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Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate

Nucleic acid nanotechnology has great potential for future therapeutic applications. However, the construction of nanostructured devices that control cell fate by detecting and amplifying protein signals has remained a challenge. Here we design and build protein-driven RNA-nanostructured devices tha...

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Autores principales: Shibata, Tomonori, Fujita, Yoshihiko, Ohno, Hirohisa, Suzuki, Yuki, Hayashi, Karin, Komatsu, Kaoru R., Kawasaki, Shunsuke, Hidaka, Kumi, Yonehara, Shin, Sugiyama, Hiroshi, Endo, Masayuki, Saito, Hirohide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599586/
https://www.ncbi.nlm.nih.gov/pubmed/28912471
http://dx.doi.org/10.1038/s41467-017-00459-x
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author Shibata, Tomonori
Fujita, Yoshihiko
Ohno, Hirohisa
Suzuki, Yuki
Hayashi, Karin
Komatsu, Kaoru R.
Kawasaki, Shunsuke
Hidaka, Kumi
Yonehara, Shin
Sugiyama, Hiroshi
Endo, Masayuki
Saito, Hirohide
author_facet Shibata, Tomonori
Fujita, Yoshihiko
Ohno, Hirohisa
Suzuki, Yuki
Hayashi, Karin
Komatsu, Kaoru R.
Kawasaki, Shunsuke
Hidaka, Kumi
Yonehara, Shin
Sugiyama, Hiroshi
Endo, Masayuki
Saito, Hirohide
author_sort Shibata, Tomonori
collection PubMed
description Nucleic acid nanotechnology has great potential for future therapeutic applications. However, the construction of nanostructured devices that control cell fate by detecting and amplifying protein signals has remained a challenge. Here we design and build protein-driven RNA-nanostructured devices that actuate in vitro by RNA-binding-protein-inducible conformational change and regulate mammalian cell fate by RNA–protein interaction-mediated protein assembly. The conformation and function of the RNA nanostructures are dynamically controlled by RNA-binding protein signals. The protein-responsive RNA nanodevices are constructed inside cells using RNA-only delivery, which may provide a safe tool for building functional RNA–protein nanostructures. Moreover, the designed RNA scaffolds that control the assembly and oligomerization of apoptosis-regulatory proteins on a nanometre scale selectively kill target cells via specific RNA–protein interactions. These findings suggest that synthetic RNA nanodevices could function as molecular robots that detect signals and localize target proteins, induce RNA conformational changes, and programme mammalian cellular behaviour.
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spelling pubmed-55995862017-09-18 Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate Shibata, Tomonori Fujita, Yoshihiko Ohno, Hirohisa Suzuki, Yuki Hayashi, Karin Komatsu, Kaoru R. Kawasaki, Shunsuke Hidaka, Kumi Yonehara, Shin Sugiyama, Hiroshi Endo, Masayuki Saito, Hirohide Nat Commun Article Nucleic acid nanotechnology has great potential for future therapeutic applications. However, the construction of nanostructured devices that control cell fate by detecting and amplifying protein signals has remained a challenge. Here we design and build protein-driven RNA-nanostructured devices that actuate in vitro by RNA-binding-protein-inducible conformational change and regulate mammalian cell fate by RNA–protein interaction-mediated protein assembly. The conformation and function of the RNA nanostructures are dynamically controlled by RNA-binding protein signals. The protein-responsive RNA nanodevices are constructed inside cells using RNA-only delivery, which may provide a safe tool for building functional RNA–protein nanostructures. Moreover, the designed RNA scaffolds that control the assembly and oligomerization of apoptosis-regulatory proteins on a nanometre scale selectively kill target cells via specific RNA–protein interactions. These findings suggest that synthetic RNA nanodevices could function as molecular robots that detect signals and localize target proteins, induce RNA conformational changes, and programme mammalian cellular behaviour. Nature Publishing Group UK 2017-09-14 /pmc/articles/PMC5599586/ /pubmed/28912471 http://dx.doi.org/10.1038/s41467-017-00459-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shibata, Tomonori
Fujita, Yoshihiko
Ohno, Hirohisa
Suzuki, Yuki
Hayashi, Karin
Komatsu, Kaoru R.
Kawasaki, Shunsuke
Hidaka, Kumi
Yonehara, Shin
Sugiyama, Hiroshi
Endo, Masayuki
Saito, Hirohide
Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate
title Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate
title_full Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate
title_fullStr Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate
title_full_unstemmed Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate
title_short Protein-driven RNA nanostructured devices that function in vitro and control mammalian cell fate
title_sort protein-driven rna nanostructured devices that function in vitro and control mammalian cell fate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599586/
https://www.ncbi.nlm.nih.gov/pubmed/28912471
http://dx.doi.org/10.1038/s41467-017-00459-x
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