抗菌剂
抗菌肽
抗生素
药品
广谱
生化工程
生物技术
计算生物学
生物
化学
药理学
组合化学
微生物学
工程类
作者
Alicia Boto,José Manuel Pérez de la Lastra,Concepción C. González
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2018-02-01
卷期号:23 (2): 311-311
被引量:120
标识
DOI:10.3390/molecules23020311
摘要
Host-defense peptides, also called antimicrobial peptides (AMPs), whose protective action has been used by animals for millions of years, fulfill many requirements of the pharmaceutical industry, such as: (1) broad spectrum of activity; (2) unlike classic antibiotics, they induce very little resistance; (3) they act synergically with conventional antibiotics; (4) they neutralize endotoxins and are active in animal models. However, it is considered that many natural peptides are not suitable for drug development due to stability and biodisponibility problems, or high production costs. This review describes the efforts to overcome these problems and develop new antimicrobial drugs from these peptides or inspired by them. The discovery process of natural AMPs is discussed, as well as the development of synthetic analogs with improved pharmacological properties. The production of these compounds at acceptable costs, using different chemical and biotechnological methods, is also commented. Once these challenges are overcome, a new generation of versatile, potent and long-lasting antimicrobial drugs is expected.
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