CoHIT: a one-pot ultrasensitive ERA-CRISPR system for detecting multiple same-site indels.
Yin LiuXinyi LiuDongyi WeiLu DangXiaoran XuShisheng HuangLiwen LiSanyun WuJinxian WuXiaoyan LiuWenjun SunWanyu TaoYongchang WeiXing-Xu HuangKui LiXinjie WangFuling ZhouPublished in: Nature communications (2024)
Genetic testing is crucial for precision cancer medicine. However, detecting multiple same-site insertions or deletions (indels) is challenging. Here, we introduce CoHIT (Cas12a-based One-for-all High-speed Isothermal Test), a one-pot CRISPR-based assay for indel detection. Leveraging an engineered AsCas12a protein variant with high mismatch tolerance and broad PAM scope, CoHIT can use a single crRNA to detect multiple NPM1 gene c.863_864 4-bp insertions in acute myeloid leukemia (AML). After optimizing multiple parameters, CoHIT achieves a detection limit of 0.01% and rapid results within 30 minutes, without wild-type cross-reactivity. It successfully identifies NPM1 mutations in 30 out of 108 AML patients and demonstrates potential in monitoring minimal residual disease (MRD) through continuous sample analysis from three patients. The CoHIT method is also competent for detecting indels of KIT, BRAF, and EGFR genes. Integration with lateral flow test strips and microfluidic chips highlights CoHIT's adaptability and multiplexing capability, promising significant advancements in clinical cancer diagnostics.
Keyphrases
- genome wide
- acute myeloid leukemia
- end stage renal disease
- crispr cas
- high speed
- ejection fraction
- newly diagnosed
- genome editing
- prognostic factors
- wild type
- peritoneal dialysis
- papillary thyroid
- label free
- gene expression
- loop mediated isothermal amplification
- patient reported outcomes
- squamous cell carcinoma
- gold nanoparticles
- mass spectrometry
- quantum dots
- single cell
- high resolution
- risk assessment
- tyrosine kinase
- binding protein
- lymph node metastasis
- small molecule
- solid phase extraction