Heparin Specifically Inhibits CRISPR/Cas12 Activation, Enabling Ultrasensitive Heparin Detection and Gene Editing Regulation.
Min CaoXinlan BianZhirun JiMuhammad SohailFuming ZhangRobert J LinhardtBingzhi LiXing ZhangPublished in: Analytical chemistry (2024)
Heparin is a highly sulfated linear glycosaminoglycan that is used as an anticoagulant to prevent and treat thrombotic diseases. Herein, we find that heparin specifically inhibits the activation of the Cas12 protein through the competitive binding of heparin and crRNA to Cas12. Studies illustrate that heparin's high molecular weight and strong negative charge are critical parameters for its inhibitory effect. This unexpected finding was engineered for the detection of heparin, affording a low detection limit of 0.36 ng/mL for fluorometric quantification. We further developed a rapid lateral flow-based system named HepaStrip ( hepa rin strip ), allowing heparin monitoring in clinical samples within 20 min. Finally, in vivo investigations revealed that heparin can regulate gene editing with the clusters of the regularly spaced short palindromic repeat (CRISPR)/Cas12 system in Escherichia coli . Heparin blocks the formation of Cas12-crRNA ribonucleoprotein, allowing the application of CRISPR for rapid and field-deployable detection of heparin and unleashing the potential use of heparin in future anti-CRISPR applications.
Keyphrases
- crispr cas
- venous thromboembolism
- genome editing
- growth factor
- loop mediated isothermal amplification
- escherichia coli
- gene expression
- dna methylation
- label free
- pseudomonas aeruginosa
- small molecule
- mass spectrometry
- multidrug resistant
- real time pcr
- transcription factor
- binding protein
- sensitive detection
- neural network
- klebsiella pneumoniae