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摘要:
Lassa hemorrhagic fever,caused by Lassa mammarenavirus (LASV) infection,accumulates up to 5000 deaths every year.Currently,there is no vaccine available to combat this disease.In this study,a library of 200 bioactive compounds was virtually screened to study their drug-likeness with the capacity to block the α-dystroglycan (α-DG) receptor and prevent LASV influx.Following rigorous absorption,distribution,metabolism,and excretion(ADME) and quantitative structure-activity relationship (QSAR) profiling,molecular docking was conducted with the top ligands against the α-DG receptor.The compounds chrysin,reticuline,and 3-caffeoylshikimic acid emerged as the top three ligands in terms of binding affinity.Post-docking analysis revealed that interactions with Arg76,Asn224,Ser259,and Lys302 amino acid residues of the receptor protein were important for the optimum binding affinity of ligands.Molecular dynamics simulation was performed comprehensively to study the stability of the protein-ligand complexes.In-depth assessment of root-mean-square deviation (RMSD),root mean square fluctuation (RMSF),polar surface area (PSA),B-Factor,radius of gyration (Rg),solvent accessible surface area(SASA),and molecular surface area (MolSA) values of the protein-ligand complexes affirmed that the candidates with the best binding affinity formed the most stable protein-ligand complexes.To authenticate the potentialities of the ligands as target-specific drugs,an in vivo study is underway in real time as the continuation of the research.
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篇名 Target specificity of selective bioactive compounds in blocking α-dystroglycan receptor to suppress Lassa virus infection:an in silico approach
来源期刊 生物医学研究杂志(英文版) 学科 医学
关键词
年,卷(期) 2021,(6) 所属期刊栏目 Molecular Pharmacology
研究方向 页码范围 459-473
页数 15页 分类号 R966
字数 语种 英文
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生物医学研究杂志(英文版)
双月刊
1674-8301
32-1810/R
16开
南京市汉中路140号
1987
eng
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1328
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0
总被引数(次)
3140
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