Cândido Elizabete S, Cardoso Marlon H, Chan Lai Y, Torres Marcelo D T, Oshiro Karen G N, Porto William F, Ribeiro Suzana M, Haney Evan F, Hancock Robert E W, Lu Timothy K, de la Fuente-Nunez Cesar, Craik David J, Franco Octávio L
Centro de Análises Proteômicas e Bioquímicas, Pós-Graduação em Ciências Genômicas e Biotecnologia , Universidade Católica de Brasília , SGAN 916 Módulo B , Asa Norte, Brasília , Distrito Federal 70790160 , Brazil.
S-Inova Biotech, Programa de Pós-Graduação em Biotecnologia , Universidade Católica Dom Bosco , Avenida Tamandaré 6000 , Campo Grande , Mato Grosso do Sul 79117900 , Brazil.
ACS Infect Dis. 2019 Jul 12;5(7):1081-1086. doi: 10.1021/acsinfecdis.9b00073. Epub 2019 May 1.
Bacterial biofilms and associated infections represent one of the biggest challenges in the clinic, and as an alternative to counter bacterial infections, antimicrobial peptides have attracted great attention in the past decade. Here, ten short cationic antimicrobial peptides were generated through a sliding-window strategy on the basis of the 19-amino acid residue peptide, derived from a ribosomal protein. PaDBS1R6F10 exhibited anti-infective potential as it decreased the bacterial burden in murine cutaneous infections by more than 1000-fold. Adverse cytotoxic and hemolytic effects were not detected against mammalian cells. The peptide demonstrated structural plasticity in terms of its secondary structure in the different environments tested. PaDBS1R6F10 represents a promising antimicrobial agent against bacteria infections, without harming human cells.
细菌生物膜及相关感染是临床上最大的挑战之一,作为对抗细菌感染的一种替代方法,抗菌肽在过去十年中备受关注。在此,基于一种由核糖体蛋白衍生的19个氨基酸残基的肽,通过滑动窗口策略生成了十种短阳离子抗菌肽。PaDBS1R6F10表现出抗感染潜力,因为它使小鼠皮肤感染中的细菌载量降低了1000倍以上。未检测到对哺乳动物细胞的不良细胞毒性和溶血作用。该肽在不同测试环境中的二级结构方面表现出结构可塑性。PaDBS1R6F10是一种有前景的抗细菌感染抗菌剂,且不会伤害人类细胞。