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Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion

The application of DNA as a functional material such as DNA hydrogel has attracted much attention. Despite an increasing interest, the high cost of DNA synthesis is a limiting factor for its utilization. To reduce the cost, we report here a highly efficient amplification technique for polypod-like s...

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Autores principales: Yata, Tomoya, Takahashi, Yuki, Tan, Mengmeng, Hidaka, Kumi, Sugiyama, Hiroshi, Endo, Masayuki, Takakura, Yoshinobu, Nishikawa, Makiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604513/
https://www.ncbi.nlm.nih.gov/pubmed/26462616
http://dx.doi.org/10.1038/srep14979
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author Yata, Tomoya
Takahashi, Yuki
Tan, Mengmeng
Hidaka, Kumi
Sugiyama, Hiroshi
Endo, Masayuki
Takakura, Yoshinobu
Nishikawa, Makiya
author_facet Yata, Tomoya
Takahashi, Yuki
Tan, Mengmeng
Hidaka, Kumi
Sugiyama, Hiroshi
Endo, Masayuki
Takakura, Yoshinobu
Nishikawa, Makiya
author_sort Yata, Tomoya
collection PubMed
description The application of DNA as a functional material such as DNA hydrogel has attracted much attention. Despite an increasing interest, the high cost of DNA synthesis is a limiting factor for its utilization. To reduce the cost, we report here a highly efficient amplification technique for polypod-like structured DNA (polypodna) with adhesive ends that spontaneously forms DNA hydrogel. Two types of polypodna with three (tripodna) and four (tetrapodna) pods were selected, and a template oligodeoxynucleotide, containing a tandem sequence of a looped tripodna or tetrapodna, respectively, along with restriction enzyme (TspRI) sites, was designed. The template was circularized using T4 DNA ligase, and amplified by rolling circle amplification (RCA). The RCA product was highly viscous and resistant to restriction digestion. Observation under an electron microscope revealed microflower-like structures. These structures were composed of long DNA and magnesium pyrophosphate, and their treatment with EDTA followed by restriction digestion with TspRI resulted in numerous copies of polypodna with adhesive ends, which formed a DNA hydrogel. Thus, we believe this technique provides a new approach to produce DNA nanostructures, and helps in expanding their practical applications.
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spelling pubmed-46045132015-12-07 Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion Yata, Tomoya Takahashi, Yuki Tan, Mengmeng Hidaka, Kumi Sugiyama, Hiroshi Endo, Masayuki Takakura, Yoshinobu Nishikawa, Makiya Sci Rep Article The application of DNA as a functional material such as DNA hydrogel has attracted much attention. Despite an increasing interest, the high cost of DNA synthesis is a limiting factor for its utilization. To reduce the cost, we report here a highly efficient amplification technique for polypod-like structured DNA (polypodna) with adhesive ends that spontaneously forms DNA hydrogel. Two types of polypodna with three (tripodna) and four (tetrapodna) pods were selected, and a template oligodeoxynucleotide, containing a tandem sequence of a looped tripodna or tetrapodna, respectively, along with restriction enzyme (TspRI) sites, was designed. The template was circularized using T4 DNA ligase, and amplified by rolling circle amplification (RCA). The RCA product was highly viscous and resistant to restriction digestion. Observation under an electron microscope revealed microflower-like structures. These structures were composed of long DNA and magnesium pyrophosphate, and their treatment with EDTA followed by restriction digestion with TspRI resulted in numerous copies of polypodna with adhesive ends, which formed a DNA hydrogel. Thus, we believe this technique provides a new approach to produce DNA nanostructures, and helps in expanding their practical applications. Nature Publishing Group 2015-10-14 /pmc/articles/PMC4604513/ /pubmed/26462616 http://dx.doi.org/10.1038/srep14979 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yata, Tomoya
Takahashi, Yuki
Tan, Mengmeng
Hidaka, Kumi
Sugiyama, Hiroshi
Endo, Masayuki
Takakura, Yoshinobu
Nishikawa, Makiya
Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion
title Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion
title_full Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion
title_fullStr Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion
title_full_unstemmed Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion
title_short Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion
title_sort efficient amplification of self-gelling polypod-like structured dna by rolling circle amplification and enzymatic digestion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604513/
https://www.ncbi.nlm.nih.gov/pubmed/26462616
http://dx.doi.org/10.1038/srep14979
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