DNA ‘origami’ could help build faster, cheaper computer chips
SAN DIEGO, March 13, 2016 — Electronics manufacturers constantly hunt for ways to make faster, cheaper computer chips, often by cutting production costs or by shrinking component sizes. Now, researchers report that DNA, the genetic material of life, might help accomplish this goal when it is formed into specific shapes through a process reminiscent of the ancient art of paper folding.
The researchers present their work today at the 251st National Meeting & Exposition of the American Chemical Society (ACS). ACS, the world's largest scientific society, is holding the meeting here through Thursday. It features more than 12,500 presentations on a wide range of science topics.
"We would like to use DNA's very small size, base-pairing capabilities and ability to self-assemble, and direct it to make nanoscale structures that could be used for electronics," Adam T. Woolley, Ph.D., says. He explains that the smallest features on chips currently produced by electronics manufacturers are 14 nanometers wide. That's more than 10 times larger than the diameter of single-stranded DNA, meaning that this genetic material could form the basis for smaller-scale chips.
"The problem, however, is that DNA does not conduct electricity very well," he says. "So we use the DNA as a scaffold and then assemble other materials on the DNA to form electronics."
To design computer chips similar in function to those that Silicon Valley churns out, Woolley, in collaboration with Robert C. Davis, Ph.D., and John N. Harb, Ph.D., at Brigham Young University, is building on other groups' prior work on DNA origami and DNA nanofabrication.
The most familiar form of DNA is a double helix, which consists of two single strands of DNA. Complementary bases on each strand pair up to connect the two strands, much like rungs on a twisted ladder. But to create a DNA origami structure, researchers begin with a long single strand of DNA. The strand is flexible and floppy, somewhat like a shoelace. Scientists then mix it with many other short strands of DNA — known as "staples" — that use base pairing to pull together and crosslink multiple, specific segments of the long strand to form a desired shape.
However, Woolley's team isn't content with merely replicating the flat shapes typically used in traditional two-dimensional circuits. "With two dimensions, you are limited in the density of components you can place on a chip," Woolley explains. "If you can access the third dimension, you can pack in a lot more components."
Kenneth Lee, an undergraduate who works with Woolley, has built a 3-D, tube-shaped DNA origami structure that sticks up like a smokestack from substrates, such as silicon, that will form the bottom layer of their chip. Lee has been experimenting with attaching additional short strands of DNA to fasten other components such as nano-sized gold particles at specific sites on the inside of the tube. The researchers' ultimate goal is to place such tubes, and other DNA origami structures, at particular sites on the substrate. The team would also link the structures' gold nanoparticles with semiconductor nanowires to form a circuit. In essence, the DNA structures serve as girders on which to build an integrated circuit.
Lee is currently testing the characteristics of the tubular DNA. He plans to attach additional components inside the tube, with the eventual aim of forming a semiconductor.
Woolley notes that a conventional chip fabrication facility costs more than $1 billion, in part because the equipment necessary to achieve the minuscule dimensions of chip components is expensive and because the multi-step manufacturing process requires hundreds of instruments. In contrast, a facility that harnesses DNA's knack for self-assembly would likely entail much lower start-up funding, he states. "Nature works on a large scale, and it is really good at assembling things reliably and efficiently," he says. "If that could be applied in making circuits for computers, there's potential for huge cost savings."
A press conference on this topic will be held Monday, March 14, at 1 p.m. Pacific time in the San Diego Convention Center. Reporters may check-in at Room 16B (Mezzanine) in person, or watch live on YouTube http://bit.ly/ACSliveSanDiego. To ask questions online, sign in with a Google account.
The researchers acknowledge funding from the Semiconductor Research Corporation.
The American Chemical Society is a nonprofit organization chartered by the U.S. Congress. With more than 158,000 members, ACS is the world's largest scientific society and a global leader in providing access to chemistry-related research through its multiple databases, peer-reviewed journals and scientific conferences. Its main offices are in Washington, D.C., and Columbus, Ohio.
To automatically receive news releases from the American Chemical Society, contact [email protected]
Note to journalists: Please report that this research is being presented at a meeting of the American Chemical Society.
Follow us: Twitter | Facebook
3D DNA Origami Templated Nanoscale Device Fabrication
Because electronic and mechanical devices continue to decrease in size, exploring nontraditional fabrication methods provides added opportunities. For example, materials not currently used in devices, such as biological molecules, can contribute to new fabrication procedures. Self-assembling biological molecules especially show promise as useful starting materials, because nanodevice fabrication can exploit interactions that lead to highly specific self-assembly. DNA origami is a method that folds pieces of single-stranded DNA into designed structures by taking advantage of nucleotide base-pairing. Designs that include single-stranded extensions can provide further attachment points for other materials such as metal nanoparticles and nanorods. Such specific placement of metal on a DNA origami template can create nanowires as part of a larger nanocircuit. 2-D DNA origami templates can help position materials in a planar circuit pattern, but 3-D DNA origami uses a third dimension to further compact the nanocircuit elements. To test possible applications of 3-D origami, I designed a tube-shaped DNA origami with a hollow center. To verify correct folding of DNA origami structures, I stained them with lanthanum (III) and lead (II) and imaged them with SEM. I also made two variations of the tube-shaped origami, one with a location for nanoparticle attachment at an end of the tube and one with a location for particle attachment in the center of the tube. To verify successful attachment of gold nanoparticles, I confirmed with SEM imaging the presence of origami-nanoparticle hybrids. This design provides several possibilities for attachment of nanomaterials, both inside the hollow center and to the outside of the tube, which provide a pathway to creating a vertical nanowire logic gate. A flat base-like DNA origami could then position an array of tube DNA origami structures for more complex applications. An array of this type could be a step towards making more compact electronics.
619-525-6215 (San Diego Press Center, March 13-16)
202-872-6042 (D.C. Office)
Katie Cottingham, Ph.D.