Department of Molecular Microbiology and Biotechnology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Ilse Katz Institute for Nanotechnology, Ben Gurion University of the Negev, Beer Sheva, Israel.
mSphere. 2020 Apr 1;5(2):e00021-20. doi: 10.1128/mSphere.00021-20.
The rise of multidrug-resistant pathogens has awakened interest in new drug candidates such as antimicrobial peptides and their derivatives. Recent work suggests that some antimicrobial peptides have the ability to self-assemble into ordered amyloid-like nanostructures which facilitate their antibacterial activity. Here, we evaluate a histatin-based antimicrobial peptide, and its self-assembling derivative, in the interplay between self-assembly, membrane interactions, and antibacterial and antifungal activities. We demonstrate substantial membrane targeting by both peptides, as well as mechanistic insights into this mode of action, which correlates to their antifungal activity and is not affected by their self-assembling state. The ability to self-assemble does, however, significantly affect peptide antibacterial activity against both Gram-negative and Gram-positive bacteria. These results are surprising and hint at important distinctions between antifungal and antibacterial peptide activities in prokaryotes and eukaryotic microbes. Antimicrobial peptides are important modulators of host defense against bacterial, fungal, and viral pathogens in humans and other multicellular organisms. Two converging paradigms point to a link between antimicrobial peptides that self-assemble into amyloid-like nanoassemblies and classical amyloidogenic peptides that often have potent broad-spectrum antimicrobial activity, suggesting that antimicrobial and amyloidogenic peptides may represent two sides of the same coin. Here, we asked if the ability of an antifungal peptide to self-assemble affects its antifungal or antibacterial activity. We found that modifications of classical antifungal peptide derivative allowed it to self-assemble and did not alter its antifungal activity, and yet self-assembly substantially increased the antibacterial activity of the peptide. These results support the idea that peptide self-assembly can enhance antibacterial activities and emphasize a distinction between the action of antifungal peptides and that of antibacterial peptides. Accordingly, we suggest that the possible generality of this distinction should be widely tested.
抗药性病原菌的兴起唤起了人们对抗菌肽等新候选药物的兴趣,这些药物的衍生物也具有抗菌活性。最近的研究表明,某些抗菌肽能够自我组装成有序的淀粉样纳米结构,从而增强其抗菌活性。在这里,我们评估了一种基于组氨酸的抗菌肽及其自组装衍生物在自组装、膜相互作用以及抗菌和抗真菌活性之间的相互作用。我们证明了这两种肽都具有很强的膜靶向性,并且深入了解了这种作用机制,这与它们的抗真菌活性相关,不受其自组装状态的影响。然而,自组装的能力确实会显著影响肽对革兰氏阴性和革兰氏阳性细菌的抗菌活性。这些结果令人惊讶,暗示了抗真菌肽和抗菌肽在原核生物和真核微生物中的活性之间存在重要区别。抗菌肽是人类和其他多细胞生物抵抗细菌、真菌和病毒病原体的宿主防御的重要调节剂。两种趋同的范式表明,能够自我组装成类淀粉样纳米组装体的抗菌肽与通常具有强大广谱抗菌活性的经典淀粉样肽之间存在联系,这表明抗菌肽和淀粉样肽可能代表同一枚硬币的两面。在这里,我们想知道一种抗真菌肽的自组装能力是否会影响其抗真菌或抗菌活性。我们发现,经典抗真菌肽衍生物的修饰使其能够自我组装,并且不会改变其抗真菌活性,但自组装大大增加了肽的抗菌活性。这些结果支持了肽自组装可以增强抗菌活性的观点,并强调了抗真菌肽和抗菌肽作用之间的区别。因此,我们建议应该广泛测试这种区别的普遍性。