| Literature DB >> 26322946 |
Jakob Bach Knudsen1,2, Lei Liu1, Anne Louise Bank Kodal1,2, Mikael Madsen1,2, Qiang Li1, Jie Song1, Johannes B Woehrstein3,4, Shelley F J Wickham3, Maximilian T Strauss3,4, Florian Schueder3, Jesper Vinther1,2, Abhichart Krissanaprasit1, Daniel Gudnason1, Anton Allen Abbotsford Smith2, Ryosuke Ogaki1, Alexander N Zelikin2, Flemming Besenbacher1, Victoria Birkedal1, Peng Yin3,5, William M Shih3, Ralf Jungmann3,4,5, Mingdong Dong1, Kurt V Gothelf1,2.
Abstract
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.Entities:
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Year: 2015 PMID: 26322946 DOI: 10.1038/nnano.2015.190
Source DB: PubMed Journal: Nat Nanotechnol ISSN: 1748-3387 Impact factor: 39.213