Zhang Ruonan, Wu Di, Gao Yitian
School of Life and Environmental Sciences, Wenzhou University, Wenzhou, Zhejiang 325000, P. R. China.
School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325000, P. R. China.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2022 Dec 25;39(6):1247-1253. doi: 10.7507/1001-5515.202206017.
Antimicrobial peptides (AMPs) are a class of peptides widely existing in nature with broad-spectrum antimicrobial activity. It is considered as a new alternative to traditional antibiotics because of its unique mechanism of antimicrobial activity. The development and application of natural AMPs are limited due to their drawbacks such as low antimicrobial activity and unstable metabolism. Therefore, the design and optimization of derived peptides based on natural antimicrobial peptides have become recent research hotspots. In this paper, we focus on ribosomal AMPs and summarize the design and optimization strategies of some related derived peptides, which include reasonable primary structure modification, cyclization strategy and computer-aided strategy. We expect to provide ideas for the design and optimization of antimicrobial peptides and the development of anti-infective drugs through analysis and summary in this paper.
抗菌肽(AMPs)是一类广泛存在于自然界的具有广谱抗菌活性的肽。由于其独特的抗菌活性机制,它被认为是传统抗生素的一种新替代品。天然抗菌肽因其抗菌活性低、代谢不稳定等缺点,其开发和应用受到限制。因此,基于天然抗菌肽的衍生肽的设计与优化已成为近年来的研究热点。本文聚焦于核糖体抗菌肽,总结了一些相关衍生肽的设计与优化策略,包括合理的一级结构修饰、环化策略和计算机辅助策略。我们期望通过本文的分析和总结,为抗菌肽的设计与优化以及抗感染药物的开发提供思路。