重组酶聚合酶扩增
核酸
多路复用
清脆的
计算生物学
核酸扩增试验
生物
分子信标
聚合酶
多重聚合酶链反应
微流控
聚合酶链反应
分子生物学
DNA
环介导等温扩增
病毒学
遗传学
基因
纳米技术
寡核苷酸
材料科学
沙眼衣原体
作者
Zhichen Xu,Dongjuan Chen,Tao Li,Jiayu Yan,Jiang Zhu,Ting He,Rui Hu,Ying Li,Yunhuang Yang,Maili Liu
标识
DOI:10.1038/s41467-022-34086-y
摘要
Abstract Fast, inexpensive, and multiplexed detection of multiple nucleic acids is of great importance to human health, yet it still represents a significant challenge. Herein, we propose a nucleic acid testing platform, named MiCaR, which couples a mi crofluidic device with CRISPR- C as12a a nd multiplex r ecombinase polymerase amplification. With only one fluorescence probe, MiCaR can simultaneously test up to 30 nucleic acid targets through microfluidic space coding. The detection limit achieves 0.26 attomole, and the multiplexed assay takes only 40 min. We demonstrate the utility of MiCaR by efficiently detecting the nine HPV subtypes targeted by the 9-valent HPV vaccine, showing a sensitivity of 97.8% and specificity of 98.1% in the testing of 100 patient samples at risk for HPV infection. Additionally, we also show the generalizability of our approach by successfully testing eight of the most clinically relevant respiratory viruses. We anticipate this effective, undecorated and versatile platform to be widely used in multiplexed nucleic acid detection.
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