Peptides targeting dengue viral nonstructural protein 1 inhibit dengue virus production

被引:21
|
作者
Songprakhon, Pucharee [1 ]
Thaingtamtanha, Thanawat [2 ,10 ]
Limjindaporn, Thawornchai [3 ]
Puttikhunt, Chunya [4 ,5 ,6 ]
Srisawat, Chatchawan [7 ]
Luangaram, Prasit [4 ,5 ,6 ]
Dechtawewat, Thanyaporn [1 ]
Uthaipibull, Chairat [8 ]
Thongsima, Sissades [9 ]
Yenchitsomanus, Pa-thai [1 ]
Malasit, Prida [4 ,5 ,6 ]
Noisakran, Sansanee [4 ,5 ,6 ]
机构
[1] Mahidol Univ, Siriraj Hosp, Fac Med, Div Mol Med,Res Dept, Bangkok, Thailand
[2] Rangsit Univ, Fac Pharm, Pathum Thani, Thailand
[3] Mahidol Univ, Fac Med, Dept Anat, Siriraj Hosp, Bangkok, Thailand
[4] Natl Sci & Technol Dev Agcy, Natl Ctr Genet Engn & Biotechnol, Mol Biol Dengue & Flaviviruses Res Team, Med Mol Biotechnol Res Grp, Bangkok, Thailand
[5] Mahidol Univ, Div Dengue Hemorrhag Fever Res, Res Dept, Fac Med,Siriraj Hosp, Bangkok, Thailand
[6] Mahidol Univ, Fac Med, Siriraj Ctr Res Excellence Dengue & Emerging Path, Siriraj Hosp, Bangkok, Thailand
[7] Mahidol Univ, Dept Biochem, Fac Med, Siriraj Hosp, Bangkok, Thailand
[8] Natl Sci & Technol Dev Agcy, Prot Ligand Engn & Mol Biol Res Team, Med Mol Biotechnol Res Grp, Natl Ctr Genet Engn & Biotechnol, Pathum Thani, Thailand
[9] Natl Sci & Technol Dev Agcy, Natl Biobank Thailand, Pathum Thani, Thailand
[10] Univ Siegen, Dept Chem & Biol, Siegen, Germany
关键词
NS1; PROTEIN; CYCLIC PEPTIDE; MOLECULAR-DYNAMICS; GLYCOPROTEIN NS1; TRANSLATION; REPLICATION; DISCOVERY; INTERACTS; BINDING; REGION;
D O I
10.1038/s41598-020-69515-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Viruses manipulate the life cycle in host cells via the use of viral properties and host machineries. Development of antiviral peptides against dengue virus (DENV) infection has previously been concentrated on blocking the actions of viral structural proteins and enzymes in virus entry and viral RNA processing in host cells. In this study, we proposed DENV NS1, which is a multifunctional non-structural protein indispensable for virus production, as a new target for inhibition of DENV infection by specific peptides. We performed biopanning assays using a phage-displayed peptide library and identified 11 different sequences of 12-mer peptides binding to DENV NS1. In silico analyses of peptide-protein interactions revealed 4 peptides most likely to bind to DENV NS1 at specific positions and their association was analysed by surface plasmon resonance. Treatment of Huh7 cells with these 4 peptides conjugated with N-terminal fluorescent tag and C-terminal cell penetrating tag at varying time-of-addition post-DENV infection could inhibit the production of DENV-2 in a time- and dose-dependent manner. The inhibitory effects of the peptides were also observed in other virus serotypes (DENV-1 and DENV-4), but not in DENV-3. These findings indicate the potential application of peptides targeting DENV NS1 as antiviral agents against DENV infection.
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页数:16
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