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抗菌肽免疫生物学进展

Advances in antimicrobial peptide immunobiology.

作者信息

Yount Nannette Y, Bayer Arnold S, Xiong Yan Q, Yeaman Michael R

机构信息

Division of Infectious Diseases, Harbor-UCLA Medical Center, Torrance, CA 90509, USA.

出版信息

Biopolymers. 2006;84(5):435-58. doi: 10.1002/bip.20543.

Abstract

Antimicrobial peptides are ancient components of the innate immune system and have been isolated from organisms spanning the phylogenetic spectrum. Over an evolutionary time span, these peptides have retained potency, in the face of highly mutable target microorganisms. This fact suggests important coevolutionary influences in the host-pathogen relationship. Despite their diverse origins, the majority of antimicrobial peptides have common biophysical parameters that are likely essential for activity, including small size, cationicity, and amphipathicity. Although more than 900 different antimicrobial peptides have been characterized, most can be grouped as belonging to one of three structural classes: (1) linear, often of alpha-helical propensity; (2) cysteine stabilized, most commonly conforming to beta-sheet structure; and (3) those with one or more predominant amino acid residues, but variable in structure. Interestingly, these biophysical and structural features are retained in ribosomally as well as nonribosomally synthesized peptides. Therefore, it appears that a relatively limited set of physicochemical features is required for antimicrobial peptide efficacy against a broad spectrum of microbial pathogens. During the past several years, a number of themes have emerged within the field of antimicrobial peptide immunobiology. One developing area expands upon known microbicidal mechanisms of antimicrobial peptides to include targets beyond the plasma membrane. Examples include antimicrobial peptide activity involving structures such as extracellular polysaccharide and cell wall components, as well as the identification of an increasing number of intracellular targets. Additional areas of interest include an expanding recognition of antimicrobial peptide multifunctionality, and the identification of large antimicrobial proteins, and antimicrobial peptide or protein fragments derived thereof. The following discussion highlights such recent developments in antimicrobial peptide immunobiology, with an emphasis on the biophysical aspects of host-defense polypeptide action and mechanisms of microbial resistance.

摘要

抗菌肽是先天性免疫系统的古老组成部分,已从跨越系统发育谱的生物体中分离出来。在进化的时间跨度内,面对高度易变的目标微生物,这些肽仍保持效力。这一事实表明宿主 - 病原体关系中存在重要的共同进化影响。尽管抗菌肽起源多样,但大多数具有共同的生物物理参数,这些参数可能对活性至关重要,包括小尺寸、阳离子性和两亲性。虽然已鉴定出900多种不同的抗菌肽,但大多数可归为以下三种结构类别之一:(1)线性的,通常具有α - 螺旋倾向;(2)由半胱氨酸稳定的,最常见的是符合β - 折叠结构;(3)具有一个或多个主要氨基酸残基但结构可变的。有趣的是,这些生物物理和结构特征在核糖体合成以及非核糖体合成的肽中都得以保留。因此,抗菌肽对广谱微生物病原体发挥功效似乎需要相对有限的一组物理化学特征。在过去几年中,抗菌肽免疫生物学领域出现了一些主题。一个发展领域扩展了已知的抗菌肽杀菌机制,以包括质膜之外的靶点。例子包括涉及细胞外多糖和细胞壁成分等结构的抗菌肽活性,以及越来越多细胞内靶点的鉴定。其他感兴趣的领域包括对抗菌肽多功能性的认识不断扩大,以及大型抗菌蛋白和由此衍生的抗菌肽或蛋白片段的鉴定。以下讨论重点介绍抗菌肽免疫生物学的这些最新进展,重点是宿主防御多肽作用的生物物理方面以及微生物抗性机制。

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