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用于治疗应用的工程抗真菌肽的策略和机会。

Strategies and opportunities for engineering antifungal peptides for therapeutic applications.

机构信息

Department of Chemical and Biomolecular Engineering, University of Maryland, 2113 Chemical and Nuclear Engineering Building (#090), 4418 Stadium Drive, College Park, MD 20742, USA.

Department of Chemical and Biomolecular Engineering, University of Maryland, 2113 Chemical and Nuclear Engineering Building (#090), 4418 Stadium Drive, College Park, MD 20742, USA.

出版信息

Curr Opin Biotechnol. 2023 Jun;81:102926. doi: 10.1016/j.copbio.2023.102926. Epub 2023 Apr 5.

DOI:10.1016/j.copbio.2023.102926
PMID:37028003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10229436/
Abstract

Antifungal peptides (AFPs) are widely described as promising prospects to treat and prevent fungal infections, though they are far less studied than their antibacterial counterparts. Although promising, AFPs have practical limitations that have hindered their use as therapeutics. Rational design and combinatorial engineering are powerful protein engineering strategies with much potential to address the limitations of AFPs by designing peptides with improved physiochemical and biological characteristics. We examine how rational design and combinatorial engineering approaches have already been used to improve the properties of AFPs and propose key opportunities for applying these strategies to push the design and application of AFPs forward.

摘要

抗菌肽(AFPs)被广泛描述为治疗和预防真菌感染的有前途的方法,尽管它们的研究远不及抗菌肽广泛。尽管有前景,但 AFPs 存在实际限制,这阻碍了它们作为治疗剂的应用。理性设计和组合工程是强大的蛋白质工程策略,具有很大的潜力通过设计具有改进的物理化学和生物学特性的肽来解决 AFPs 的局限性。我们研究了理性设计和组合工程方法如何已经被用于改善 AFPs 的性质,并提出了应用这些策略的关键机会,以推动 AFPs 的设计和应用。

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Antimicrobial Peptide Mechanism Studied by Scattering-Guided Molecular Dynamics Simulation.基于散射引导分子动力学模拟研究抗菌肽的作用机制。
J Phys Chem B. 2022 Sep 15;126(36):6922-6935. doi: 10.1021/acs.jpcb.2c03193. Epub 2022 Sep 6.
2
Editorial: Antifungal Pipeline: Build It Strong; Build It Better!社论:抗真菌药物研发渠道:筑牢根基;精益求精!
Front Cell Infect Microbiol. 2022 Mar 16;12:881272. doi: 10.3389/fcimb.2022.881272. eCollection 2022.
3
Accelerating the discovery of antifungal peptides using deep temporal convolutional networks.
在分泌型天冬氨酸蛋白酶和唾液蛋白酶存在的情况下,氨基酸取代对组蛋白5蛋白水解稳定性的作用。
Protein Sci. 2025 Jan;34(1):e70011. doi: 10.1002/pro.70011.
4
Biomimetic Antifungal Materials: Countering the Challenge of Multidrug-Resistant Fungi.仿生抗真菌材料:应对多重耐药真菌的挑战
Biomimetics (Basel). 2024 Jul 12;9(7):425. doi: 10.3390/biomimetics9070425.
5
Exploring the frontiers of therapeutic breadth of antifungal peptides: A new avenue in antifungal drugs.探索抗真菌肽治疗广度的前沿:抗真菌药物的新途径。
J Ind Microbiol Biotechnol. 2024 Jan 9;51. doi: 10.1093/jimb/kuae018.
6
Various Biomimetics, Including Peptides as Antifungals.各种仿生学,包括用作抗真菌剂的肽。
Biomimetics (Basel). 2023 Oct 28;8(7):513. doi: 10.3390/biomimetics8070513.
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Candida albicans and Antifungal Peptides.白色念珠菌与抗真菌肽
Infect Dis Ther. 2023 Dec;12(12):2631-2648. doi: 10.1007/s40121-023-00889-9. Epub 2023 Nov 8.
使用深度时间卷积网络加速抗真菌肽的发现。
Brief Bioinform. 2022 Mar 10;23(2). doi: 10.1093/bib/bbac008.
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Phage display-based discovery of cyclic peptides against the broad spectrum bacterial anti-virulence target CsrA.基于噬菌体展示的广谱细菌抗毒力靶标 CsrA 环肽发现。
Eur J Med Chem. 2022 Mar 5;231:114148. doi: 10.1016/j.ejmech.2022.114148. Epub 2022 Jan 24.
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Annu Rev Immunol. 2022 Apr 26;40:121-141. doi: 10.1146/annurev-immunol-101220-034306. Epub 2022 Jan 10.
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Evolution-Based Protein Engineering for Antifungal Peptide Improvement.基于进化的抗菌肽改造的蛋白质工程。
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The Consequences of Our Changing Environment on Life Threatening and Debilitating Fungal Diseases in Humans.我们不断变化的环境对人类危及生命和使人衰弱的真菌疾病的影响。
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