Identification of nut protein-derived peptides against SARS-CoV-2 spike protein and main protease

被引:10
|
作者
Zhao, Wenzhu [1 ]
Xu, Ge [1 ]
Yu, Zhipeng [1 ]
Li, Jianrong [1 ]
Liu, Jingbo [2 ]
机构
[1] Bohai Univ, Coll Food Sci & Engn, Jinzhou 121013, Peoples R China
[2] Jilin Univ, Lab Nutr & Funct Food, Changchun 130062, Peoples R China
关键词
Molecular docking; Molecular dynamics simulation; Nut proteins; SARS-COV-2; Mpro; SARS-CoV-2 spike RBD; INHIBITORS;
D O I
10.1016/j.compbiomed.2021.104937
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recently, an outbreak of a novel coronavirus disease (COVID-19) has reached pandemic proportions, and there is an urgent need to develop nutritional supplements to assist with prevention, treatment, and recovery. In this study, SARS-CoV-2 inhibitory peptides were screened from nut proteins in silico, and binding affinities of the peptides to the SARS-CoV-2 main protease (Mpro) and the spike protein receptor-binding domain (RBD) were evaluated. Peptide NDQF from peanuts and peptide ASGCGDC from almonds were found to have a strong binding affinity for both targets of the coronavirus. The binding sites of the NDQF and ASGCGDC peptides are highly consistent with the Mpro inhibitor N3. In addition, NDQF and ASGCGDC exhibited an effective binding affinity for amino acid residues Tyr453 and Gln493 of the spike RBD. Molecular dynamics simulation further confirmed that the NDQF and ASGCGDC peptides could bind stably to the SARS-COV-2 Mpro and spike RBD. In summary, nut protein may be helpful as nutritional supplements for COVID-19 patients, and the screened peptides could be considered a potential lead compound for designing entry inhibitors against SARS-CoV-2.
引用
收藏
页数:8
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