抗菌肽及其组装

Ana Maria Carmona-Ribeiro
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引用次数: 0

摘要

抗生素耐药性需要替代方案来对抗多重耐药菌株。抗菌肽(AMPs)的作用是破坏或溶解微生物细胞壁或细胞膜,其机制很难从微生物的角度进行抵消。本文讨论了抗菌肽及其组装体的结构-活性关系,不仅考虑了它们的自组装,还考虑了它们与载体的相互作用以获得最佳递送,或者它们与其他互补抗菌素或与其化学结构共价结合的部分的组合。还评估了配方对AMP活性的影响,揭示了无数的可能性。根据AMP、载体或添加到配方中的元素之间的相互作用力,AMP的活性可以降低、增强或保持不受影响。保护amp免受蛋白水解的方法也可能降低其活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobial Peptides and Their Assemblies
Antibiotic resistance requires alternatives to fight multi-drug resistant strains. Antimicrobial peptides (AMPs) act by disrupting or solubilizing microbial cell walls or membranes in accordance with mechanisms difficult to counteract from the microbe’s point of view. In this review, structure–activity relationships for AMPs and their assemblies are discussed, considering not only their self-assembly but also their interactions with their carriers for optimal delivery or their combinations with other complementary antimicrobials or moieties covalently bound to their chemical structure. The effect of the formulations on AMP activity is also evaluated, revealing a myriad of possibilities. Depending on the interaction forces between the AMP, the carrier, or the elements added to the formulations, AMP activity can be reduced, enhanced, or remain unaffected. Approaches protecting AMPs against proteolysis may also reduce their activity.
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