‘Nano-camo’ for fashionistas and environmentalists
ALBUQUERQUE, N.M. — Certain fish species blend with their environment by changing color.
Sandia National Laboratories researchers have demonstrated that, in theory, they could cause synthetic materials to change color like fish do.
“Camouflage outfits that blend with a variety of environments without need of an outside power source — say, blue when at sea and then brown in a desert environment — is where this work could eventually lead,” says principal investigator George Bachand. “Or the same effect could be used in fabricating chic civilian clothing that automatically changes color to fit different visual settings.”
Such clothing could be a reality in five to ten years, he says.
The power source for both the biological and the lab method relies on the basic cellular fuel called ATP, which releases energy as it breaks down. Fifty percent (roughly) is absorbed by the motor proteins — tiny molecular motors able to move along surfaces.
When fish change colors, motor proteins aggregate and disperse skin pigment crystals carried in their “tails” as they walk with their “feet” along the microtubule skeleton of the cell. By this means, they rearrange the color display.
Introducing an on/off switch
To put motor proteins in motion or switch them off, nature uses complex signaling networks. The Bachand group’s method is simpler. It involves the simple genetic insertion of a kind of docking port in the motor protein’s structure. What docks are zinc ions. Bound zinc ions turn the protein’s action to “off.” Stripping zinc ions out with chemical agents allows the motor protein to work again. The effect is controllable, and even reversible.
“We essentially reengineered the protein structure to introduce a switch into the motor,” says Bachand. “So we can now turn our nanofluidic devices on and off.”
Previous efforts at regulating motor activity have used fuel intake as a control mechanism: the less the fuel, the slower the process. The Bachand group’s switch, operated independently of fuel changes, resembles the improvement in early automobile technologies when a simple ignition switch took over for more complicated rheostats. The paper describing this work was a spotlighted article in the journal Biotechnology and Bioengineering (vol. 100, p. 478).
But what is it that the switch operates?
In a cover article in the high-profile journal Advanced Materials (Dec. 2, 2008), the Sandia team describes a kind of inverted cellular world, where motor proteins do not run about but instead are upended so that their tails are embedded in a protein-modified layer on a glass slide. Free-ranging microtubules — cylindrical protein filaments — instead of forming the cellular skeleton of cells, are passed along by the waving feet of the motor proteins like crowd surfers at a rock concert, or like buckets passed hand-to-hand along a line of firefighters.
The traveling microtubules are coated with quantum dots — nanoscopic groups of atoms that emit light, their frequency dependent on dot size.
The dots emit different frequency of light than they adsorb, while the biological system merely reflects incoming wavelengths. But they perform similar coloring functions.
The telephone cord twist
When motor-transported microtubules collide, the microtubules stick together and twist until they resemble a desk phone cord. The twisting process ultimately forces the formation of stable rings approximately five micrometers in diameter. Their docked quantum dots (cadmium selenide) produce a range of light frequencies.
When mechanical strain in the rings causes them to rupture, the cracked segments are tugged out by the nearby motors until the ring is completely disassembled. The formation and destruction of the two states — free microtubules and rings — can be reversibly controlled.
Thus the dots can be tightly packed or dispersed — optically, an essential ingredient in the perception of color change.
The process resembles the action of fish color changes, which require one group of motor proteins carrying pigments to be “on” all the time while a second group of motor proteins is turned on by complex biological processes at the right time. This produces a tug-of-war between motor groups that results in pigment dispersion and ultimately a color change. When the second motor is switched off, the color returns to the ground aggregate state.
“Our overall process mimics the fish,” says Bachand. “We essentially go from a dispersed particle state to a concentrated one and then back again to dispersed, similar to the fish. Thus, in principle, the mechanism could produce a color change. The underlying science provides a new basis for materials scientists to begin working toward real-world applications.”
The work was supported by DOE Basic Energy Sciences and Sandia’s Laboratory Directed Research & Development office.
Key contributors to the Biotechnology & Bioengineering paper were Adrienne Greene and Amanda Trent (now a graduate student at University of California, Santa Barbara). Advanced Materials paper contributors were Haiqing Liu (now at Los Alamos National Laboratory), Erik Spoerke, Marlene Bachand, Steve Koch (former Sandia employee, now an assistant professor at the University of New Mexico), and Bruce Bunker.
Sandia is a multiprogram laboratory operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin, for the U.S. Department of Energy’s National Nuclear Security Administration. With main facilities in Albuquerque, N.M., and Livermore, Calif., Sandia has major R&D responsibilities in national security, energy and environmental technologies, and economic competitiveness.
Sandia news media contact: Neal Singer, email@example.com