Published March 2020 | Version Submitted
Journal Article Open

Branched kissing loops for the construction of diverse RNA homooligomeric nanostructures

  • 1. ROR icon University of Chicago
  • 2. ROR icon Aarhus University
  • 3. ROR icon California Institute of Technology
  • 4. ROR icon University of Central Florida
  • 5. ROR icon Purdue University West Lafayette
  • 6. ROR icon Ben-Gurion University of the Negev

Abstract

In biological systems, large and complex structures are often assembled from multiple simpler identical subunits. This strategy—homooligomerization—allows efficient genetic encoding of structures and avoids the need to control the stoichiometry of multiple distinct units. It also allows the minimal number of distinct subunits when designing artificial nucleic acid structures. Here, we present a robust self-assembly system in which homooligomerizable tiles are formed from intramolecularly folded RNA single strands. Tiles are linked through an artificially designed branched kissing-loop motif, involving Watson–Crick base pairing between the single-stranded regions of a bulged helix and a hairpin loop. By adjusting the tile geometry to gain control over the curvature, torsion and the number of helices, we have constructed 16 different linear and circular structures, including a finite-sized three-dimensional cage. We further demonstrate cotranscriptional self-assembly of tiles based on branched kissing loops, and show that tiles inserted into a transfer RNA scaffold can be overexpressed in bacterial cells.

Additional Information

© The Author(s), under exclusive licence to Springer Nature Limited 2020. Received: 25 February 2019; Accepted: 6 December 2019; Published: 20 January 2020. D.L. acknowledges the HHMI International Student Research Fellowship. C.W.G. acknowledges a fellowship from the Carlsberg Research Foundation. This work was supported by NSF CAREER Award (DMR-1555361) to Y.W., NIH grant (R01GM102489) to J.A.P., ERC grant (683305) to E.S.A. and NSF grants (CCF-1317694 and CMMI-1636364) and ONR grants (N00014-16-1-2159, N00014-17-1-2610 and N00014-18-1-2649) to P.W.K.R. Cryo-EM experiments were conducted with the Structural Biology Facility at Northwestern University, and we thank J. Remis for assistance. We thank N.-s. Li for synthesizing DFHBI. We thank P. Yin for sharing unpublished results based on bKL and helpful discussions. Author Contributions: D.L. and Y.W. conceived the project. D.L., C.W.G., G.C., Y.S. and M.L. performed the research. C.M., E.S.A., J.A.P., P.W.K.R. and Y.W. supervised the project. D.L., C.W.G., P.W.K.R. and Y.W. wrote the manuscript. All authors analysed the data and commented on the manuscript. Data availability: The data supporting the findings of this study are principally within the figures and the associated Supplementary Information. Additional data are available from the authors upon request. The authors declare no competing interests.

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Submitted - Branched_Kissing_Loops_for_the_Construction_of_Diverse_RNA_Homooligomeric_Nanostructures_v1.pdf

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Branched_Kissing_Loops_for_the_Construction_of_Diverse_RNA_Homooligomeric_Nanostructures_v1.pdf

Additional details

Identifiers

Eprint ID
99301
Resolver ID
CaltechAUTHORS:20191016-120007639

Related works

Funding

Howard Hughes Medical Institute (HHMI)
Carlsberg Research Foundation
NSF
DMR-1555361
NIH
R01GM102489
European Research Council (ERC)
683305
NSF
CCF-1317694
NSF
CMMI-1636364
Office of Naval Research (ONR)
N00014-16-1-2159
Office of Naval Research (ONR)
N00014-17-1-2610
Office of Naval Research (ONR)
N00014-18-1-2649

Dates

Created
2019-10-16
Created from EPrint's datestamp field
Updated
2023-06-01
Created from EPrint's last_modified field