I hope my liveblog of DNA 19 was amusing. There were a lot of great talks. People seemed to think mine was interesting. I have to say that Peng Yin and the members of his group stole the show a bit. DNA bricks and the superresolution microscopy were really beautiful, plus he is involved in the RNAi applications (with Niles Pierce and others) which are very exciting. I think that was absolutely incredible. But the nanopore was probably my favorite structure (from the Simmel lab). All in all, I learned a lot and was very grateful to participate.

Kurt Gothelf showed how DNA can be used to assemble polymers. I usually think of polymerization reactions as being very random. I thought it was interesting that he can define a path across the surface of a DNA origami tile to make a directed polymer chain. The shape and structure are both controlled. These polymers also bind carbon nanotubes, so now you can put carbon nanotuves along defined paths? That sounds promising.

Tim Liedl talked about engineering metamaterials with DNA. Metamaterials have behavior that depends on their structure rather than their composition. Gold nanoparticles are very different than solid gold. They are arranging the gold/metal nanoparticles by using DNA. I lost the thread of the novelty of this material. I do remember when this group published a paper using gold nanoparticle-decorated DNA to control the chirality and optical activity of structures. They could make the little spiral gold structures rotate polarized light left or right depending on how they assembled it.

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Friedrich Simmel showed recent work in functional nanochannels produced using hydrophobically-modified DNA. They are big and leaky but they work! They insert themselves into a membrane and make a big channel. Simmel also talked about hydrophobic folding of origami. That is really interesting from a protein folding perspective. It is not programmable like base-pairing, but it is orthogonal to base pairing and might be versatile in other contextx. They also made droplets and put a chemical reaction network oscillator inside. Evidently, sometimes, small droplets can oscillate but not larger ones. I would like to explore why that is in more detail. It certainly looks great.

Ned Seeman. Everyone in the field knows Ned Seeman’s contribution. The great vision was to use hexamer scaffolds extending in wide, repeating units to stabilize other crystals. He put the kibosh on that. It turns out that almost everything you might include in such a network destabilized it. But it did end up working and it did make some neat structures. Really, the Seeman group pioneered the structural DNA design idea. He also talked about Alex Rich in 1956 inventing hybridization, of which I had no prior knowledge.

John Spence talked about how X-ray lasers can be used for structural and dynamic biology. The system takes destructive snapshots and averages them (since each snapshot uses so much X-ray radiation that the molecules are destroyed in the process). Nonetheless, this can build up an average picture. If you do pulse-delay experiments, you can get a time-resolved movie of a molecular process. Very cool.