Published August 15, 2014 | Version Supplemental Material
Journal Article Open

A single-stranded architecture for cotranscriptional folding of RNA nanostructures

Abstract

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.

Additional Information

© 2014 American Association for the Advancement of Science. Received for publication 25 March 2014. Accepted for publication 16 June 2014. The authors thank E. Winfree and M. Dong for use of their AFM facilities. We acknowledge financial support from the Danish Council for Independent Research (Sapere Aude Starting Grant DFF-0602-01772), the Danish National Research Foundation funding Centre for DNA Nanotechnology (grant DNRF81, http://cdna.au.dk/), the U.S. National Science Foundation for Expeditions in Computing funding for the Molecular Programming Project (grant nos. 0832824 and 1317694, http://molecular-programming.org), and Army Research Office award W911NF-11-1-0117. C.G., P.W.K.R., and E.S.A planned experiments and wrote the paper together. C.G. performed all experiments. The authors declare no competing financial interests.

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Additional details

Identifiers

Eprint ID
48753
Resolver ID
CaltechAUTHORS:20140820-190801194

Funding

Danish Council for Independent Research
DFF-0602-01772
Danish National Research Foundation
DNRF81
NSF
0832824
NSF
1317694
Army Research Office (ARO)
W911NF-11-1-0117

Dates

Created
2014-08-21
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Updated
2021-11-10
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