- 'Wedding Rings' made out of DNA
- Slideshow: Making smiley faces from DNA
- DNA robots pave way for microscopic factories
- DNA twisted into pretzels
- Play a game and engineer real RNA
John Roach is a contributing writer for msnbc.com. Connect with the Cosmic Log community by hitting the "like" button on the Cosmic Log Facebook pageor following msnbc.com's science editor, Alan Boyle, on Twitter (@b0yle).


Just as long as we don't accidentally, or on purpose, create a virus like pathogen.
That's MUCH more likley to happen in the millions of pharmaceutical research labs than in the folding of DNA.
Randi, there aren't millions of pharmaceutical labs, and those that do exist aren't trying to breed new organisms.
There are a few Biological Warfare labs, but they mostly research means of defense. Why? Because every analysis of the use of biological warfare has shown the inevitability of the agent mutating into a new pathogen that bypasses the vaccine given to their own people. Both sides would be devastated.
Regardless, folding dna doesn't make new pathogens it just changes the angles of the dna double helix. Any place that houses/tests/manipulates pathogens has a higher potential of harboring drug resistant strains.
http://www.msnbc.msn.com/id/42611389/
Randi, I hope you are correct. There is an old definition of exploration and science in general; It is the process of finding new and unusual ways to get killed. ;-p