Antimicrobial Peptides Based on Bacterial S1 Protein Sequences as a Potential Alternative to Antibiotics

O. Galzitskaya, A. Machulin, E. I. Deryusheva, A. Glyakina, S. Grishin, S. Kurpe, A. V. Panfilov, P. Domnin, S. V. Kravchenko, S. Ermolaeva
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Abstract

An original approach to the development of antimicrobial peptides (AMPs) with a new mechanism of action based on directed coaggregation of a peptide with a target protein is proposed. The unique multifunctional bacterial ribosomal protein S1 was chosen as the target protein. The amyloidogenic and antibacterial effects of various peptides synthesized on the basis of S1 ribosomal protein sequences were studied. The results obtained can serve as a basis for the creation of new AMPs against various strains of pathogenic organisms.
基于细菌S1蛋白序列的抗菌肽作为抗生素的潜在替代品
本文提出了一种基于肽与靶蛋白定向共聚集的新型抗菌肽(AMPs)的开发方法。选择独特的多功能细菌核糖体蛋白S1作为靶蛋白。研究了基于S1核糖体蛋白序列合成的多种多肽的淀粉样蛋白生成和抗菌作用。所得结果可作为制备抗多种病原菌菌株的新抗菌肽的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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