小RNA
计算生物学
序列(生物学)
核酸
劈开
生物
复式(建筑)
计算机科学
肽核酸
互补序列
锁核酸
表型
反式激活crRNA
基因
生物信息学
基序列
遗传学
DNA
分辨率(逻辑)
HEK 293细胞
DNA测序
核苷酸
核酸序列
肽序列
癌症
鉴定(生物学)
系统生物学
作者
Buhua Wang,Shuai Zhou,Xi Zhang,Rui Wang,Shuo Huang,Anyi Li,Haowei He,Yalin Zhang,Yangdao Wei,Zhiqing Yang,Fengge Song,Xiangpeng Li,Xinyi Wan,Yi Shen,Chunxin Ma,Haimei Mao,Rodrigo Ledesma‐Amaro,D P Yin,Qingshan Wei,Ruijie Deng
标识
DOI:10.1038/s41467-026-69181-x
摘要
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 (PNA) mediated CRISPR/Cas13a system (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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