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
- acute myeloid leukemia
- genome wide
- end stage renal disease
- newly diagnosed
- high speed
- ejection fraction
- chronic kidney disease
- wild type
- genome editing
- papillary thyroid
- prognostic factors
- label free
- small cell lung cancer
- peritoneal dialysis
- gene expression
- high throughput
- squamous cell
- squamous cell carcinoma
- gold nanoparticles
- quantum dots
- dna methylation
- small molecule
- single cell
- circulating tumor cells
- real time pcr
- molecularly imprinted
- copy number
- childhood cancer
- acute lymphoblastic leukemia
- sensitive detection
- liquid chromatography
- genome wide identification
- nucleic acid