Department of Chemistry, Yonsei University, Seoul 03722, Republic of Korea.
ACS Nano. 2021 May 25;15(5):9143-9153. doi: 10.1021/acsnano.1c02644. Epub 2021 May 14.
Despite their high potency, the widespread implementation of natural antimicrobial peptides is still challenging due to their low scalability and high hemolytic activities. Herein, we address these issues by employing a modular approach to mimic the key amino acid residues present in antimicrobial peptides, such as lysine, leucine, and serine, but on the highly biocompatible poly(ethylene glycol) (PEG) backbone. A series of these PEG-based peptides (PEGtides) were developed using functional epoxide monomers, corresponding to each key amino acid, with several possessing highly potent bactericidal activities and controlled selectivities, with respect to their hemolytic behavior. The critical role of the composition and the structure of the PEGtides in their selectivities was further supported by coarse-grained molecular dynamic simulations. This modular approach is anticipated to provide the design principles necessary for the future development of antimicrobial polymers.
尽管它们具有高效力,但由于其低可扩展性和高溶血活性,天然抗菌肽的广泛应用仍然具有挑战性。在此,我们通过采用模块化方法来模拟抗菌肽中存在的关键氨基酸残基,如赖氨酸、亮氨酸和丝氨酸,但使用的是高度生物相容的聚乙二醇(PEG)主链。使用相应的功能环氧化物单体开发了一系列这些基于 PEG 的肽(PEGtides),每个单体对应一个关键氨基酸,其中一些具有高度有效的杀菌活性和选择性,相对于它们的溶血行为。粗粒度分子动力学模拟进一步支持了 PEGtides 的组成和结构在其选择性中的关键作用。这种模块化方法有望为未来抗菌聚合物的发展提供必要的设计原则。