4.4 Article

Dynamic Chemistry of Disulfide Terminated Oligonucleotides in Duplexes and Double-Crossover Tiles

Journal

CHEMBIOCHEM
Volume 17, Issue 12, Pages 1122-1126

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201600076

Keywords

disulfides; DNA structures; dynamic combinatorial chemistry; nucleic acids; reduction

Funding

  1. Danish National Research Foundation [DNRF81]
  2. European School of DNA Nanotechnology (EScoDNA), a Marie Curie ITN under FP7

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Designed nanostructures formed by self-assembly of multiple DNA strands suffer from low stability at elevated temperature and under other denaturing conditions. Here, we propose a method for covalent coupling of DNA strands in such structures by the formation of disulfide bonds; this allows disassembly of the structure under reducing conditions. The dynamic chemistry of disulfides and thiols was applied to crosslink DNA strands with terminal disulfide modifications. The formation of disulfide-linked DNA duplexes consisting of three strands is demonstrated, as well as a more-complex DNA double-crossover tile. All the strands in the fully disulfide-linked structures are covalently and geometrically interlocked, and it is demonstrated that the structures are stable under heating and in the presence of denaturants. Such a reversible system can be exploited in applications where higher DNA stability is needed only temporarily, such as delivery of cargoes to cells by DNA nanostructures.

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