生物催化
背景(考古学)
化学
超分子化学
计算生物学
生化工程
计算机科学
二硫键
组合化学
动作(物理)
纳米技术
抗菌肽
行动地点
行动方式
蛋白质稳定性
班级(哲学)
氨基酸
肽
生物化学
作者
Samilla B. Rezende,Elizabete de Souza Cândido,Ludovico Migliolo,Marlon H. Cardoso,Octávio Luiz Franco
摘要
Antimicrobial resistance (AMR) is a global health problem, therefore, anti-AMR alternatives and strategies are required to develop effective therapeutics. Bearing this in mind, macrocyclic peptides (MCPs) that present cyclic scaffolds, disulfide bonds and constrained arrangements offer a distinct structural advantage that expands their potential mechanisms of action against pathogens. By modifying and improving this class of peptides, it is possible to obtain greater stability under extreme biological conditions and extended therapeutic windows, also enabling targeted action against intracellular pathogens. These advancements are driven by integrating computational tools, including artificial intelligence, to predict optimal sequences based on amino acid motifs, patterns, and physicochemical properties. Altogether, these approaches help us to design optimised MCPs and facilitate the development of more robust, selective and effective therapeutic agents tailored to combat AMR. In this review, we will explore recent advances in the context of AMR, integrating computational approaches for MCPs design, and proposed mechanisms of action for the next generation of MCP-based therapeutics.
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