Ten years after its introduction, DNA origami, a fast and simple way to assemble DNA into potentially useful structures, is finally coming into its own.
In a recent paper in Journal of the American Chemical Society, a team of researchers used the technique to program DNA to form large, two-dimensional honeycombs and tubes. Because those structures are assembled biologically, rather than by conventional chemical reactions, they have very precise and repeatable structures. The researchers programmed those structures to hold gold nanoparticles in arrangements that gave them unusual optical properties.
This is just one of many potential applications for DNA origami, which uses short, easily synthesized strands of DNA to "staple" long DNA strands into complex structures.
In a roundtable, The Kavli Foundation brought together three pioneers in the field to discuss the technique's potential. They included one of the paper's co-authors, William Shih, an associate professor of Biological Chemistry and Molecular Pharmacology at Harvard Medical School and Cancer Biology at the Dana-Farber Cancer Institute.
In addition to using DNA origami to create electronic devices, Shih is interested in using it to make new types of medicines. Existing drugs, he notes, are usually small molecules that "gum up the works of some process." Instead, he envisions exposing the immune system to DNA origami scaffolds that are holding pieces of virus. These complexes would "teach" the body to recognize the virus and develop antibodies to it before a live virus attacks.
"If we want to rival the immune system in effectiveness, we must rival it in complexity," Shih said in the roundtable discussion.
Other medicines might take advantage of the arrangement of proteins on cell surfaces, added Paul Rothemund, who received a MacArthur Fellowship for inventing DNA origami 10 years ago, and was one of the three participants. He is a research professor and faculty member at the Kavli Nanoscience Institute at the California Institute of Technology.
Antibodies, Rothemund argued, bind with invading molecules in atomically precise ways to neutralize them. Many researchers believe large-scale patterns of proteins on antibody surfaces control this behavior.
"DNA origami could allow us to arrange proteins in ways that give us access to the language of the immune system. This might make very sophisticated medicines possible," said Rothemund.
Rothemund also sees potential for DNA origami semiconductors. Chemists already know how to synthesize single molecules that act like transistors or diodes. DNA origami could give them a way to organize those molecules into larger systems where they could interact with one another to perform computations.
"Paul [Rothemund] and I often try to compare computing with our field, which, if you think about it, involves programming biomolecules to self-assemble into whatever we want," said Shawn Douglas, an assistant professor of Cellular & Molecular Pharmacology in the University of California, San Francisco, School of Medicine. "We believe programmed biomolecules are going to be just as transformative."
One of Douglas' research interests is immobilizing proteins in DNA origami cages in order to take X-ray portraits of them. This would free chemists from having to crystallize proteins, a process that is time-consuming and often fails, to understand their structure.
Douglas is also helping to move DNA programming forward in other ways. He developed caDNAno software, which enables researchers to design complex DNA origami structures. He also leads BIOMOD, an international biomolecular design competition for college students.
"If we can build out the biology the way we built out electronics, we can create all these amazing and useful things," Douglas said.
Rothemund agreed: For a long time, he says, scientists treated nature's designs as sacred, and believed that we could never fruitfully modify them.
"Today, there is a new spirit about engineering these systems, and we have tools that make these modifications easier than ever" he said. "So instead of merely studying a system, 20-year-olds are saying, 'Let's do something to make it more useful.'"
More information: Pengfei Wang et al, Programming Self-Assembly of DNA Origami Honeycomb Two-Dimensional Lattices and Plasmonic Metamaterials, Journal of the American Chemical Society (2016). DOI: 10.1021/jacs.6b03966
Journal information: Journal of the American Chemical Society
Provided by The Kavli Foundation