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This Defense Intelligence Reference Document from the Defense Intelligence Agency, dated 10 December 2010, is one of a series of advanced technology reports produced in FY 2010 under the Advanced Aerospace Weapon System Applications (AAWSA) Program. It reviews quantum computing technologies and DNA-based molecular computing for onboard supercomputing on future spacecraft. It forecasts ion-trap quantum computers within 10 years, simple DNA tile computing within 20 years, and self-repairing DNA computers on a 40-year horizon.
“The Advance”7 pages
UNCLASSIFIED/ /F811. 8FFll!I.IIL 1!1!11!! 8HL"i' landscapes traversed by molecules. The capability for computation is also needed to analyze these data and, in many applications, some rudimentary processing units such as the logic gate networks shown in the previous section would be enough to achieve useful functionalities. To exhibit these capabilities, a team of scientists from Columbia University, Arizona State University, the University of Michigan, and the California Institute of Technology (Caltech) (123) have programmed an autonomous molecular "robot" made out of DNA to start, move, turn, and stop while following a DNA track. This development could ultimately lead to molecular systems that might one day be used for medical therapeutic devices and molecular-scale reconfigurable robots-robots made of many simple units that can reposition or even rebuild themselves to accomplish different tasks. The researchers constructed a trail of molecular "bread crumbs" on the DNA origami track by stringing additional single-stranded DNA molecules, or oligonucleotides, off the ends of the staples. These represent the cues that tell the molecular robots what to do-start, walk, turn left, turn right, or stop, for example-akin to the commands given to traditional robots. We will discuss the "nano walker" in greater detail in a later section in this treatise. It is this third function, the controlled movement of molecules through the aid of nanomotors that will be discussed next. DNA Nanomotors Molecular-size motors have evolved in nature, where they are used in virtually every important biological process. In contrast, the development of synthetic nanomotors that mimic the function of these amazing natural systems and that could be used in man-made nanodevices is in its infancy. Building nanoscale motors is not just an exercise in scaling down the design of a macroworld engine to nanoscale dimensions. Many factors such as friction, heat dissipation and many other mechanical behaviors are just very different at this scale - everything is constantly moving (under kinetic energy supplied by the heat of the surroundings) and being buffeted by other atoms and molecules (Brownian motion). The concept of a single DNA molecule nanomotor was already introduced in early 2002. (124) DNA nanomotors are synthetic biochemical devices whose motion can be controlled at the molecular scale. DNA molecular motors will be indispensable parts for the construction of molecular robots. The motion of a robot should be well-controlled by means of some molecular input, or it should be driven autonomously by cues from the environment. First approaches to encode molecular motion in DNA structures were based on the reversible and input-sensitive conformational changes. For example, the first reported use of a DNA motor was a nanomechanical device which generated twisting motion along the helix axis based on B-Z transition controlled by ionic strength of a solution. (125) Then, the first molecular tweezers were driven by successive reversible branch migrations of DNA strands, and these strands were called "fuel" and "anti-fuel." (126) The next level in complexity were "remotely- controlled" walkers introduced by Seeman and Pierce, as they were based on a series of successive unidirectional conformational changes driven by strand displacement. These sequential conformational changes were microscopic analogs of macroscopic commands such as: "lift the first leg", "drop the first leg to the next available position"; "lift the second leg", "drop the second leg to the next available position", with a cumulative result of a translational movement of a molecule along a track. One drawback of these systems was that they were not autonomous, and that each conformational change had to be triggered separately, while one advantage was that they could have been monitored easily in bulk with fluorescence measurements. The first autonomous systems were based on nucleic acid 41 UNCLASSIFIED// FOR OFFICIAL USE Gilt I
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Report, from the dia collection. The PDF is mirrored here; the original link is above. 54 pages are in the text index: search them above, or from the library's search.