Amplification-Free Detection of SARS-CoV-2 and Respiratory Syncytial Virus Using CRISPR Cas13a and Graphene Field-Effect Transistors.
Huijie LiJie YangGuangfu WuZhengyan WengYang SongYuxuan ZhangJeffrey A VanegasLori AveryZan GaoHe SunYupeng ChenKevin D DieckhausXue GaoYi ZhangPublished in: Angewandte Chemie (International ed. in English) (2022)
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.
Keyphrases
- nucleic acid
- crispr cas
- genome editing
- sars cov
- label free
- respiratory syncytial virus
- loop mediated isothermal amplification
- genome wide
- real time pcr
- respiratory syndrome coronavirus
- computed tomography
- emergency department
- sensitive detection
- artificial intelligence
- coronavirus disease
- mass spectrometry
- transcription factor
- machine learning
- high resolution
- magnetic resonance
- drug induced
- tandem mass spectrometry
- electronic health record
- contrast enhanced