| Literature DB >> 33875803 |
Hajime Shinoda1, Yuya Taguchi1, Ryoya Nakagawa2, Asami Makino1, Sae Okazaki3, Masahiro Nakano4, Yukiko Muramoto4, Chiharu Takahashi1, Ikuko Takahashi1, Jun Ando1, Takeshi Noda4, Osamu Nureki5, Hiroshi Nishimasu6, Rikiya Watanabe7.
Abstract
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.Entities:
Year: 2021 PMID: 33875803 DOI: 10.1038/s42003-021-02001-8
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642