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作 者:韩冰 张岱[2] 陈小菲[3] 李伟霞[3,4] 吴娅丽 王晓艳[3] 张辉[3] 汪彬 蒋雪松[2] 贾金浩 纪秋如 孟高全 孟伟亭 王炜[5] 唐进法[3,4] HAN Bing;ZHANG Dai;CHEN Xiaofei;LI Weixia;WU Yali;WANG Xiaoyan;ZHANG Hui;WANG Bing;JIANG Xuesong;JIA Jinhao;JI Qiuru;MENG Gaoquan;MENG Weiting;WANG Wei;TANG Jinfa(School of Pharmacy,Henan University of Chinese Medicine,Zhengzhou 450046;Department of Laboratory Medicine,The First Affiliated Hospital of Henan University of Chinese Medicine,Zhengzhou 450046;Henan Province Engineering Research Center for Clinical Application,Evaluation and Transformation of Traditional Chinese Medicine,Henan Province Engineering Research Center of Safety Evaluation and Risk Management of Traditional Chinese Medicine,Henan Provincial Key Laboratory for Clinical Pharmacy of Traditional Chinese Medicine,The First Affiliated Hospital of Henan University of Chinese Medicine,Zhengzhou 450000;Collaborative Innovation Center for Chinese Medicine and Respiratory Diseases Co-constructed by Henan Province&Education Ministry of P.R.China,Henan University of Chinese Medicine,Zhengzhou 450046;Department of Infection Control,The First Affiliated Hospital of Henan University of Chinese Medicine,Zhengzhou 450000)
机构地区:[1]河南中医药大学药学院,郑州450046 [2]河南中医药大学第一附属医院检验科,郑州450046 [3]河南中医药大学第一附属医院,河南省中药临床应用、评价与转化工程研究中心,河南省中药安全评价与风险防控工程研究中心,河南省中药临床药学中医药重点实验室,郑州450000 [4]河南中医药大学,呼吸疾病中医药防治省部共建协同创新中心,郑州450046 [5]河南中医药大学第一附属医院感染控制科,郑州450000
出 处:《中药药理与临床》2024年第6期38-44,共7页Pharmacology and Clinics of Chinese Materia Medica
基 金:河南省中医药科学研究专项课题(编号:2023ZY2042);河南省高校科技创新团队(编号:23IRTSTHN026);2022财政专项-中医药传承与创新人才工程(仲景工程);2023年财政专项-中药创新能力提升项目-医疗机构中药制剂创新能力提升。
摘 要:目的:利用荧光共振能量转移(Fluorescence resonance energy transfer,FRET)技术构建新冠病毒主蛋白酶(SARS-CoV-2 Mpro)中药抑制剂的体外筛选方法。方法:构建Mpro及筛选探针原核表达的工程质粒pGEX-4T-1-Mpro、pET-28a(+)-Ls-mK。使用荧光探针Ls-mK检测Mpro的生物活性及酶动力学参数,并对筛选条件进行优化。采用阳性药物GC-376及阴性对照PLpro(Papain-like protease)和TEV酶(Tobacco Etch Virus Proteinase)评价荧光探针Ls-mK的特异性及检测能力与商业化探针的差异。根据所构建的筛选体系考察五种中药制剂筛选热毒宁注射液、血必净注射液、抗病毒口服液和蒲地蓝口服液对Mpro的抑制能力。结果:本研究成功构建原核表达的工程质粒并获得纯度为90%左右的重组蛋白荧光探针Ls-mK及Mpro。荧光探针Ls-mK可成功产生FRET现象并具有良好的特异性。Mpro具有良好的生物活性。本研究所构建的筛选体系具有与商业化探针相同的检测能力,对五种中药制剂考察发现仅喜炎平注射液对Mpro具有良好的抑制活性,其IC_(50)值为(3.32±0.03)mg/mL。结论:本研究成功构建基于荧光蛋白SARS-CoV-2 Mpro的简便、灵敏和低成本的筛选体系,为新冠病毒主蛋白酶抑制剂的筛选与发现奠定了实验基础。Objective:To construct an in vitro screening system of Chinese medicine inhibitors of SARS-CoV-2 Mpro by fluorescence resonance energy transfer(FRET)technology.Methods:The engineering plasmids pGEX-4T-1-Mpro and pET-28a(+)-Ls-mK were constructed.The biological activity and enzyme kinetic parameters of Mpro were determined by the fluorescent probe Ls-mK,and the screening conditions were optimized.The differences between fluorescent probe Ls-mK and commercial probe in specificity and detection ability were evaluated by the positive drug GC-376 and the negative control papain-like protease(PLpro)and tobacco etch virus(TEV)protease.According to the constructed screening system,the inhibitory ability of five Chinese medicine preparations against Mpro was investigated,including Reduning(热毒宁)Injection,Xuebijing(血必净)Injection,Antiviral Oral Liquid and Pudilan(蒲地蓝)Oral Liquid.Results:The engineering plasmid expressed in prokaryotes was successfully constructed,and the recombinant protein fluorescent probes Ls-mK and Mpro with a purity of about 90%were obtained.The fluorescent probe Ls-mK produced FRET phenomenon and presented good specificity.Mpro had good biological activity.The screening system constructed in this paper specifically had the same detection ability as commercial probes.It was found that only Xiyanping Injection inhibited Mpro,with an IC_(50) value of 3.32±0.03 mg/mL.Conclusion:This paper successfully constructed a simple,sensitive and low-cost screening system based on SARS-CoV-2 Mpro,which laid an experimental foundation for the screening and discovery of SARS-CoV-2 Mpro inhibitors.
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