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Amplification-free RNA detection with CRISPR–Cas13

CRISPR-based nucleic-acid detection is an emerging technology for molecular diagnostics. However, these methods generally require several hours and could cause amplification errors, due to the pre-amplification of target nucleic acids to enhance the detection sensitivity. Here, we developed a platfo...

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Autores principales: Shinoda, Hajime, Taguchi, Yuya, Nakagawa, Ryoya, Makino, Asami, Okazaki, Sae, Nakano, Masahiro, Muramoto, Yukiko, Takahashi, Chiharu, Takahashi, Ikuko, Ando, Jun, Noda, Takeshi, Nureki, Osamu, Nishimasu, Hiroshi, Watanabe, Rikiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055673/
https://www.ncbi.nlm.nih.gov/pubmed/33875803
http://dx.doi.org/10.1038/s42003-021-02001-8
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author Shinoda, Hajime
Taguchi, Yuya
Nakagawa, Ryoya
Makino, Asami
Okazaki, Sae
Nakano, Masahiro
Muramoto, Yukiko
Takahashi, Chiharu
Takahashi, Ikuko
Ando, Jun
Noda, Takeshi
Nureki, Osamu
Nishimasu, Hiroshi
Watanabe, Rikiya
author_facet Shinoda, Hajime
Taguchi, Yuya
Nakagawa, Ryoya
Makino, Asami
Okazaki, Sae
Nakano, Masahiro
Muramoto, Yukiko
Takahashi, Chiharu
Takahashi, Ikuko
Ando, Jun
Noda, Takeshi
Nureki, Osamu
Nishimasu, Hiroshi
Watanabe, Rikiya
author_sort Shinoda, Hajime
collection PubMed
description CRISPR-based nucleic-acid detection is an emerging technology for molecular diagnostics. However, these methods generally require several hours and could cause amplification errors, due to the pre-amplification of target nucleic acids to enhance the detection sensitivity. Here, we developed a platform that allows “CRISPR-based amplification-free digital RNA detection (SATORI)”, by combining CRISPR-Cas13-based RNA detection and microchamber-array technologies. SATORI detected single-stranded RNA targets with maximal sensitivity of ~10 fM in <5 min, with high specificity. Furthermore, the simultaneous use of multiple different guide RNAs enhanced the sensitivity, thereby enabling the detection of the SARS-CoV-2 N-gene RNA at ~5 fM levels. Therefore, we hope SATORI will serve as a powerful class of accurate and rapid diagnostics.
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spelling pubmed-80556732021-05-05 Amplification-free RNA detection with CRISPR–Cas13 Shinoda, Hajime Taguchi, Yuya Nakagawa, Ryoya Makino, Asami Okazaki, Sae Nakano, Masahiro Muramoto, Yukiko Takahashi, Chiharu Takahashi, Ikuko Ando, Jun Noda, Takeshi Nureki, Osamu Nishimasu, Hiroshi Watanabe, Rikiya Commun Biol Article CRISPR-based nucleic-acid detection is an emerging technology for molecular diagnostics. However, these methods generally require several hours and could cause amplification errors, due to the pre-amplification of target nucleic acids to enhance the detection sensitivity. Here, we developed a platform that allows “CRISPR-based amplification-free digital RNA detection (SATORI)”, by combining CRISPR-Cas13-based RNA detection and microchamber-array technologies. SATORI detected single-stranded RNA targets with maximal sensitivity of ~10 fM in <5 min, with high specificity. Furthermore, the simultaneous use of multiple different guide RNAs enhanced the sensitivity, thereby enabling the detection of the SARS-CoV-2 N-gene RNA at ~5 fM levels. Therefore, we hope SATORI will serve as a powerful class of accurate and rapid diagnostics. Nature Publishing Group UK 2021-04-19 /pmc/articles/PMC8055673/ /pubmed/33875803 http://dx.doi.org/10.1038/s42003-021-02001-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shinoda, Hajime
Taguchi, Yuya
Nakagawa, Ryoya
Makino, Asami
Okazaki, Sae
Nakano, Masahiro
Muramoto, Yukiko
Takahashi, Chiharu
Takahashi, Ikuko
Ando, Jun
Noda, Takeshi
Nureki, Osamu
Nishimasu, Hiroshi
Watanabe, Rikiya
Amplification-free RNA detection with CRISPR–Cas13
title Amplification-free RNA detection with CRISPR–Cas13
title_full Amplification-free RNA detection with CRISPR–Cas13
title_fullStr Amplification-free RNA detection with CRISPR–Cas13
title_full_unstemmed Amplification-free RNA detection with CRISPR–Cas13
title_short Amplification-free RNA detection with CRISPR–Cas13
title_sort amplification-free rna detection with crispr–cas13
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055673/
https://www.ncbi.nlm.nih.gov/pubmed/33875803
http://dx.doi.org/10.1038/s42003-021-02001-8
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