核酸
核酸酶
DNA
核酸法
核酸检测
化学
清脆的
计算生物学
核糖核酸
核酸热力学
核酸定量
生物化学
寡核苷酸
脱氧核酶
核苷酸
杂交探针
点突变
生物
基因
肽核酸
纳米技术
锁核酸
分子生物学
作者
Hang Gao,Yuting Shuai,Yiyi Zheng,Anan Xu,Zhaoxi Han,Dini Ma,Zixin Deng,Xinyi He,Guang Liu
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2025-10-28
卷期号:10 (11): 8481-8488
被引量:2
标识
DOI:10.1021/acssensors.5c01987
摘要
Nucleic acid detection plays an essential role in disease diagnosis and epidemic control. Traditional techniques face challenges such as time-consuming procedures and limited accuracy. Despite progress in programmable nuclease systems such as CRISPR and Argonaute, there has been relatively limited exploration of nucleic acid detection methods utilizing DNA modifications. We have previously developed SENSOR (sulfur DNA-mediated nucleic acid sensing platform) for rapid detection of single-stranded DNA (ssDNA) by employing phosphorothioate (PT) modification and sulfur binding domains (SBDs). Here we present SENSOR 2.0, which has been expanded to detect RNA at single-copy level sensitivity. In addition, using a Bubble-Probe design, SENSOR 2.0 is capable of distinguishing single nucleotide variations (SNVs). In 57 clinical Candida albicans samples, the azole drug-resistant point mutation in the ERG11 gene was successfully identified with SENSOR 2.0. These results establish SENSOR 2.0 as an innovative and highly effective technique for nucleic acid detection.
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