清脆的
核酸
基因组编辑
计算生物学
纳米技术
病毒
生物
病毒学
材料科学
遗传学
基因
作者
Huijie Li,Jie Yang,Guangfu Wu,Zhengyan Weng,Yang Song,Yuxuan Zhang,Jeffrey A. Vanegas,Lori Avery,Zan Gao,He Sun,Yupeng Chen,Kevin D. Dieckhaus,Xue Gao,Yi Zhang
标识
DOI:10.1002/anie.202203826
摘要
The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) systems have recently received notable attention for their applications in nucleic acid detection. Despite many attempts, the majority of current CRISPR-based biosensors in infectious respiratory disease diagnostic applications still require target preamplifications. This study reports a new biosensor for amplification-free nucleic acid detection via harnessing the trans-cleavage mechanism of Cas13a and ultrasensitive graphene field-effect transistors (gFETs). CRISPR Cas13a-gFET achieves the detection of SARS-CoV-2 and respiratory syncytial virus (RSV) genome down to 1 attomolar without target preamplifications. Additionally, we validate the detection performance using clinical SARS-CoV-2 samples, including those with low viral loads (Ct value >30). Overall, these findings establish our CRISPR Cas13a-gFET among the most sensitive amplification-free nucleic acid diagnostic platforms to date.
科研通智能强力驱动
Strongly Powered by AbleSci AI