A large size-selective DNA nanopore with sensing applications

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  • Rasmus P. Thomsen
  • ,
  • Mette Galsgaard Malle, Københavns Universitet
  • ,
  • Anders Hauge Okholm, Arla Innovation Centre
  • ,
  • Swati Krishnan, Technical University of Munich
  • ,
  • Søren S.R. Bohr, Københavns Universitet
  • ,
  • Rasmus Schøler Sørensen
  • ,
  • Oliver Ries, Syddansk Universitet
  • ,
  • Stefan Vogel, Syddansk Universitet
  • ,
  • Friedrich C. Simmel, Technical University of Munich
  • ,
  • Nikos S. Hatzakis, Københavns Universitet
  • ,
  • Jørgen Kjems

Transmembrane nanostructures like ion channels and transporters perform key biological functions by controlling flow of molecules across lipid bilayers. Much work has gone into engineering artificial nanopores and applications in selective gating of molecules, label-free detection/sensing of biomolecules and DNA sequencing have shown promise. Here, we use DNA origami to create a synthetic 9 nm wide DNA nanopore, controlled by programmable, lipidated flaps and equipped with a size-selective gating system for the translocation of macromolecules. Successful assembly and insertion of the nanopore into lipid bilayers are validated by transmission electron microscopy (TEM), while selective translocation of cargo and the pore mechanosensitivity are studied using optical methods, including single-molecule, total internal reflection fluorescence (TIRF) microscopy. Size-specific cargo translocation and oligonucleotide-triggered opening of the pore are demonstrated showing that the DNA nanopore can function as a real-time detection system for external signals, offering potential for a variety of highly parallelized sensing applications.

Original languageEnglish
Article number5655
JournalNature Communications
Volume10
Issue1
ISSN2041-1723
DOIs
Publication statusPublished - Dec 2019

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