化学
核酸
计算生物学
反式激活crRNA
重组酶聚合酶扩增
酰化
核糖核酸
聚合酶
清脆的
基因
灵敏度(控制系统)
重组酶
纳米技术
核酸检测
组合化学
鉴定(生物学)
DNA
生物系统
作者
Jinlian Du,X. Pu,Tongyan Yuan,Fang Peng,Jingjing Hu,Han Zhe Li,Bojie Chen,Jiaming Luo,Sheng Li,Yuling Teng,Xinyue Zhu,Weiming Chen,Qingqing Xie,Ling Jiang,Erhu Xiong,Ronghua Yang
标识
DOI:10.1021/acs.analchem.5c05769
摘要
Precise spatiotemporal control of CRISPR activity is central to both accurate gene editing and sensitive molecular diagnostics. However, current regulatory strategies are often sequence-specific, labor-intensive, and difficult to generalize. Here, we report a minimalist plug-and-play tactic: acylation of the repeat region (rRNA) of a split crRNA with photolabile groups. Because the modification is introduced post-synthesis and is independent of the spacer region (sRNA), every rRNA, regardless of its target sequence, can be activated by light irradiation alone, entirely eliminating the need for redesign or reoptimization. Integrating the photo-initiated CRISPR-Cas12a system with recombinase polymerase amplification into a one-pot format yields an upgraded platform, named POIROTv2 (PhotO-Initiated CRISPR-Cas12a system for Robust One-pot Testing, version 2). POIROTv2 achieves a 100-fold sensitivity gain over conventional always-on Cas12a-based one-pot assays and matches the analytical performance of a two-step assay while remaining a more streamlined and potentially faster detection process and avoiding the risk of aerosol contamination. In clinical validation with HCMV- and EBV-suspected samples, POIROTv2 delivered diagnostic accuracy statistically indistinguishable from that of gold-standard qPCR, highlighting its potential for robust and sensitive molecular diagnostics. Overall, the strategy opens up exciting possibilities for applications in infectious virus diagnostics and has broad prospects in the field of spatiotemporally controllable gene editing.
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