Computer-Aided Screening for Potential Coronavirus 3-Chymotrypsin-like Protease (3CLpro) Inhibitory Peptides from Putative Hemp Seed Trypsinized Peptidome

被引:7
|
作者
Prasertsuk, Kansate [1 ]
Prongfa, Kasidit [1 ]
Suttiwanich, Piyapach [1 ]
Harnkit, Nathaphat [2 ]
Sangkhawasi, Mattanun [3 ]
Promta, Pongsakorn [1 ]
Chumnanpuen, Pramote [4 ,5 ]
机构
[1] Pibulwitthayalai Sch, 777 Naraimaharach, Lopburi 15000, Thailand
[2] Minist Publ Hlth, Dept Med Sci, Med Plant Res Inst, Nonthaburi 11000, Thailand
[3] Chulalongkorn Univ, Fac Sci, Program Biotechnol, Bangkok 10330, Thailand
[4] Kasetsart Univ OmiKU, Omics Ctr Agr Bioresources Food & Hlth, Bangkok 10900, Thailand
[5] Kasetsart Univ, Fac Sci, Dept Zool, Bangkok 10900, Thailand
来源
MOLECULES | 2023年 / 28卷 / 01期
关键词
antiviral; peptide; hemp; SARS-CoV-2 main protease; molecular docking; ANTIMICROBIAL PEPTIDES; MOLECULAR-DYNAMICS; SIDE-CHAIN; WEB SERVER; IDENTIFICATION; ANTIOXIDANT; PREDICTION; DESIGN; SYSTEM; TOOL;
D O I
10.3390/molecules28010050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To control the COVID-19 pandemic, antivirals that specifically target the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently required. The 3-chymotrypsin-like protease (3CLpro) is a promising drug target since it functions as a catalytic dyad in hydrolyzing polyprotein during the viral life cycle. Bioactive peptides, especially food-derived peptides, have a variety of functional activities, including antiviral activity, and also have a potential therapeutic effect against COVID-19. In this study, the hemp seed trypsinized peptidome was subjected to computer-aided screening against the 3CLpro of SARS-CoV-2. Using predictive trypsinized products of the five major proteins in hemp seed (i.e., edestin 1, edestin 2, edestin 3, albumin, and vicilin), the putative hydrolyzed peptidome was established and used as the input dataset. To select the Cannabis sativa antiviral peptides (csAVPs), a predictive bioinformatic analysis was performed by three webserver screening programs: iAMPpred, AVPpred, and Meta-iAVP. The amino acid composition profile comparison was performed by COPid to screen for the non-toxic and non-allergenic candidates, ToxinPred and AllerTOP and AllergenFP, respectively. GalaxyPepDock and HPEPDOCK were employed to perform the molecular docking of all selected csAVPs to the 3CLpro of SARS-CoV-2. Only the top docking-scored candidate (csAVP4) was further analyzed by molecular dynamics simulation for 150 nanoseconds. Molecular docking and molecular dynamics revealed the potential ability and stability of csAVP4 to inhibit the 3CLpro catalytic domain with hydrogen bond formation in domain 2 with short bonding distances. In addition, these top ten candidate bioactive peptides contained hydrophilic amino acid residues and exhibited a positive net charge. We hope that our results may guide the future development of alternative therapeutics against COVID-19.
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页数:20
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