Toke Orsolya
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Biopolymers. 2005;80(6):717-35. doi: 10.1002/bip.20286.
Antimicrobial peptides (AMPs) of innate origin are agents of the most ancient form of defense systems. They can be found in a wide variety of species ranging from bacteria through insects to humans. Through the course of evolution, host organisms developed arsenals of AMPs that protect them against a large variety of invading pathogens including both Gram-negative and Gram-positive bacteria. At a time of increasing bacterial resistance, AMPs have been the focus of investigation in a number of laboratories worldwide. Although recent studies show that some of the peptides are likely to have intracellular targets, the vast majority of AMPs appear to act by permeabilization of the bacterial cell membrane. Their activity and selectivity are governed by the physicochemical parameters of the peptide chains as well as the properties of the membrane system itself. In this review, we will summarize some of the recent developments that provide us with a better understanding of the mode of action of this unique family of antibacterial agents. Particular attention will be given to the determinants of AMP-lipid bilayer interactions as well as to the different pore formation mechanisms. The emphasis will be on linear AMPs but representatives of cysteine-bridged AMPs will also be discussed.
先天性抗菌肽(AMPs)是最古老的防御系统的组成部分。从细菌到昆虫再到人类,在各种各样的物种中都能找到它们。在进化过程中,宿主生物体形成了一系列抗菌肽,以保护它们免受包括革兰氏阴性菌和革兰氏阳性菌在内的多种入侵病原体的侵害。在细菌耐药性不断增加的时代,抗菌肽已成为全球众多实验室的研究重点。尽管最近的研究表明,其中一些肽可能具有细胞内靶点,但绝大多数抗菌肽似乎是通过使细菌细胞膜通透性增加而起作用的。它们的活性和选择性受肽链的物理化学参数以及膜系统本身特性的支配。在这篇综述中,我们将总结一些最新进展,这些进展使我们能更好地理解这一独特抗菌剂家族的作用模式。将特别关注抗菌肽与脂质双层相互作用以及不同孔形成机制的决定因素。重点将放在线性抗菌肽上,但也会讨论半胱氨酸桥连抗菌肽的代表。