蛋白酵素
DNA
肽
化学
蛋白酶
生物化学
多路复用
分子生物学
组织蛋白酶
酶
生物
生物信息学
作者
Dylan Snider,Mackenzie Coffin,Brian Armijo,Ryan Khetan,Mark Duchow,Anna Capasso,Devleena Samanta
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-04-13
卷期号:64 (25): e202500649-e202500649
被引量:9
标识
DOI:10.1002/anie.202500649
摘要
We introduce a new class of chemical probes for activity-based sensing of proteases, termed cleavable, locked initiator probes (CLIPs). CLIPs contain a protease-cleavable peptide linked between two programmable DNA strands-an "initiator" DNA and a shorter "blocking" DNA. These DNA sequences are designed to hybridize, creating a "locked" hairpin-like structure. Upon proteolytic cleavage, the initiator strand is released, triggering the activation of CRISPR-Cas12a enzymes and producing an amplified fluorescence response. CLIPs generate more than 20-fold turn-on signals at room temperature (25 °C), significantly outperforming commercial probes by yielding ∼40-fold lower limits of detection (LOD) at 100-fold lower concentrations. Their versatility enables the detection of various disease-relevant proteases-including the SARS-CoV-2 main protease, caspase-3, matrix metalloproteinase-7, and cathepsin B-simply by altering the peptide sequence. Importantly, CLIPs detect cathepsin B in four different colorectal cancer cell lines, highlighting their clinical potential. Taken together, the sensitivity (LOD: ∼88 pM), selectivity, and rapid assay time (down to 35 min), combined with the ability to operate in complex biological media with minimal sample preparation, position CLIPs as powerful chemical tools for activity-based sensing of functional enzymes.
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