NANO: Controlling Errors in Algorithmic Self-Assembly: Characterization, Modeling, and Implementation
NANO: Controlling Errors in Algorithmic Self-Assembly: Characterization, Modeling, and Implementation
批准号:
0432193
负责人:
Erik Winfree
金额:
$30.0万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-08-15 至 2007-07-31
中文摘要
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英文摘要
Biological organisms are self-organized chemical systems that carry out algorithms encoded in the geneticmaterial, DNA. Biology thus provides clear proof that autonomous chemical systems can be programmed tocompute. The ability to program biomolecular systems that control chemical fabrication and informationprocessing tasks would result in a dramatic increase in the level of sophistication in bionanotechnology.The Winfree laboratory has been developing programmable biomolecular systems based on algorithmicself-assembly of DNA { a molecular fabrication technique that acts as a universal constructor that can inprinciple create complex structures by embedding universal computation within the self-assembly processes, thus guiding the assembly of components based on an information-processing algorithm implemented by themolecular tiles. This experimental and theoretical research has indicated that with current error rates as high as 10% and seldom lower than 1%, fault-tolerant techniques must be used when implementing biomolecularcomputing systems. The proposed research will develop such techniques for algorithmic DNA self-assembly by developing fault-tolerant tile sets that reduce major types of assembly error: (1) Proofreading tile sets, which correct errors that occur during normal growth, will be experimentally demonstrated, with the goal of achieving error rates less than 10
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