核糖核酸
折叠(DSP实现)
计算生物学
纳米技术
化学
计算机科学
生物
基因
遗传学
材料科学
工程类
电气工程
作者
Cody Geary,Paul W. K. Rothemund,Ebbe Sloth Andersen
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2014-08-14
卷期号:345 (6198): 799-804
被引量:373
标识
DOI:10.1126/science.1253920
摘要
Artificial DNA and RNA structures have been used as scaffolds for a variety of nanoscale devices. In comparison to DNA structures, RNA structures have been limited in size, but they also have advantages: RNA can fold during transcription and thus can be genetically encoded and expressed in cells. We introduce an architecture for designing artificial RNA structures that fold from a single strand, in which arrays of antiparallel RNA helices are precisely organized by RNA tertiary motifs and a new type of crossover pattern. We constructed RNA tiles that assemble into hexagonal lattices and demonstrated that lattices can be made by annealing and/or cotranscriptional folding. Tiles can be scaled up to 660 nucleotides in length, reaching a size comparable to that of large natural ribozymes.
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