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The development of antimicrobial γ-AApeptides

机译:抗菌γ-AA肽的发展

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摘要

Host-defense peptides (HDPs) are promising next generation of antibiotic agents, as they have the potential to circumvent emerging drug resistance, due to their mechanism of bacterial killing through disruption of their membranes. Nonetheless, HDPs have intrinsic drawbacks such as low-to-moderate activity, susceptibility to enzymatic degradation. In the past few years, we developed a new class of peptidomimetics named ‘γ-AApeptides’, which have superior resistance to proteolysis and a variety of diversification via straightforward synthesis. Our recent studies suggested that γ-AApeptides can mimic the bactericidal mechanism of HDPs and show potent and broad-spectrum activity against both Gram-positive and Gram-negative multidrug-resistant bacteria. In this review, we summarize our current studies of antimicrobial γ-AApeptides and discuss their potential future development as antimicrobial peptidomimetics.
机译:宿主防御肽(HDP)有望成为下一代抗生素,因为它们具有通过破坏其膜而杀死细菌的机制,因此有可能规避新兴的耐药性。但是,HDP具有内在的缺点,例如活性低至中等,对酶促降解的敏感性。在过去的几年中,我们开发了一种新型的肽模拟物,称为“γ-AA肽”,通过直接合成,它们具有出色的抗蛋白水解性和多种多样化的能力。我们最近的研究表明,γ-AA肽可以模仿HDP的杀菌机制,并显示出对革兰氏阳性和革兰氏阴性多药耐药细菌的有效和广谱活性。在这篇综述中,我们总结了目前对抗菌素γ-AA​​肽的研究,并讨论了其作为抗菌肽模拟物的潜在未来发展。

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