Department of Medical Biotechnology, University of Siena, 53100 Siena, Italy.
Department of Life Sciences, University of Siena, 53100 Siena, Italy.
J Med Chem. 2024 Sep 26;67(18):16145-16156. doi: 10.1021/acs.jmedchem.4c00810. Epub 2024 Sep 11.
Antibiotic resistance is a major global health threat, necessitating the development of new treatments and diverse molecules to combat severe infections and preserve the efficacy of existing drugs. Antimicrobial peptides (AMPs) offer a versatile arsenal against bacteria, and peptide structure branching can enhance their resistance to proteases and improve their overall efficacy. A small library of peptides derived from natural host defense peptides and synthesized in a tetrabranched form was selected against . Six selected branched peptides were further studied for antibacterial activity against a panel of strains, biofilm inhibition, protease resistance, and cytotoxicity. Their structure was predicted computationally and their mechanism of action was investigated by electron microscopy and by using fluorescent dyes. The peptide BAMP2 showed promise in a mouse skin infection model, indicating the potential for local infection treatment.
抗生素耐药性是一个全球性的主要健康威胁,需要开发新的治疗方法和多样化的分子来对抗严重感染并保持现有药物的疗效。抗菌肽 (AMPs) 为对抗细菌提供了多样化的武器,而肽结构分支可以增强它们对蛋白酶的抗性并提高它们的整体疗效。从天然宿主防御肽中衍生出的一小部分肽,并以四分支形式合成,被选中用于对抗 。针对一组菌株、生物膜抑制、蛋白酶抗性和细胞毒性进一步研究了 6 种选定的分支肽的抗菌活性。通过计算预测了它们的结构,并通过电子显微镜和荧光染料研究了它们的作用机制。肽 BAMP2 在小鼠皮肤感染模型中表现出良好的效果,表明其具有局部感染治疗的潜力。