首页|冠状病毒主蛋白酶小分子有机硒化合物抑制剂筛选

冠状病毒主蛋白酶小分子有机硒化合物抑制剂筛选

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[目的]基于荧光共振能量转移技术(FRET)筛选抑制冠状病毒主蛋白酶(Mpro)活性的小分子有机硒化合物。[方法]将两种冠状病毒Mpro蛋白在大肠杆菌(Escherichia coli)BL21(DE3)中表达并纯化;基于FRET确认Mpro蛋白的体外活性并对13种小分子有机硒化合物进行筛选;进一步用MTT法测定有效化合物的细胞毒性;最后利用计算机软件AutoDock 4。2。6对有效化合物和两种冠状病毒Mpro进行分子对接分析。[结果]成功表达纯化出具有酶活性的两种Mpro蛋白;筛选发现11种化合物对两种Mpro均具有抑制效果，其中SLL-1A-46的抑制效果最显著，其对两种Mpro的酶活半抑制浓度(IC50)分别为:23。95 µmol/L(MERS-CoV)、24。97 μmol/L(SARS-CoV);细胞毒性检测结果显示SLL-1A-46 对三种细胞的半数毒性浓度(CC50)分别为 75。41 µmol/L(Vero E6)、39。96 µmol/L(A549)和 65。06μmol/L(293T);分子对接结果提示SLL-1A-46与两种Mpro活性位点处的结合能分别为-8。26 kcal/mol(MERS-CoV)和-8。37 kcal/mol(SARS-CoV)。[结论]初步筛选到11种抑制两种冠状病毒Mpro酶活性的小分子有机硒化合物，SLL-1A-46具有作为广谱冠状病毒Mpro抑制剂的潜力，其与两种Mpro的结合特点为广谱冠状病毒Mpro抑制剂的药物设计提供线索。
Screening of small-molecule organoselenium compounds inhibitors for the main protease of coronavirus
[Objective]To Screen of small molecule organic selenium compounds that inhibit the activity of coronavirus main protease(Mpro)based on fluorescence resonance energy transfer technology(FRET).[Method]Two types of coronavirus Mpro proteins were expressed in Escherichia coli BL21(DE3)and purified.The activity of Mpro protein was confirmed in vitro based on FRET and 13 small molecule organic selenium compounds were screened out.Further cytotoxicity of effective compounds was determined using the MIT method.Finally,molecular docking analysis was performed on the effective compounds and three types of coronavirus Mproby computer software AutoDock 4.2.6.[Result]Two types of Mpro proteins with enzymatic activity were successfully expressed and purified.Eleven compounds were found to have inhibitory effects on all two Mpro,in which SLL-1A-46 exerted the most significant inhibitory effects.The enzyme activity half maximal inhibitory concentration(IC50)of SLL-1A-46 on the two Mpro was 23.95 μmol/L for MERS-CoV,24.97 μmol/L for SARS-CoV respectively.The cytotoxicity test results shown that the median cytotoxic concentration(CC50)of SLL-1A-46 on two types of cells was 75.41 μmol/L for Ve-ro E6,39.96 μmol/L for A549,65.06 μmol/L for 293T respectively.The molecular docking results indicated that the bonding of SLL-1A-46 in two Mpro active sites is-8.26 kcal/mol for MERS CoV,and-8.37 kcal/mol for SARS-CoV respective-ly.[Conclusion]This study preliminarily screens 11 small-molecule organoselenium compounds that inhibit the activity of coronavirus Mpro.SLL-1A-46 has potential as a broad-spectrum coronavirus Mpro inhibitor.Its binding characteristics with two Mpro can provide clues for the drug design of broad-spectrum coronavirus Mpro inhibitors.

coronavirusMERS-CoVSARS-CoVmain proteaseprokaryotic expressionsmall-molecule organoselenium compoundsinhibitorsmolecular docking

孙攀、贺贤然、王承海、李卫玲、孙宾莲、张泽华、乔嘉璐

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江汉大学医学部,武汉生物医学研究院,湖北武汉 430056

冠状病毒 MERS-CoV SARS-CoV 主蛋白酶 原核表达 小分子有机硒化合物 抑制剂 分子对接

国家自然科学基金项目国家自然科学基金项目武汉市高校产学研项目江汉大学科研项目(中青年拔尖人才培养)江汉大学科研项目(湖北省自然基金创新群体)江汉大学科研项目(四新学科专项)

3167016732100131CXY20220408190006062100352022SXZX28

2024

10.16519/j.cnki.1004-311x.2024.03.0043

生物技术
黑龙江省微生物学会 黑龙江省生物工程学会 黑龙江省科学院微生物研究所

生物技术

CSTPCD
影响因子：0.611
ISSN：1004-311X
年,卷(期)：2024.34(3)