Kim Dong Yun, Oh You Bin, Park Je Seon, Min Yu-Hong, Park Min Chul
College of Pharmacy, Inje Institute of Pharmaceutical Sciences and Research, Inje University, Gimhae 50832, Republic of Korea.
Department of Pharmaceutical Engineering, Inje University, Gimhae 50832, Republic of Korea.
Antibiotics (Basel). 2024 Mar 5;13(3):239. doi: 10.3390/antibiotics13030239.
Many anti-microbial peptides (AMPs) and pro-apoptotic peptides are considered as novel anti-microbial agents, distinguished by their different characteristics. Nevertheless, AMPs exhibit certain limitations, including poor stability and potential toxicity, which hinder their suitability for applications in pharmaceutics and medical devices. In this study, we used recombinant mussel adhesive protein (MAP) as a robust scaffold to overcome these limitations associated with AMPs. Mussel adhesive protein fused with functional peptides (MAP-FPs) was used to evaluate anti-microbial activities, minimal inhibitory concentration (MIC), and time-kill kinetics (TKK) assays against six of bacteria strains. MAP and MAP-FPs were proved to have an anti-microbial effect with MIC of 4 or 8 µM against only Gram-negative bacteria strains. All tested MAP-FPs killed four different Gram-negative bacteria strains within 180 min. Especially, MAP-FP-2 and -5 killed three Gram-negative bacteria strain, including , , and , within 10 min. A cytotoxicity study using Vero and HEK293T cells indicated the safety of MAP and MAP-FP-2 and -3. Thermal stability of MAP-FP-2 was also validated by HPLC analysis at an accelerated condition for 4 weeks. This study identified that MAP-FPs have novel anti-microbial activity, inhibiting the growth and rapidly killing Gram-negative bacteria strains with high thermal stability and safety.
许多抗菌肽(AMPs)和促凋亡肽被认为是新型抗菌剂,它们具有不同的特性。然而,抗菌肽存在一定的局限性,包括稳定性差和潜在毒性,这阻碍了它们在制药和医疗器械中的应用。在本研究中,我们使用重组贻贝粘附蛋白(MAP)作为一种强大的支架来克服与抗菌肽相关的这些局限性。将贻贝粘附蛋白与功能肽融合(MAP-FPs)用于评估对六种细菌菌株的抗菌活性、最低抑菌浓度(MIC)和时间杀灭动力学(TKK)测定。MAP和MAP-FPs被证明仅对革兰氏阴性菌菌株具有抗菌作用,MIC为4或8μM。所有测试的MAP-FPs在180分钟内杀死了四种不同的革兰氏阴性菌菌株。特别是,MAP-FP-2和-5在10分钟内杀死了三种革兰氏阴性菌菌株,包括 、 和 。使用Vero和HEK293T细胞进行的细胞毒性研究表明MAP以及MAP-FP-2和-3是安全的。通过在加速条件下进行4周的高效液相色谱分析,也验证了MAP-FP-2的热稳定性。本研究确定MAP-FPs具有新型抗菌活性,能够抑制革兰氏阴性菌菌株的生长并快速杀死它们,且具有高热稳定性和安全性。