反式激活crRNA
清脆的
周转时间
检测点注意事项
注意事项
计算生物学
核糖核酸
材料科学
病毒学
纳米技术
计算机科学
生物
医学
基因组编辑
基因
遗传学
免疫学
病理
操作系统
作者
Wanting Zeng,Wan‐Ping Chen,Yang Liu,Ting Zhang,Chao Zhai,Wenqiang Li,Longyu Wang,Cheng Zhang,Qili Zeng,Fei Wang,Lixin Ma
标识
DOI:10.1016/j.bios.2024.116400
摘要
CRISPR based nucleic acid detection technology provides a deployable approach to point of care testing. While, there remain challenges limiting its practical applications, such as the need for pre-amplification and the long turnaround time. Here, we present a self-cascade signal amplification method with LwaCas13a and an artificially designed "U" rich RNA of stem-loop structure (URH) for pre-amplification-free ultra-fast and ultra-sensitive point-of-care testing (PASSPORT). The PASSPORT system contains: URH, crRNA targeted the URH, crRNA targeted the interesting RNA, fluorescent RNA reporter and LwaCas13a. The assay realized the detection of 100 copies/mL, within 5 min. The PASSPORT platform was further adopted for the detection of marker gene from SASR-CoV-2 and Severe fever with thrombocytopenia syndrome virus (SFTSV), respectively, and 100% accuracy for the analysis of clinical specimens (100 SASR-CoV-2 specimens and 16 SFTSV specimens) was obtained. Integrated with a lateral flow assay device, this assay could provide an alternative platform for the development of point of care testing (POCT) biosensors. PASSPORT has the potential to enable sensitive, specific, user-friendly, rapid, affordable, equipment-free and point-of-care testing for the purpose of large-scale screening and in case of epidemic outbreak.
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