A single-stranded architecture for cotranscriptional folding of RNA nanostructures

被引:258
|
作者
Geary, Cody [1 ,2 ]
Rothemund, Paul W. K. [3 ]
Andersen, Ebbe S. [1 ,2 ]
机构
[1] Aarhus Univ, Ctr DNA Nanotechnol, Interdisciplinary Nanosci Ctr, DK-8000 Aarhus, Denmark
[2] Aarhus Univ, Dept Mol Biol & Genet, DK-8000 Aarhus, Denmark
[3] CALTECH, Pasadena, CA 91125 USA
基金
新加坡国家研究基金会; 美国国家科学基金会;
关键词
DNA NANOSTRUCTURES; COMPLEX; DESIGN; ACID; NANOTECHNOLOGY; ASSEMBLIES; JUNCTIONS; SEQUENCE; SHAPES; FORM;
D O I
10.1126/science.1253920
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
收藏
页码:799 / 804
页数:6
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