Vid Kočar (Author), John S. Schreck (Author), Slavko Čeru (Author), Helena Gradišar (Author), Nino Bašić (Author), Tomaž Pisanski (Author), Jonathan P. K. Doye (Author), Roman Jerala (Author)

Abstract

Knots are some of the most remarkable topological features in nature. Self-assembly of knotted polymers without breaking or forming covalent bonds is challenging, as the chain needs to be threaded through previously formed loops in an exactly defined order. Here we describe principles to guide the folding of highly knotted single-chain DNA nanostructures as demonstrated on a nano-sized square pyramid. Folding of knots is encoded by the arrangement of modules of different stability based on derived topological and kinetic rules. Among DNA designs composed of the same modules and encoding the same topology, only the one with the folding pathway designed according to the "free-end" rule folds efficiently into the target structure. Besides high folding yield on slow annealing, this design also folds rapidly on temperature quenching and dilution from chemical denaturant. This strategy could be used to design folding of other knotted programmable polymers such as RNA or proteins.

Keywords

biokemija;DNA;nanostrukture;struktura snovi;

Data

Language: English
Year of publishing:
Typology: 1.01 - Original Scientific Article
Organization: KI - National Institute of Chemistry
UDC: 577.2
COBISS: 5880858 Link will open in a new window
ISSN: 2041-1723
Views: 3738
Downloads: 1108
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Other data

Secondary keywords: biokemija;DNA;nanostrukture;struktura snovi;
Type (COBISS): Article
Source comment: Sodelavci: John S. Schreck, Slavko Čeru, Helena Gradišar, Nino Bašić, Tomaž Pisanski, Jonathan P. K. Doye & Roman Jerala; Opis vira z dne 7. 3. 2016; Nasl. z nasl. zaslona; Št. članka 10803;
Pages: str. 1-8
Issue: ǂVol. ǂ7
Chronology: Feb. 2016
DOI: 10.1038/ncomms10803
ID: 9145169
Recommended works:
, lecture at the Konan University, FIBER Future College, 22. 6. 2015
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