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February 14, 2026Nature Communications0 citationsOpen Access

PRICE: direct and robust detection of microRNAs at single-nucleotide resolution

BWBuhua WangSZShuai ZhouXZXi Zhang

Key Points

  • The research aims to develop a method for accurate detection of single nucleotide variations in microRNAs.
  • Developed a PNA-mediated CRISPR/Cas13a system called PRICE
  • Utilized PNA blockers to inhibit non-target miRNAs
  • Applied the system to various samples like serum and tissues
  • Designed a panel of PNAs specific to SNVs
  • Achieved detection sensitivity down to ~10 fM
  • Successfully distinguished between target and non-target miRNAs
  • Demonstrated the potential for applications in cancer diagnosis and prognosis

Abstract

Abstract Accurate single-nucleotide discrimination of miRNA is clinically vital because small sequence variations can have significant phenotypic and clinical consequences, yet existing techniques can only detect single nucleotide variations (SNVs) at specific loci. Here, we present a generalized peptide nucleic acid ( P NA) mediated C RI SPR/ C as13a syst e m (PRICE), enabling detection of SNVs in miRNA sequence without sacrificing the sensitivity. PRICE utilizes PNA blockers fully complementary to non-target miRNAs (e.g., miRNAs containing SNVs at loci of no interest) but not to the target miRNA. These blockers selectively hybridize with and inhibit non-target sequences in samples (serum, cells, or tissues). Only the unhybridized target miRNA then binds to crRNA within the Cas13a complex, activating Cas13a to cleave a fluorescent reporter-quencher linker, generating a detectable signal (~10 fM limit). By designing a panel of PNAs against SNVs, PRICE provides a versatile, amplification-free platform for precise miRNA analysis, advancing cancer diagnosis, prognosis, and biology.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/699011812ccff479cfe583e0https://doi.org/10.1038/s41467-026-69181-x
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