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Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions

Unnatural nucleosides have been explored to expand the properties and the applications of oligonucleotides. This paper briefly summarizes nucleic acid analogs in which the base is modified or replaced by an unnatural stacking group for the study of nucleic acid interactions. We also describe the nuc...

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Autores principales: Nakano, Shu-ichi, Fujii, Masayuki, Sugimoto, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142669/
https://www.ncbi.nlm.nih.gov/pubmed/21822475
http://dx.doi.org/10.4061/2011/967098
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author Nakano, Shu-ichi
Fujii, Masayuki
Sugimoto, Naoki
author_facet Nakano, Shu-ichi
Fujii, Masayuki
Sugimoto, Naoki
author_sort Nakano, Shu-ichi
collection PubMed
description Unnatural nucleosides have been explored to expand the properties and the applications of oligonucleotides. This paper briefly summarizes nucleic acid analogs in which the base is modified or replaced by an unnatural stacking group for the study of nucleic acid interactions. We also describe the nucleoside analogs of a base pair-mimic structure that we have examined. Although the base pair-mimic nucleosides possess a simplified stacking moiety of a phenyl or naphthyl group, they can be used as a structural analog of Watson-Crick base pairs. Remarkably, they can adopt two different conformations responding to their interaction energies, and one of them is the stacking conformation of the nonpolar aromatic group causing the site-selective flipping of the opposite base in a DNA double helix. The base pair-mimic nucleosides can be used to study the mechanism responsible for the base stacking and the flipping of bases out of a nucleic acid duplex.
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spelling pubmed-31426692011-08-05 Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions Nakano, Shu-ichi Fujii, Masayuki Sugimoto, Naoki J Nucleic Acids Review Article Unnatural nucleosides have been explored to expand the properties and the applications of oligonucleotides. This paper briefly summarizes nucleic acid analogs in which the base is modified or replaced by an unnatural stacking group for the study of nucleic acid interactions. We also describe the nucleoside analogs of a base pair-mimic structure that we have examined. Although the base pair-mimic nucleosides possess a simplified stacking moiety of a phenyl or naphthyl group, they can be used as a structural analog of Watson-Crick base pairs. Remarkably, they can adopt two different conformations responding to their interaction energies, and one of them is the stacking conformation of the nonpolar aromatic group causing the site-selective flipping of the opposite base in a DNA double helix. The base pair-mimic nucleosides can be used to study the mechanism responsible for the base stacking and the flipping of bases out of a nucleic acid duplex. SAGE-Hindawi Access to Research 2011-07-24 /pmc/articles/PMC3142669/ /pubmed/21822475 http://dx.doi.org/10.4061/2011/967098 Text en Copyright © 2011 Shu-ichi Nakano et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Nakano, Shu-ichi
Fujii, Masayuki
Sugimoto, Naoki
Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions
title Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions
title_full Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions
title_fullStr Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions
title_full_unstemmed Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions
title_short Use of Nucleic Acid Analogs for the Study of Nucleic Acid Interactions
title_sort use of nucleic acid analogs for the study of nucleic acid interactions
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142669/
https://www.ncbi.nlm.nih.gov/pubmed/21822475
http://dx.doi.org/10.4061/2011/967098
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