Artificial rna motifs expand the programmable assembly between RNA modules of a bimolecular ribozyme leading to application to RNA nanostructure design

Md Motiar Rahman*, Shigeyoshi Matsumura, Yoshiya Ikawa

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

A bimolecular ribozyme consisting of a core ribozyme (ΔP5 RNA) and an activator module (P5abc RNA) has been used as a platform to design assembled RNA nanostructures. The tight and specific assembly between the P5abc and ΔP5 modules depends on two sets of intermodule interactions. The interface between P5abc and ΔP5 must be controlled when designing RNA nanostructures. To expand the repertoire of molecular recognition in the P5abc/ΔP5 interface, we modified the interface by replacing the parent tertiary interactions in the interface with artificial interactions. The engineered P5abc/ΔP5 interfaces were characterized biochemically to identify those suitable for nanostructure design. The new interfaces were used to construct 2D-square and 1D-array RNA nanostructures.

Original languageEnglish
Article number37
JournalBiology
Volume6
Issue number4
DOIs
StatePublished - 2017/12

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology
  • General Agricultural and Biological Sciences

Fingerprint

Dive into the research topics of 'Artificial rna motifs expand the programmable assembly between RNA modules of a bimolecular ribozyme leading to application to RNA nanostructure design'. Together they form a unique fingerprint.

Cite this