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			by Kimberly Patch 
			
			TECHNOLOGY RESEARCH NEWS 
			
			March 28, 2005 
			
			from
			
			AllBusiness Website 
			
			  
			
			  
			
			  
			
				
					
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						Winfree's research 
						colleagues were Paul W. K. Rothemund and Nick 
						Papadakis. 
						
						  
						
						The work appeared in the 
						December, 2004 issue of Plos Biology. The research was 
						funded by the National Science Foundation (NSF), 
						the Defense Advanced Research Projects Agency (DARPA), 
						the National Aeronautics and Space Administration (NASA), 
						and GenTel. 
						 
						Please direct queries about this article to TRN at
						
						editor@trnmag.com (c) 
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			A decade after the idea became the topic 
			of his doctoral dissertation, a researcher at the California 
			Institute of Technology has showed that it is possible to coax short 
			strands of artificial DNA to spontaneously assemble into a 
			
			Sierpinski triangle. 
			 
			A Sierpinski triangle is a type of crystal, or structure that 
			regularly repeats. The Sierpinski triangle is
			
			fractal - a pattern of triangles 
			that looks the same in zoomed-in or zoomed-out views. The ability is 
			a step toward embedding programming instructions in chemical 
			processes.  
			
			  
			
			This is a corollary to the way computer 
			instructions are embedded in everything from automobile engines to 
			cell phones via microprocessors.  
			
				
				"Programmable embedded control makes 
				things possible that were virtually inconceivable," said Erik 
				Winfree, an assistant professor of computer science at The 
				California Institute of Technology. 
			 
			
			The DNA Sierpinski triangles show 
			that there is no theoretical barrier to using molecular 
			self-assembly to carry out any kind of computing and nanoscale 
			fabrication, according to Winfree.  
			
			  
			
			If someone comes up with the right 
			rules, the right set of molecules should be able to carry out the 
			instructions, he said.  
			
			 
			This type of algorithmic self-assembly is a testing ground for 
			learning how to embed logical rules within a molecular system so 
			that information processed by the molecules themselves is 
			responsible for directing the local processes, said Winfree. In the 
			case of a Sierpinski pattern, the molecules are directing the 
			process of self-assembly, he said. 
			 
			Although today's technology does not have electronics-like control 
			of chemical and molecular-scale processes, biology does.  
			
				
				"The only place one finds 
				sophisticated embedded control of chemical processes is in 
				biology, where biochemical information processing controls, 
				orchestrates [and] organizes all of life's functions." 
			 
			
			Algorithmic self-assembly can be thought 
			of as an extremely simplified version of organismal development, 
			said Winfree.  
			
			  
			
			Coaxing artificial strands of DNA to 
			form a Sierpinski pattern is,  
			
				
				"a far cry from an organism," he 
				said. "But it is also far more complex than the four DNA rule 
				tiles that directed its growth." 
			 
			
			DNA is made up of four bases - adenine, 
			cytosine, guanine and thymine - strung along a sugar-phosphate 
			backbone.  
			
			  
			
			Adenine and thymine, and
			cytosine and guanine can combine with each other. 
			Biological DNA forms the familiar double helix when a pair of single 
			strands that contain matching bases combine and coil up. Researchers 
			can make artificial strands form DNA tiles by engineering stretches 
			of one strand that match another strand.  
			
			 
			The researchers formed short strands of DNA capable of combining 
			into tiles that represent logic rules, short strands capable of 
			combining into tiles that represent input, and long nucleating 
			strands.  
			
			  
			
			They mixed the strands, heated the 
			solution, then let it cool slowly over several hours.  
			
				
				"At about 60 to 70 degrees Celsius, 
				the tiles spontaneously self-assemble from their components 
				strands, but it remains too hot for the tiles to associate with 
				each other," said Winfree. 
			 
			
			At the same or a slightly lower 
			temperature, the input tiles stick to the long nucleating strands.
			 
			
			  
			
			And somewhere between 30 and 40 degrees 
			Celsius the rule tiles begin to assemble onto the nucleating 
			structure to form, tile by tile, and layer by layer, the algorithmic 
			crystal.  
			
				
				"In some, few errors occur, and the 
				Sierpinski pattern emerges intact." 
			 
			
			The researchers have made Sierpinski 
			patterns on surfaces and more complicated Sierpinski triangles 
			in solution. Sierpinski triangles involve more types of 
			tiles. Some of the researchers' triangles were as large as one 
			micron, or thousandth of a millimeter. 
			 
			The keys to the researchers' success was using the long nucleating 
			DNA strands to get things started and a better microscope technique 
			to see what was happening. The errors were as interesting as the 
			successful Sierpinski patterns.  
			
			  
			
			The experiments' error rates ranged from 
			1 to 10 percent.  
			
				
				"We expected lots of errors, but we 
				didn't expect the kinds of errors that we saw," he said. 
				 
			 
			
			In general, several errors would 
			normally increase the randomness of a pattern.  
			  
			
			However, there were places within some 
			samples where several errors conspired to create large patches of 
			zero tiles or to perfectly terminate nascent Sierpinski triangles at 
			the corners, said Winfree.  
			
				
				"Such coincidences should be so rare 
				that one would never see a single instance in one million 
				crystals," he said. 
			 
			
			The researchers have a hypothesis 
			capable of explaining how these correlated errors arise,  
			
				
				"but it remains to be proven," said 
				Winfree. 
			 
			
			The researchers were also surprised to 
			see that one of the tile designs, instead of simply forming 
			two-dimensional sheets, formed a long tube with the sheets rolled 
			up. The DNA nanotubes are similar to but 10 times larger than
			
			carbon nanotubes, which are 
			rolled-up sheets of carbon atoms that form naturally in soot; they 
			are more similar to protein microtubules that self-assemble as part 
			of the cellular cytoskeleton. 
			 
			Carbon nanotubes can be narrower than a single nanometer, or 5,000 
			times narrower than a red blood cell. A nanometer is one millionth 
			of a millimeter. 
			 
			The researchers are working to decrease the method's error rate.
			 
			
				
				"We have developed some ideas for 
				how to embed error correction within the crystal growth process 
				- somewhat analogous to error-correcting codes in information 
				theory - and we are now trying to experimentally demonstrate 
				this scheme," said Winfree.  
			 
			
			If they are successful in reducing 
			assembly errors to insignificant levels,  
			
				
				"as the theory optimistically 
				predicts creating complex structures by self-assembly becomes a 
				form of programming," said Winfree. "If you can conceive of a 
				logical method for growing your structure, then it will work in 
				practice," he said. 
			 
			
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