Sequence-specific recognition of DNA nanostructures
Sequence-specific recognition of DNA nanostructures
DNA is the most exploited biopolymer for the programmed self-assembly of objects and devices that exhibit nanoscale-sized features. One of the most useful properties of DNA nanostructures is their ability to be functionalized with additional non-nucleic acid components. The introduction of such a component is often achieved by attaching it to an oligonucleotide that is part of the nanostructure, or hybridizing it to single-stranded overhangs that extend beyond or above the nanostructure surface. However, restrictions in nanostructure design and/or the self-assembly process can limit the suitability of these procedures. An alternative strategy is to couple the component to a DNA recognition agent that is capable of binding to duplex sequences within the nanostructure. This offers the advantage that it requires little, if any, alteration to the nanostructure and can be achieved after structure assembly. In addition, since the molecular recognition of DNA can be controlled by varying pH and ionic conditions, such systems offer tunable properties that are distinct from simple Watson–Crick hybridization. Here, we describe methodology that has been used to exploit and characterize the sequence-specific recognition of DNA nanostructures, with the aim of generating functional assemblies for bionanotechnology and synthetic biology applications.
dna nanostructure, self-assembly, crossover
1-11
Rusling, David A.
d08f1f97-f8a9-4980-a025-ae41c23a938f
Fox, Keith R.
9da5debc-4e45-473e-ab8c-550d1104659f
28 February 2014
Rusling, David A.
d08f1f97-f8a9-4980-a025-ae41c23a938f
Fox, Keith R.
9da5debc-4e45-473e-ab8c-550d1104659f
Abstract
DNA is the most exploited biopolymer for the programmed self-assembly of objects and devices that exhibit nanoscale-sized features. One of the most useful properties of DNA nanostructures is their ability to be functionalized with additional non-nucleic acid components. The introduction of such a component is often achieved by attaching it to an oligonucleotide that is part of the nanostructure, or hybridizing it to single-stranded overhangs that extend beyond or above the nanostructure surface. However, restrictions in nanostructure design and/or the self-assembly process can limit the suitability of these procedures. An alternative strategy is to couple the component to a DNA recognition agent that is capable of binding to duplex sequences within the nanostructure. This offers the advantage that it requires little, if any, alteration to the nanostructure and can be achieved after structure assembly. In addition, since the molecular recognition of DNA can be controlled by varying pH and ionic conditions, such systems offer tunable properties that are distinct from simple Watson–Crick hybridization. Here, we describe methodology that has been used to exploit and characterize the sequence-specific recognition of DNA nanostructures, with the aim of generating functional assemblies for bionanotechnology and synthetic biology applications.
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Published date: 28 February 2014
Keywords:
dna nanostructure, self-assembly, crossover
Organisations:
Molecular and Cellular
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Local EPrints ID: 363326
URI: http://eprints.soton.ac.uk/id/eprint/363326
ISSN: 1046-2023
PURE UUID: 5773f778-5153-41b7-9d23-c3468f0da164
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Date deposited: 24 Mar 2014 13:27
Last modified: 15 Mar 2024 02:36
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Author:
David A. Rusling
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