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Antimicrobial Peptides: Interaction With Model and Biological Membranes and Synergism With Chemical Antibiotics

机译:抗菌肽:与模型和生物膜的相互作用以及与化学抗生素的协同作用

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Abstract Antimicrobial peptides (AMPs) are promising novel antibiotics since they have shown antimicrobial activity against a wide range of bacterial species, including multiresistant bacteria; however, toxicity is the major barrier to convert antimicrobial peptides into active drugs. A profound and proper understanding of the complex interactions between these peptides and biological membranes using biophysical tools and model membranes seems to be a key factor in the race to develop a suitable antimicrobial peptide therapy for clinical use. In the search for such therapy, different combined approaches with conventional antibiotics have been evaluated in recent years and demonstrated to improve the therapeutic potential of AMPs. Some of these approaches have revealed promising additive or synergistic activity between AMPs and chemical antibiotics. This review will give an insight into the possibilities that physicochemical tools can give in the AMPs research and also address the state of the art on the current promising combined therapies between AMPs and conventional antibiotics, which appear to be a plausible future opportunity for AMPs treatment.
机译:摘要抗菌肽(AMPs)是具有前景的新型抗生素,因为它们对多种细菌(包括多重耐药细菌)均显示出抗菌活性。然而,毒性是将抗菌肽转化为活性药物的主要障碍。使用生物物理工具和模型膜对这些肽与生物膜之间复杂相互作用的深刻而正确的理解,似乎是开发适合临床使用的抗菌肽治疗的关键因素。在寻找这种疗法时,近年来已对与常规抗生素的不同组合方法进行了评估,并证明可提高AMPs的治疗潜力。这些方法中的一些已经揭示了有希望的AMP与化学抗生素之间的加性或协同活性。这篇综述将深入探究理化工具在AMPs研究中可能带来的可能性,并探讨AMPs和常规抗生素之间当前有希望的联合疗法的最新技术水平,这似乎是AMPs治疗的未来可能机会。

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