| Literature DB >> 31532637 |
Linxian Li1,2,3, Shiyuan Li4, Na Wu1,2,5, Jiacheng Wu5, Gang Wang3, Guoping Zhao2,6, Jin Wang7.
Abstract
The next-generation CRISPR-based molecular diagnostics has the merits of rapidness, accuracy, and portability. We discovered the Cas12a trans-cleavage activity against collateral single-stranded DNA (ssDNA) and employed the activity to develop a rapid nucleic acid detection system, namely HOLMES (one-hour low-cost multipurpose highly efficient system). Here, with the employment of thermophilic CRISPR-Cas12b, we create HOLMESv2 for four different applications: (1) specifically discriminating single nucleotide polymorphism (SNP); (2) simply detecting virus RNA, human cell mRNA and circular RNA; (3) conveniently quantitating target nucleic acids with a one-step system combined with LAMP amplification in a constant temperature, thus avoiding cross-contamination; (4) accurately quantitating target DNA methylation degree with the combination of Cas12b detection and bisulfite treatment. These results highlight the potential of HOLMESv2 as a promising platform for both molecular diagnostics and epigenetics applications.Entities:
Keywords: CRISPR; Cas12b; DNA methylation quantitation; HOLMES; nucleic acid detection
Mesh:
Substances:
Year: 2019 PMID: 31532637 DOI: 10.1021/acssynbio.9b00209
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110