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Breakthrough in controlling DNA-based robots



Assembly of systems @ Ohio State University

Researchers have devised a magnetic control system to make tiny DNA-based robots move on demand—and much faster than recently possible.

In the journal Nature Communications, Carlos Castro and Ratnasingham Sooryakumar and their colleagues from The Ohio State University report that the control system reduced the response time of prototype nano-robot components from several minutes to less than a second.

Not only does the discovery represent a significant improvement in speed, this work and one other recent study herald the first direct, real-time control of DNA-based molecular machines.

The discovery could one day enable nano-robots to manufacture objects – such as drug-delivery devices -- as quickly and reliably as their full-size counterparts. Previously, researchers could only move DNA indirectly, by inducing chemical reactions to coax it to move certain ways, or introducing molecules that reconfigure the DNA by binding with it. Those processes take time.

“Imagine telling a robot in a factory to do something and having to wait five minutes for it to perform a single step of a task. That was the case with earlier methods for controlling DNA nano-machines,” said Castro, associate professor of mechanical and aerospace engineering.

“Real-time manipulation methods like our magnetic approach enable the possibility for scientists to interact with DNA nano-devices, and in turn interact with molecules and molecular systems that could be coupled to those nano-devices in real-time with direct visual feedback.”

In earlier work, Castro’s team used a technique called DNA origami to fold individual strands of DNA to form simple microscopic tools like rotors and hinges. They even built a “Trojan horse” out of DNA for delivering drugs to cancer cells.

For this new study, the researchers joined with Ratnasingham Sooryakumar, professor of physics. He previously developed microscopic magnetic “tweezers” for moving biological cells in biomedical applications such as gene therapy. The tweezers were actually made of groups of magnetic particles that moved in sync to nudge the cells where people wanted them to go.

Those magnetic particles, while invisible to the naked eye, were still many times bigger than one of Castro’s nano-machines, Sooryakumar explained.

“We had discovered a way to harness the power of magnetic forces to probe the microscopic world—a hidden world of astounding complexity,” he said. “But we wanted to transition from the micro-world to the nano-world. This led to the collaboration with Dr. Castro. The challenges were to shrink the functionality of our particles a thousand-fold, couple them to precise locations on the moving parts of the machines and incorporate fluorescent molecules as beacons to monitor the machines as they moved.”

For this study, the team built rods, rotors and hinges using DNA origami. Then they used stiff DNA levers to connect the nanoscopic components to miniature beads made from polystyrene impregnated with magnetic material. By adjusting a magnetic field, they found they could command the particles to swing components back and forth or rotate them. The components executed the instructed movements in less than a second.

For example, the nano-rotor was able to spin a full 360 degrees in about one second with continuously controlled motion driven by a rotating magnetic field. The nano-hinge was able to be closed or opened in 0.4 seconds, or held at a specific angle with a precision of 8 degrees.

These movements could have taken several minutes if executed with traditional methods, Castro said. He envisions that complex nano-materials or biomolecular complexes could one day be fabricated in DNA-based nano-factories that detect and respond to their local environment.

Real-time magnetic actuation of DNA nanodevices via modular integration with stiff micro-levers Stephanie Lauback, Kara R. Mattioli, Alexander E. Marras, Maxim Armstrong, Thomas P. Rudibaugh, Ratnasingham Sooryakumar & Carlos E. Castro Nature Communications Volume 9, Article number: 1446 (2018)

Ohio State University

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