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Membrane-Interacting Antifungal Peptides

机译:膜相互作用的抗真菌肽

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The incidence of invasive fungal infections is increasing worldwide, resulting in more than 1.6 million deaths every year. Due to growing antifungal drug resistance and the limited number of currently used antimycotics, there is a clear need for novel antifungal strategies. In this context, great potential is attributed to antimicrobial peptides (AMPs) that are part of the innate immune system of organisms. These peptides are known for their broad-spectrum activity that can be directed toward bacteria, fungi, viruses and/or even cancer cells. Some AMPs act via rapid physical disruption of microbial cell membranes at high concentrations causing cell leakage and cell death. However, more complex mechanisms are also observed, such as interaction with specific lipids, production of reactive oxygen species, programmed cell death and autophagy. This review summarizes the structure and mode of action of antifungal AMPs, thereby focusing on their interaction with fungal membranes.
机译:侵袭性真菌感染的发病率在全世界增加,导致每年超过160万人死亡。 由于抗真菌药物耐药增长和目前使用的抗菌学的有限数量,有明确需要新的抗真菌策略。 在这种情况下,巨大的潜力归因于作为生物体的先天免疫系统的一部分的抗微生物肽(AMP)。 这些肽是众所周知的广谱活性,其可以针对细菌,真菌,病毒和/或甚至癌细胞。 一些AMPS通过在高浓度下的微生物细胞膜的快速体力破坏引起细胞泄漏和细胞死亡。 然而,也观察到更复杂的机制,例如与特异性脂质的相互作用,反应性氧的产生,具有编程的细胞死亡和自噬。 本综述总结了抗真菌AMPS的结构和作用方式,从而专注于它们与真菌膜的相互作用。

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