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PMID: 11139616 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

TectoRNA: modular assembly units for the construction of RNA nano-objects.

Nucleic acids research ·Vol. 29 ·No. 2 ·2001-01-15 ·Pages 455-63

Jaeger L, Westhof E, Leontis NB

Abstract

Structural information on complex biological RNA molecules can be exploited to design tectoRNAs or artificial modular RNA units that can self-assemble through tertiary interactions thereby forming nanoscale RNA objects. The selective interactions of hairpin tetraloops with their receptors can be used to mediate tectoRNA assembly. Here we report on the modulation of the specificity and the strength of tectoRNA assembly (in the nanomolar to micromolar range) by variation of the length of the RNA subunits, the nature of their interacting motifs and the degree of flexibility of linker regions incorporated into the molecules. The association is also dependent on the concentration of magnesium. Monitoring of tectoRNA assembly by lead(II) cleavage protection indicates that some degree of structural flexibility is required for optimal binding. With tectoRNAs one can compare the binding affinities of different tertiary motifs and quantify the strength of individual interactions. Furthermore, in analogy to the synthons used in organic chemistry to synthesize more complex organic compounds, tectoRNAs form the basic assembly units for constructing complex RNA structures on the nanometer scale. Thus, tectoRNA provides a means for constructing molecular scaffoldings that organize functional modules in three-dimensional space for a wide range of applications.

MeSH Terms
Base Composition/drug effects Base Sequence Crystallography, X-Ray Dimerization Genetic Engineering/methods Hydrolysis Kinetics Lead/pharmacology Microchemistry/methods Models, Molecular Molecular Sequence Data Nucleic Acid Conformation/drug effects Particle Size RNA/chemical synthesis,metabolism Thermodynamics
Chemicals
Lead lead chloride RNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jaeger L
Institut de Biologie Moléculaire et Cellulaire, UPR 9002 du CNRS, 15 rue René Descartes, F-67084 Strasbourg Cedex, France. [email protected]
Westhof E
Leontis N B
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
1362-4962
Published
2001-01-15
Pages
455-63
Language
English
Region
England
NLM ID
0411011
PMCID
PMC29663
Subset
IM
Grants
FIC NIH HHS · F06 TW002251 · United States
NIGMS NIH HHS · R15 GM055898 · United States
FIC NIH HHS · 1-F06-TW02251-01 · United States
NIGMS NIH HHS · 1R15 GM55898 · United States
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