Shao Changxuan, Wang Mengcheng, Wang Yuanmengxue, He Shiqi, Zhu Yongjie, Shan Anshan
College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, Heilongjiang, China.
Sheng Wu Gong Cheng Xue Bao. 2024 Dec 25;40(12):4396-4407. doi: 10.13345/j.cjb.240077.
Antimicrobial peptides (AMPs) are small molecular peptides widely existing in the innate immunity of organisms, serving as the first line of defense. Natural AMPs possess various biological activities and are difficult to develop drug resistance. However, they are easily broken down by digestive enzymes in the body. In recent years, increasing methods have been reported to enhance the stability of AMPs, including incorporation of unnatural amino acids, chemical modifications, strategic avoidance of enzyme cleavage sites, cyclization, and nano peptide design. This review summarizes the methods for improving the stability of AMPs against protease degradation, aiming to provide references for further research in this field.
抗菌肽(AMPs)是广泛存在于生物体固有免疫中的小分子肽,作为第一道防线。天然抗菌肽具有多种生物活性,且难以产生耐药性。然而,它们很容易被体内的消化酶分解。近年来,已有越来越多的方法被报道用于提高抗菌肽的稳定性,包括引入非天然氨基酸、化学修饰、策略性避开酶切位点、环化以及纳米肽设计。本综述总结了提高抗菌肽抗蛋白酶降解稳定性的方法,旨在为该领域的进一步研究提供参考。