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本文引用的文献

1
Human Cathelicidin Inhibits SARS-CoV-2 Infection: Killing Two Birds with One Stone.人源防御素抑制 SARS-CoV-2 感染:一石二鸟。
ACS Infect Dis. 2021 Jun 11;7(6):1545-1554. doi: 10.1021/acsinfecdis.1c00096. Epub 2021 Apr 14.
2
Cathelicidin antimicrobial peptides suppress EV71 infection via regulating antiviral response and inhibiting viral binding.抗菌肽 cathelicidin 通过调节抗病毒反应和抑制病毒结合来抑制 EV71 感染。
Antiviral Res. 2021 Mar;187:105021. doi: 10.1016/j.antiviral.2021.105021. Epub 2021 Jan 26.
3
Application of and HTS Approaches to Identify Nuclear Import Inhibitors for Venezuelan Equine Encephalitis Virus Capsid Protein: A Case Study.应用高通量筛选方法鉴定委内瑞拉马脑炎病毒衣壳蛋白的核输入抑制剂:一个案例研究。
Front Chem. 2020 Dec 23;8:573121. doi: 10.3389/fchem.2020.573121. eCollection 2020.
4
A high-throughput drug screening strategy against coronaviruses.一种高通量抗冠状病毒药物筛选策略。
Int J Infect Dis. 2021 Feb;103:300-304. doi: 10.1016/j.ijid.2020.12.033. Epub 2020 Dec 14.
5
DBAASP v3: database of antimicrobial/cytotoxic activity and structure of peptides as a resource for development of new therapeutics.DBAASP v3:抗菌/细胞毒性肽的活性和结构数据库,是开发新疗法的资源。
Nucleic Acids Res. 2021 Jan 8;49(D1):D288-D297. doi: 10.1093/nar/gkaa991.
6
Machine learning-guided discovery and design of non-hemolytic peptides.机器学习指导的非溶血肽的发现和设计。
Sci Rep. 2020 Oct 6;10(1):16581. doi: 10.1038/s41598-020-73644-6.
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Alchemical Binding Free Energy Calculations in AMBER20: Advances and Best Practices for Drug Discovery.在 AMBER20 中进行的炼金术结合自由能计算:药物发现的进展和最佳实践。
J Chem Inf Model. 2020 Nov 23;60(11):5595-5623. doi: 10.1021/acs.jcim.0c00613. Epub 2020 Sep 16.
8
Broad-Spectrum Antiviral Entry Inhibition by Interfacially Active Peptides.界面活性肽的广谱抗病毒进入抑制作用。
J Virol. 2020 Nov 9;94(23). doi: 10.1128/JVI.01682-20.
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Bioinformatic Analysis of 1000 Amphibian Antimicrobial Peptides Uncovers Multiple Length-Dependent Correlations for Peptide Design and Prediction.对1000种两栖类抗菌肽的生物信息学分析揭示了肽设计与预测中多种长度依赖性相关性。
Antibiotics (Basel). 2020 Aug 7;9(8):491. doi: 10.3390/antibiotics9080491.
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Antiviral and Immunomodulatory Properties of Antimicrobial Peptides Produced by Human Keratinocytes.人角质形成细胞产生的抗菌肽的抗病毒和免疫调节特性
Front Microbiol. 2020 Jun 3;11:1155. doi: 10.3389/fmicb.2020.01155. eCollection 2020.

天然抗菌肽可作为新型抗病毒药物的来源。

Natural antimicrobial peptides as a source of new antiviral agents.

机构信息

Laboratory of Antiviral Drug Discovery, Institute of Molecular Biology of NAS, 0014, Yerevan, Armenia.

Denovo Sciences CJSC, 0033, Yerevan, Armenia.

出版信息

J Gen Virol. 2021 Sep;102(9). doi: 10.1099/jgv.0.001661.

DOI:10.1099/jgv.0.001661
PMID:34554085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10026734/
Abstract

Current antiviral drugs are limited because of their adverse side effects and increased rate of resistance. In recent decades, much scientific effort has been invested in the discovery of new synthetic and natural compounds with promising antiviral properties. Among this new generation of compounds, antimicrobial peptides with antiviral activity have been described and are attracting attention due to their mechanism of action and biological properties. To understand the potential of antiviral peptides (AVPs), we analyse the antiviral activity of well-known AVP families isolated from different natural sources, discuss their physical-chemical properties, and demonstrate how AVP databases can guide us to design synthetic AVPs with better therapeutic properties. All considerations in this sphere of antiviral therapy clearly demonstrate the remarkable contribution that AVPs may make in conquering old as well as newly emerging viruses that plague humanity.

摘要

由于其不良反应和耐药率增加,目前的抗病毒药物受到限制。近几十年来,科学家们投入了大量精力来发现具有有前景的抗病毒特性的新合成和天然化合物。在这新一代化合物中,具有抗病毒活性的抗菌肽已经被描述出来,并因其作用机制和生物学特性而引起关注。为了了解抗病毒肽 (AVP) 的潜力,我们分析了从不同天然来源分离得到的知名 AVP 家族的抗病毒活性,讨论了它们的理化性质,并展示了 AVP 数据库如何指导我们设计具有更好治疗特性的合成 AVP。在抗病毒治疗领域的所有考虑因素都清楚地表明,AVP 可能在攻克困扰人类的旧有和新出现的病毒方面做出显著贡献。