化学
核酸
生物传感器
分子信标
阿尔戈瑙特
DNA
滚动圆复制
数字聚合酶链反应
计算生物学
寡核苷酸
聚合酶链反应
生物化学
聚合酶
核糖核酸
基因
RNA干扰
生物
作者
Zhipan Wang,Feng Niu,Yanan Zhou,Xinrui Cheng,Cuiyun Zhou,Aimin Ma,Qinyu Wang,Yingjun Li,Yiping Chen
标识
DOI:10.1021/acs.analchem.3c04426
摘要
Detection of nucleic acids from a single multiplexed and amplification-free test is critical for ensuring food safety, clinical diagnostics, and environmental monitoring. In this study, we introduced a mesophilic Argonaute protein from Clostridium butyricum (CbAgo), which exhibits nucleic acid endonuclease activity, to achieve a programmable, amplification-free system (PASS) for rapid nucleic acid quantification at ambient temperatures in one pot. By using CbAgo-mediated binding with specific guide DNA (gDNA) and subsequent targeted cleavage of wild-type target DNAs complementary to gDNA, PASS can detect multiple foodborne pathogen DNA (<102 CFU/mL) simultaneously. The fluorescence signals were then transferred to polydisperse emulsions and analyzed by using deep learning. This simplifies the process and increases the suitability of polydisperse emulsions compared to traditional digital PCR, which requires homogeneous droplets for accurate detection. We believe that PASS has the potential to become a next-generation point-of-care digital nucleic acid detection method.
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