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Chimeric crRNA improves CRISPR-Cas12a specificity in the N501Y mutation detection of Alpha, Beta, Gamma, and Mu variants of SARS-CoV-2.

Jun YangNilakshi BaruaMd Nannur RahmanNorman LoTsz Fung TsangXiao YangPaul Kay Sheung ChanLi ZhangMargaret Ip
Published in: PloS one (2021)
Many CRISPR/Cas platforms have been established for the detection of SARS-CoV-2. But the detection platform of the variants of SARS-CoV-2 is scarce because its specificity is very challenging to achieve for those with only one or a few nucleotide(s) differences. Here, we report for the first time that chimeric crRNA could be critical in enhancing the specificity of CRISPR-Cas12a detecting of N501Y, which is shared by Alpha, Beta, Gamma, and Mu variants of SARS-CoV-2 without compromising its sensitivity. This strategy could also be applied to detect other SARS-CoV-2 variants that differ only one or a few nucleotide(s) differences.
Keyphrases
  • sars cov
  • crispr cas
  • genome editing
  • respiratory syndrome coronavirus
  • copy number
  • loop mediated isothermal amplification
  • cell therapy
  • label free
  • real time pcr
  • gene expression
  • single cell
  • sensitive detection