Crowdsurfing motor proteins create possible prosthetic interface.
Using a succession of biological mechanisms, Sandia National Laboratories researchers have created linkages of polymer nanotubes that resemble the structure of a nerve, with many out-thrust filaments poised to gather or send electrical impulses.
“This is the first demonstration of naturally occurring proteins assembling chemically created polymers into complex structures that modern machinery can’t duplicate,” said Sandia National Laboratories researcher George Bachand.
Sandia co-researcher Wally Paxton said, “This is foundational science, but one possibility we see, way down the road, is to use soft artificial structures like these to painlessly interface with the body’s nerve structures.”
Currently, rigid electrodes that cause inflammation are used to penetrate nerve tissue trying to communicate with an artificial limb, he explained. Instead, in a future application, the polymer network could be used extend the nerve, providing a gentler prosthetic interface.
Proteins like Disney’s enchanted brooms
Creation of the neural structure, unachievable by normal manufacturing techniques, begins by altering the behavior of kinesin motor proteins — biological machines found in every human cell. These tiny motors normally tote material from one part of a cell to another, carrying them on what, in video graphics, is portrayed as a vertical body with two legs. These stride along protein microtubules that form the cell structure. The purposefulness of the motors resembles that of the spellbound brooms in Disney’s Fantasia, relentlessly carrying buckets of water up the castle stairs.
Turning natures’ machinery on its head, the researchers used known techniques to glue the “shoulders” of kinesin motors to a glass substrate. This prevents their bodies from travelling, but their “legs” above them continue their vigorous movements. These pass microtubules above them, like an audience crowdsurfing entertainers on upraised hands.
In the next laboratory step, these travelling protein microtubules, microns in length, encounter relatively large polymer spheres, tens of microns in diameter, inserted by the researchers.
“At that point, we have structures that want to do work — the kinesin-powered microtubules — and something they want to do work on — the spheres,” Paxton said.
The microtubules, pre-coated with a sticky substance, pinch off polymer nanotubes from the sphere that lengthen as the kinesin motors travel on. The process resembles stringy strands of cheese lengthening as a piece of pizza is removed from a pan, said Paxton.
As the nanotubes lengthen and crosslink, they form structures complex enough to bring to mind the lights of a city seen at night from an airplane at high altitude. The networks range from hundreds of micrometers to tens of millimeters in total size and are composed of tubes 30 to 50 nanometers in diameter.
“One goal of our work is to make an artificial, highly branched neural structure,” said Bachand. “The next step is, can we wire them together? The answer is, the motors should do it naturally. And two such networks, joined together, would have self-healing built into them. The motors never stop running until they run out of fuel. A neural branch breaks, and then a motor can act on that area to produce a new branch.”
The insertion of quantum dots also proved stable, which means that light could be used to carry information through the structure as well as electricity.
Funding: The work is supported by the Department of Energy’s Office of Basic Energy Sciences, and performed in part at its Center for Integrated Nanotechnologies, an Office of Science user facility.
Source: Neal Singer – Sandia National Laboratories
Image Source: The images are credited to Sandia National Laboratories
Original Research: Abstract for “Dynamic assembly of polymer nanotube networks via kinesin powered microtubule filaments” by Walter F. Paxton, Nathan F. Bouxsein, Ian M. Henderson, Andrew Gomez, and George D. Bachand in Nanoscale. Published online April 24 2015 doi:10.1039/C5NR00826C
Abstract
Dynamic assembly of polymer nanotube networks via kinesin powered microtubule filaments
We describe for the first time how biological nanomotors may be used to actively self-assemble mesoscale networks composed of diblock copolymer nanotubes. The collective force generated by multiple kinesin nanomotors acting on a microtubule filament is large enough to overcome the energy barrier required to extract nanotubes from polymer vesicles comprised of poly(ethylene oxide-b-butadiene) in spite of the higher force requirements relative to extracting nanotubes from lipid vesicles. Nevertheless, large-scale polymer networks were dynamically assembled by the motors. These networks displayed enhanced robustness, persisting more than 24 h post-assembly (compared to 4–5 h for corresponding lipid networks). The transport of materials in and on the polymer membranes differs substantially from the transport on analogous lipid networks. Specifically, our data suggest that polymer mobility in nanotubular structures is considerably different from planar or 3D structures, and is stunted by 1D confinement of the polymer subunits. Moreover, quantum dots adsorbed onto polymer nanotubes are completely immobile, which is related to this 1D confinement effect and is in stark contrast to the highly fluid transport observed on lipid tubules.
“Dynamic assembly of polymer nanotube networks via kinesin powered microtubule filaments” by Walter F. Paxton, Nathan F. Bouxsein, Ian M. Henderson, Andrew Gomez, and George D. Bachand in Nanoscale. Published online April 24 2015 doi:10.1039/C5NR00826C
