The Exploration of Bioactive Peptides that Docked to SARS-CoV-2 Spike Protein from Goats’ Milk Beta-Casein by In Silico

Q3 Chemistry Molekul Pub Date : 2023-11-20 DOI:10.20884/1.jm.2023.18.3.7297
H. S. Widodo, T. W. Murti, Ali Agus, A. Pertiwiningrum
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Abstract

Beta-casein in milk is known to be a bioactive peptide producer because of its amino acid sequence. Bioactive peptides have prospected molecules that can adhere with SARS-CoV-2 spike protein, so they can inhibit the virus from hooking up with human cell receptor protein. The research is aimed to find any peptides from goat’s milk beta-casein that are prospective candidates as SARS-CoV-2 spike protein inhibitors. Goat’s milk beta-casein was simulated as being digested by the digestive tract. Pepsin, trypsin, and chymotrypsin enzymes cut the beta-casein amino acids sequence into small peptides. Then, their bioavailability was predicted by Lipinski’s Rules of 5 (Ro5), any most fitted peptides to the rules will be simulated to dock to SARS-CoV2 spike protein besides Curcumin as the control ligand. Peptides with the best bind activity with the spike protein will be selected as inhibitor candidates. Peptide QPK is selected as a SARS-CoV-2 inhibitor candidate because it has better affinity energy than Curcumin or other selected peptides.
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通过硅学方法探索与山羊奶β-酪蛋白中的 SARS-CoV-2 Spike 蛋白对接的生物活性肽
牛奶中的β-酪蛋白因其氨基酸序列而被称为生物活性肽。生物活性肽有望成为能与 SARS-CoV-2 棘突蛋白结合的分子,从而抑制病毒与人体细胞受体蛋白结合。这项研究的目的是从山羊奶 beta-酪蛋白中寻找有望成为 SARS-CoV-2 尖峰蛋白抑制剂的多肽。山羊奶 beta-酪蛋白被模拟为可被消化道消化。胃蛋白酶、胰蛋白酶和糜蛋白酶将β-酪蛋白氨基酸序列切割成小肽。除了姜黄素作为对照配体外,任何最符合规则的多肽都将被模拟与 SARS-CoV2 尖峰蛋白对接。与尖峰蛋白结合活性最佳的多肽将被选为候选抑制剂。多肽 QPK 被选为 SARS-CoV-2 候选抑制剂,因为它比姜黄素或其他选定的多肽具有更好的亲和能。
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来源期刊
Molekul
Molekul Chemistry-Chemistry (all)
CiteScore
1.30
自引率
0.00%
发文量
31
审稿时长
4 weeks
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