Triggering nucleic acid nanostructure assembly by conditional kissing interactions

Nucleic Acids Res. 2018 Feb 16;46(3):1052-1058. doi: 10.1093/nar/gkx1267.

Abstract

Nucleic acids are biomolecules of amazing versatility. Beyond their function for information storage they can be used for building nano-objects. We took advantage of loop-loop or kissing interactions between hairpin building blocks displaying complementary loops for driving the assembly of nucleic acid nano-architectures. It is of interest to make the interaction between elementary units dependent on an external trigger, thus allowing the control of the scaffold formation. To this end we exploited the binding properties of structure-switching aptamers (aptaswitch). Aptaswitches are stem-loop structured oligonucleotides that engage a kissing complex with an RNA hairpin in response to ligand-induced aptaswitch folding. We demonstrated the potential of this approach by conditionally assembling oligonucleotide nanorods in response to the addition of adenosine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / chemistry*
  • Aptamers, Nucleotide / chemistry*
  • Base Pairing
  • Base Sequence
  • Binding Sites
  • DNA / chemistry*
  • Inverted Repeat Sequences
  • Ligands
  • Nanotechnology / methods
  • Nanotubes / chemistry*
  • Nanotubes / ultrastructure
  • Nucleic Acid Conformation
  • Oligonucleotides / chemistry*
  • RNA / chemistry*

Substances

  • Aptamers, Nucleotide
  • Ligands
  • Oligonucleotides
  • RNA
  • DNA
  • Adenosine