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Routing of individual polymers in designed patterns

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DOI

  • Jakob Bach Knudsen, Danmark
  • Lei Liu, Danmark
  • Anne Louise Bank Kodal, Danmark
  • Mikael Madsen, Danmark
  • Qiang Li, Kina
  • Jie Song, Danmark
  • Johannes Woehrstein, Danmark
  • Shelley Wickham, Danmark
  • Maximillian Strauss, Danmark
  • Florian Schueder, Danmark
  • Jesper Vinther, Danmark
  • Abhichart Krissanaprasit, Danmark
  • Daniel Aron Gudnason, Danmark
  • Anton Allen Abbotsford Smith, Danmark
  • Ryosuke Ogaki, Danmark
  • Alexander N. Zelikin
  • Flemming Besenbacher
  • Victoria Birkedal
  • Peng Yin, Ukendt
  • William M. Shih, Harvard Medical School, USA
  • Ralf Jungmann, Danmark
  • Mingdong Dong
  • Kurt Vesterager Gothelf
Synthetic polymers are ubiquitous in the modern world, but our ability to exert control over the molecular conformation of individual polymers is very limited. In particular, although the programmable self-assembly of oligonucleotides and proteins into artificial nanostructures has been demonstrated, we currently lack the tools to handle other types of synthetic polymers individually and thus the ability to utilize and study their single-molecule properties. Here we show that synthetic polymer wires containing short oligonucleotides that extend from each repeat can be made to assemble into arbitrary routings. The wires, which can be more than 200 nm in length, are soft and bendable, and the DNA strands allow individual polymers to self-assemble into predesigned routings on both two- and three-dimensional DNA origami templates. The polymers are conjugated and potentially conducting, and could therefore be used to create molecular-scale electronic or optical wires in arbitrary geometries.
OriginalsprogDansk
TidsskriftNature Nanotechnology
Vol/bind10
Sider (fra-til)892-898
ISSN1748-3387
DOI
StatusUdgivet - 31 aug. 2015

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