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Structure, stability and behaviour of nucleic acids in ionic liquids

Nucleic acids have become a powerful tool in nanotechnology because of their conformational polymorphism. However, lack of a medium in which nucleic acid structures exhibit long-term stability has been a bottleneck. Ionic liquids (ILs) are potential solvents in the nanotechnology field. Hydrated ILs...

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Autores principales: Tateishi-Karimata, Hisae, Sugimoto, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132699/
https://www.ncbi.nlm.nih.gov/pubmed/25013178
http://dx.doi.org/10.1093/nar/gku499
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author Tateishi-Karimata, Hisae
Sugimoto, Naoki
author_facet Tateishi-Karimata, Hisae
Sugimoto, Naoki
author_sort Tateishi-Karimata, Hisae
collection PubMed
description Nucleic acids have become a powerful tool in nanotechnology because of their conformational polymorphism. However, lack of a medium in which nucleic acid structures exhibit long-term stability has been a bottleneck. Ionic liquids (ILs) are potential solvents in the nanotechnology field. Hydrated ILs, such as choline dihydrogen phosphate (choline dhp) and deep eutectic solvent (DES) prepared from choline chloride and urea, are ‘green’ solvents that ensure long-term stability of biomolecules. An understanding of the behaviour of nucleic acids in hydrated ILs is necessary for developing DNA materials. We here review current knowledge about the structures and stabilities of nucleic acids in choline dhp and DES. Interestingly, in choline dhp, A–T base pairs are more stable than G–C base pairs, the reverse of the situation in buffered NaCl solution. Moreover, DNA triplex formation is markedly stabilized in hydrated ILs compared with aqueous solution. In choline dhp, the stability of Hoogsteen base pairs is comparable to that of Watson–Crick base pairs. Moreover, the parallel form of the G-quadruplex is stabilized in DES compared with aqueous solution. The behaviours of various DNA molecules in ILs detailed here should be useful for designing oligonucleotides for the development of nanomaterials and nanodevices.
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spelling pubmed-41326992014-12-01 Structure, stability and behaviour of nucleic acids in ionic liquids Tateishi-Karimata, Hisae Sugimoto, Naoki Nucleic Acids Res Survey and Summary Nucleic acids have become a powerful tool in nanotechnology because of their conformational polymorphism. However, lack of a medium in which nucleic acid structures exhibit long-term stability has been a bottleneck. Ionic liquids (ILs) are potential solvents in the nanotechnology field. Hydrated ILs, such as choline dihydrogen phosphate (choline dhp) and deep eutectic solvent (DES) prepared from choline chloride and urea, are ‘green’ solvents that ensure long-term stability of biomolecules. An understanding of the behaviour of nucleic acids in hydrated ILs is necessary for developing DNA materials. We here review current knowledge about the structures and stabilities of nucleic acids in choline dhp and DES. Interestingly, in choline dhp, A–T base pairs are more stable than G–C base pairs, the reverse of the situation in buffered NaCl solution. Moreover, DNA triplex formation is markedly stabilized in hydrated ILs compared with aqueous solution. In choline dhp, the stability of Hoogsteen base pairs is comparable to that of Watson–Crick base pairs. Moreover, the parallel form of the G-quadruplex is stabilized in DES compared with aqueous solution. The behaviours of various DNA molecules in ILs detailed here should be useful for designing oligonucleotides for the development of nanomaterials and nanodevices. Oxford University Press 2014-08-18 2014-07-10 /pmc/articles/PMC4132699/ /pubmed/25013178 http://dx.doi.org/10.1093/nar/gku499 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Survey and Summary
Tateishi-Karimata, Hisae
Sugimoto, Naoki
Structure, stability and behaviour of nucleic acids in ionic liquids
title Structure, stability and behaviour of nucleic acids in ionic liquids
title_full Structure, stability and behaviour of nucleic acids in ionic liquids
title_fullStr Structure, stability and behaviour of nucleic acids in ionic liquids
title_full_unstemmed Structure, stability and behaviour of nucleic acids in ionic liquids
title_short Structure, stability and behaviour of nucleic acids in ionic liquids
title_sort structure, stability and behaviour of nucleic acids in ionic liquids
topic Survey and Summary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132699/
https://www.ncbi.nlm.nih.gov/pubmed/25013178
http://dx.doi.org/10.1093/nar/gku499
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