化学发光
化学
检出限
放射性检测
蛋白酶
病毒
2019年冠状病毒病(COVID-19)
基质(水族馆)
药物发现
体内
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
共价键
生物标志物
分子探针
组合化学
酶
计算生物学
色谱法
生物化学
病毒学
生物技术
有机化学
医学
DNA
海洋学
疾病
病理
人工智能
计算机科学
传染病(医学专业)
生物
地质学
作者
Suping Xia,En Liang,Lin Xu,Liyi Tan,Xiaowen Guo,Kui Cheng
标识
DOI:10.1021/acs.analchem.4c04774
摘要
In the postpandemic era, the emergence of "long COVID" from SARS-CoV-2 has brought ongoing negative impacts on individual health and society. The development of more efficient methods for drug screening and monitoring viral activity remains a critical need. The main protease (Mpro), due to its important role in the virus lifecycle, high conservation, and specificity, is considered an ideal biomarker for SARS-CoV-2. Herein, we have developed several chemiluminescence probes based on different substrates modified from covalent inhibitors targeted at Mpro. Among these, the best probe, MPCL-2, exhibits a rapid response (<20 min), an extremely low limit of detection (LoD; 0.11 nM), great selectivity, and chemical stability. After validating the probe's mechanism of action, MPCL-2 can also be used for real-time, in-situ imaging of enzymes in cells infected with the authentic virus and has the potential for real-time, in-situ Mpro imaging in vivo. Compared to other methods reported to date, the probe demonstrates superior performance and broader applicability, such as in drug screening or virus activity monitoring. Further, the unique design strategy for the substrate can be adopted to develop sensitive probes for other pathogens.
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