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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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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. |
format | Online Article Text |
id | pubmed-5599586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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