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内溶素和膜活性肽:针对革兰氏阴性菌的创新工程策略。

Endolysins and membrane-active peptides: innovative engineering strategies against gram-negative bacteria.

作者信息

Wojciechowska Monika

机构信息

University of Warsaw, Centre of New Technologies, Warsaw, Poland.

出版信息

Front Microbiol. 2025 Jun 3;16:1603380. doi: 10.3389/fmicb.2025.1603380. eCollection 2025.

Abstract

Endolysins, bacteriophage-encoded peptidoglycan hydrolases, offer promising potential in antibacterial therapy, including treatments targeting gram-negative bacteria. While these enzymes naturally act primarily on gram-positive bacteria, their application against gram-negative pathogens is more challenging due to the presence of a dual-layer cell membrane, which acts as a protective barrier. However, innovative approaches, such as fusing endolysins with antimicrobial peptides (AMPs), have demonstrated increased efficacy against gram-negative bacteria. Modifying endolysins by introducing hydrophobic properties or positive charges or combining them with agents that disrupt the outer membrane enhances their bactericidal activity. Moreover, phage endolysins that exhibit activity against gram-negative bacteria are a promising source of membrane-active peptides. Identifying new peptide sequences derived from endolysins capable of penetrating the bacterial cell membrane represents a novel and increasingly explored research direction. Studying these innovative strategies had yielded promising results, though the field remains under active investigation and development. Ongoing efforts aim to optimize these approaches to improve their effectiveness against antibiotic-resistant gram-negative bacterial strains, which are particularly difficult to treat with conventional antibiotics. This review summarizes the latest advancements and solutions in the field, highlighting the potential of endolysins and membrane-active peptides as next-generation antibacterial agents.

摘要

内溶素是噬菌体编码的肽聚糖水解酶,在抗菌治疗中具有广阔的应用前景,包括针对革兰氏阴性菌的治疗。虽然这些酶天然主要作用于革兰氏阳性菌,但由于存在双层细胞膜这一保护屏障,它们对革兰氏阴性病原体的应用更具挑战性。然而,创新方法,如将内溶素与抗菌肽(AMPs)融合,已证明对革兰氏阴性菌的疗效有所提高。通过引入疏水性或正电荷来修饰内溶素,或将它们与破坏外膜的试剂结合,可增强其杀菌活性。此外,对革兰氏阴性菌具有活性的噬菌体内溶素是有前景的膜活性肽来源。鉴定源自能够穿透细菌细胞膜的内溶素的新肽序列是一个新颖且探索日益深入的研究方向。研究这些创新策略已取得了有前景的结果,不过该领域仍在积极研究和开发中。正在进行的努力旨在优化这些方法,以提高它们对抗生素耐药革兰氏阴性菌菌株的有效性,这些菌株用传统抗生素特别难以治疗。本综述总结了该领域的最新进展和解决方案,突出了内溶素和膜活性肽作为下一代抗菌剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfa/12170589/e12dc4c4b6b7/fmicb-16-1603380-g001.jpg

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