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膜破坏肽作用机制的最新进展

Latest developments on the mechanism of action of membrane disrupting peptides.

作者信息

Pandidan Sara, Mechler Adam

机构信息

La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Australia.

出版信息

Biophys Rep. 2021 Jun 30;7(3):173-184. doi: 10.52601/bpr.2021.200037.

DOI:10.52601/bpr.2021.200037
PMID:37287489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10244799/
Abstract

Antimicrobial peptides (AMPs) are integral components of the innate immune defence system of all complex organisms including plants, insects, and mammals. They have wide range of antibacterial, antifungal, antiviral, and even anticancer activities, therefore AMPs are attractive candidates for developing novel therapeutic approaches. Cationic α-helical membrane disrupting peptides are perhaps the most widely studied subclass of AMPs due to their common fundamental characteristics that allow for detailed structure-function analysis and therefore offer a promising solution to the threat of multidrug resistant strains of bacteria. The majority of the studies of AMP activity focused on the biological and biophysical aspects of membrane disruption; the understanding of the molecular mechanism of action from the physicochemical point of view forms a relatively small subfield. This review will provide an overview of these works, focusing on the empirical and thermodynamic models of AMP action.

摘要

抗菌肽(AMPs)是包括植物、昆虫和哺乳动物在内的所有复杂生物体固有免疫防御系统的组成部分。它们具有广泛的抗菌、抗真菌、抗病毒甚至抗癌活性,因此抗菌肽是开发新型治疗方法的有吸引力的候选物。阳离子α-螺旋膜破坏肽可能是研究最广泛的抗菌肽亚类,因为它们具有共同的基本特征,便于进行详细的结构-功能分析,从而为多药耐药菌株的威胁提供了一个有前景的解决方案。大多数关于抗菌肽活性的研究集中在膜破坏的生物学和生物物理方面;从物理化学角度对抗菌肽作用分子机制的理解构成了一个相对较小的子领域。本综述将概述这些工作,重点关注抗菌肽作用的经验模型和热力学模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/dcbd77a124e2/br-7-3-173-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/2369439af075/br-7-3-173-1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/71d77df557a3/br-7-3-173-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/dcbd77a124e2/br-7-3-173-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/2369439af075/br-7-3-173-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/6dbda4db1110/br-7-3-173-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/71d77df557a3/br-7-3-173-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce41/10244799/dcbd77a124e2/br-7-3-173-4.jpg

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本文引用的文献

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Nano-viscosimetry analysis of the membrane disrupting action of the bee venom peptide melittin.纳米粘度法分析蜂毒肽 melittin 的膜破坏作用。
Sci Rep. 2019 Jul 25;9(1):10841. doi: 10.1038/s41598-019-47325-y.
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Mechanistic Landscape of Membrane-Permeabilizing Peptides.膜渗透肽的作用机制全景
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Antimicrobial Peptides: Diversity, Mechanism of Action and Strategies to Improve the Activity and Biocompatibility In Vivo.抗菌肽:多样性、作用机制和提高体内活性和生物相容性的策略。
抗菌肽:应对抗生素耐药性不断上升威胁的一种有前景的解决方案。
Pharmaceutics. 2024 Dec 2;16(12):1542. doi: 10.3390/pharmaceutics16121542.
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Antibiofilm Activity of Epinecidin-1 and Its Variants Against Drug-Resistant and Isolates from Vaginal Candidiasis Patients.抗菌肽-1及其变体对耐药性和阴道念珠菌病患者分离株的抗生物膜活性。
Infect Dis Rep. 2024 Dec 12;16(6):1214-1229. doi: 10.3390/idr16060096.
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Achieving Endo/Lysosomal Escape Using Smart Nanosystems for Efficient Cellular Delivery.利用智能纳米系统实现内体/溶酶体逃逸以实现有效的细胞递送。
Molecules. 2024 Jul 1;29(13):3131. doi: 10.3390/molecules29133131.
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4
Phenylalanine residues act as membrane anchors in the antimicrobial action of Aurein 1.2.苯丙氨酸残基在奥瑞因1.2的抗菌作用中充当膜锚定物。
Biointerphases. 2017 Oct 26;12(5):05G605. doi: 10.1116/1.4995674.
5
Membrane Core-Specific Antimicrobial Action of Cathelicidin LL-37 Peptide Switches Between Pore and Nanofibre Formation.抗菌肽 LL-37 通过在孔和纳米纤维形成之间切换发挥其针对细胞膜核心的抗菌作用。
Sci Rep. 2016 Nov 30;6:38184. doi: 10.1038/srep38184.
6
How Membrane-Active Peptides Get into Lipid Membranes.膜活性肽如何进入脂膜。
Acc Chem Res. 2016 Jun 21;49(6):1130-8. doi: 10.1021/acs.accounts.6b00074. Epub 2016 May 17.
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Optimal conditions for opening of membrane pore by amphiphilic peptides.两亲性肽打开膜孔的最佳条件。
J Chem Phys. 2015 Dec 28;143(24):243115. doi: 10.1063/1.4933229.
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Controls and constrains of the membrane disrupting action of Aurein 1.2.奥瑞因1.2膜破坏作用的控制与限制
Sci Rep. 2015 Nov 17;5:16378. doi: 10.1038/srep16378.
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Mammalian Antimicrobial Peptides: Promising Therapeutic Targets Against Infection and Chronic Inflammation.哺乳动物抗菌肽:对抗感染和慢性炎症的有前景的治疗靶点。
Curr Top Med Chem. 2016;16(1):99-129. doi: 10.2174/1568026615666150703121819.
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Potential of novel antimicrobial peptide P3 from bovine erythrocytes and its analogs to disrupt bacterial membranes in vitro and display activity against drug-resistant bacteria in a mouse model.牛红细胞新型抗菌肽P3及其类似物在体外破坏细菌膜并在小鼠模型中对耐药细菌显示活性的潜力。
Antimicrob Agents Chemother. 2015 May;59(5):2835-41. doi: 10.1128/AAC.04932-14. Epub 2015 Mar 9.