肽
生物信息学
虚拟筛选
突变
化学
小分子
对接(动物)
生物化学
计算生物学
合理设计
定点突变
突变体
生物
药物发现
医学
遗传学
基因
护理部
作者
Aishwarya Kochhar,Noor Saba Khan,Ravi Deval,Dibyabhaba Pradhan,Lingaraja Jena,Rajabrata Bhuyan,Tanmaya Kumar Sahu,Arun K. Jain
出处
期刊:3 biotech
[Springer Nature]
日期:2021-05-31
卷期号:11 (6)
标识
DOI:10.1007/s13205-021-02856-y
摘要
Protein-protein interactions of Interleukin-17 (IL17) play vital role in the autoimmune and inflammatory diseases, such as rheumatoid arthritis, multiple sclerosis, and psoriasis. Potent therapeutics for these diseases could be developed by blocking or modulating these interactions through biologics, peptide inhibitors and small molecule inhibitors. Unlike biologics, peptide inhibitors are cost effective and can be orally available. Peptide inhibitors do not require a binding groove as that of small molecules either. Therefore, crystal structure of IL17A in complex with a high affinity peptide inhibitor (HAP) (1-IHVTIPADLWDWIN-14) is investigated with an aim to find hot spots that could improve its potency. An in silico mutagenesis strategy was implemented using FoldX PSSM to scan for positions tolerant to amino acid substitution. Three positions T4, A7, and N14 showed improved stability when mutated with 'F/M/Y', 'P' and 'F/M/Y', respectively. A set of 31 mutant peptides are designed through combinations of these tolerant mutations using Build Model application of FoldX. Binding affinity and interactions of 31 peptides are assessed through protein-peptide docking and binding free energy calculations. Two peptides namely, P1 ("1-IHVTIPPDLWDWIY-14") and P2 ("1-IHVMIPPDLWDWIF-14") showed better binding affinity to IL17A dimerization site compared to HAP. Interactions of P1, P2 and HAP are also analyzed through 100 ns molecular dynamics simulations using GROMACS v5.0. The results revealed that the P2 peptide likely to offer better potency compared to HAP and P1. Therefore, the P2 peptide can be synthesized to develop oral therapies for autoimmune and inflammatory diseases with further experimental evaluations.The online version contains supplementary material available at 10.1007/s13205-021-02856-y.
科研通智能强力驱动
Strongly Powered by AbleSci AI