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抗菌肽在抗生素前-后时代作为抗感染药物?

Antimicrobial Peptides as Anti-Infective Agents in Pre-Post-Antibiotic Era?

机构信息

Department of Biology, Faculty of Science, University of Split, 21000 Split, Croatia.

Laboratory for Aquaculture, Institute of Oceanography and Fisheries, 21000 Split, Croatia.

出版信息

Int J Mol Sci. 2019 Nov 14;20(22):5713. doi: 10.3390/ijms20225713.

Abstract

Resistance to antibiotics is one of the main current threats to human health and every year multi-drug resistant bacteria are infecting millions of people worldwide, with many dying as a result. Ever since their discovery, some 40 years ago, the antimicrobial peptides (AMPs) of innate defense have been hailed as a potential alternative to conventional antibiotics due to their relatively low potential to elicit resistance. Despite continued effort by both academia and start-ups, currently there are still no antibiotics based on AMPs in use. In this study, we discuss what we know and what we do not know about these agents, and what we need to know to successfully translate discovery to application. Understanding the complex mechanics of action of these peptides is the main prerequisite for identifying and/or designing or redesigning novel molecules with potent biological activity. However, other aspects also need to be well elucidated, i.e., the (bio)synthetic processes, physiological and pathological contexts of their activity, and a quantitative understanding of how physico-chemical properties affect activity. Research groups worldwide are using biological, biophysical, and algorithmic techniques to develop models aimed at designing molecules with the necessary blend of antimicrobial potency and low toxicity. Shedding light on some open questions may contribute toward improving this process.

摘要

抗生素耐药性是当前人类健康的主要威胁之一。每年,全球都有数百万人感染耐多药细菌,其中许多人因此死亡。自 40 年前发现以来,由于其产生耐药性的潜力相对较低,天然防御抗菌肽 (AMPs) 一直被誉为传统抗生素的潜在替代品。尽管学术界和初创企业都在不断努力,但目前仍没有基于 AMP 的抗生素投入使用。在这项研究中,我们讨论了我们对这些药物的了解和不了解的地方,以及为了成功将发现转化为应用,我们需要了解的地方。了解这些肽的复杂作用机制是识别和/或设计或重新设计具有强大生物学活性的新型分子的主要前提。然而,还需要阐明其他方面,即(生物)合成过程、它们活性的生理和病理背景,以及定量了解物理化学性质如何影响活性。世界各地的研究小组正在使用生物学、生物物理学和算法技术来开发旨在设计具有必要抗菌效力和低毒性的分子的模型。阐明一些悬而未决的问题可能有助于改进这一过程。

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