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The Design and Construction of K11: A Novel α-Helical Antimicrobial Peptide

机译:新型α-螺旋抗菌肽K11的设计与构建

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摘要

Amphipathic α-helical antimicrobial peptides comprise a class of broad-spectrum agents that are used against pathogens. We designed a series of antimicrobial peptides, CP-P (KWKSFIKKLTSKFLHLAKKF) and its derivatives, and determined their minimum inhibitory concentrations (MICs) against Pseudomonas aeruginosa, their minimum hemolytic concentrations (MHCs) for human erythrocytes, and the Therapeutic Index (MHC/MIC ratio). We selected the derivative peptide K11, which had the highest therapeutic index (320) among the tested peptides, to determine the MICs against Gram-positive and Gram-negative bacteria and 22 clinical isolates including Acinetobacter baumannii, methicillin-resistant Staphylococcus aureus, Pseudomonas aeruginosa, Staphylococcus epidermidis, and Klebsiella pneumonia. K11 exhibited low MICs (less than 10 μg/mL) and broad-spectrum antimicrobial activity, especially against clinically isolated drug-resistant pathogens. Therefore, these results indicate that K11 is a promising candidate antimicrobial peptide for further studies.
机译:两亲性α-螺旋抗菌肽包含一类用于抵抗病原体的广谱药物。我们设计了一系列抗菌肽CP-P(KWKSFIKKLTSKFLHLAKKF)及其衍生物,并确定了它们对铜绿假单胞菌的最低抑制浓度(MICs),对人红细胞的最低溶血浓度(MHCs)和治疗指数(MHC / MIC)比)。我们选择了在测试的多肽中具有最高治疗指数(320)的衍生肽K11来确定针对革兰氏阳性和革兰氏阴性细菌以及22种临床分离株的MIC,其中包括鲍曼不动杆菌,耐甲氧西林的金黄色葡萄球菌,铜绿假单胞菌,表皮葡萄球菌和肺炎克雷伯菌。 K11表现出低MIC(小于10μg/ mL)和广谱抗菌活性,尤其是针对临床分离的耐药病原体。因此,这些结果表明K11是有希望的候选抗微生物肽,用于进一步的研究。

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