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A helical amplification system composed of artificial nucleic acids

Herein we report an amplification system of helical excess triggered by nucleic acid hybridization for the first time. It is usually impossible to prepare achiral nanostructures composed of nucleic acids because of their intrinsic chirality. We used serinol nucleic acid (SNA) oligomers for the prepa...

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Autores principales: Kashida, Hiromu, Nishikawa, Keiji, Shi, Wenjing, Miyagawa, Toshiki, Yamashita, Hayato, Abe, Masayuki, Asanuma, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179025/
https://www.ncbi.nlm.nih.gov/pubmed/34163925
http://dx.doi.org/10.1039/d0sc05245k
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author Kashida, Hiromu
Nishikawa, Keiji
Shi, Wenjing
Miyagawa, Toshiki
Yamashita, Hayato
Abe, Masayuki
Asanuma, Hiroyuki
author_facet Kashida, Hiromu
Nishikawa, Keiji
Shi, Wenjing
Miyagawa, Toshiki
Yamashita, Hayato
Abe, Masayuki
Asanuma, Hiroyuki
author_sort Kashida, Hiromu
collection PubMed
description Herein we report an amplification system of helical excess triggered by nucleic acid hybridization for the first time. It is usually impossible to prepare achiral nanostructures composed of nucleic acids because of their intrinsic chirality. We used serinol nucleic acid (SNA) oligomers for the preparation of achiral nanowires because SNA oligomers with symmetrical sequences are achiral. Nanowire formation was confirmed by atomic force microscopy and size exclusion chromatography. When a chiral nucleic acid with a sequence complementary to SNA was added to the nanostructure, helicity was induced and a strong circular dichroism signal was observed. The SNA nanowire could amplify the helicity of chiral nucleic acids through nucleobase stacks. The SNA nanostructures have potential for use as platforms to detect chiral biomolecules under aqueous conditions because SNA can be readily functionalized and is water-soluble.
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spelling pubmed-81790252021-06-22 A helical amplification system composed of artificial nucleic acids Kashida, Hiromu Nishikawa, Keiji Shi, Wenjing Miyagawa, Toshiki Yamashita, Hayato Abe, Masayuki Asanuma, Hiroyuki Chem Sci Chemistry Herein we report an amplification system of helical excess triggered by nucleic acid hybridization for the first time. It is usually impossible to prepare achiral nanostructures composed of nucleic acids because of their intrinsic chirality. We used serinol nucleic acid (SNA) oligomers for the preparation of achiral nanowires because SNA oligomers with symmetrical sequences are achiral. Nanowire formation was confirmed by atomic force microscopy and size exclusion chromatography. When a chiral nucleic acid with a sequence complementary to SNA was added to the nanostructure, helicity was induced and a strong circular dichroism signal was observed. The SNA nanowire could amplify the helicity of chiral nucleic acids through nucleobase stacks. The SNA nanostructures have potential for use as platforms to detect chiral biomolecules under aqueous conditions because SNA can be readily functionalized and is water-soluble. The Royal Society of Chemistry 2021-01-12 /pmc/articles/PMC8179025/ /pubmed/34163925 http://dx.doi.org/10.1039/d0sc05245k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kashida, Hiromu
Nishikawa, Keiji
Shi, Wenjing
Miyagawa, Toshiki
Yamashita, Hayato
Abe, Masayuki
Asanuma, Hiroyuki
A helical amplification system composed of artificial nucleic acids
title A helical amplification system composed of artificial nucleic acids
title_full A helical amplification system composed of artificial nucleic acids
title_fullStr A helical amplification system composed of artificial nucleic acids
title_full_unstemmed A helical amplification system composed of artificial nucleic acids
title_short A helical amplification system composed of artificial nucleic acids
title_sort helical amplification system composed of artificial nucleic acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179025/
https://www.ncbi.nlm.nih.gov/pubmed/34163925
http://dx.doi.org/10.1039/d0sc05245k
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