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Real-time attack on single Escherichia coli cells by the human antimicrobial peptide LL-37

机译:人类抗菌肽LL-37对单个大肠杆菌细胞的实时攻击

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摘要

Natural antimicrobial peptides (AMPs) provide prototypes for the design of unconventional antimicrobial agents. Existing bulk assays measure AMP activity but do not provide details of the growth-halting mechanism. We use fluorescence microscopy to directly observe the attack of the human antimicrobial peptide LL-37 on single Escherichia coli cells in real time. Our findings strongly suggest that disruption of the cytoplasmic membrane is not the growth-halting mechanism. At 8 μM, LL-37 binding saturates the outer membrane (OM) within 1 min. Translocation across the OM and access to the periplasmic space (5–25 min later) correlates in time with the halting of growth. Septating cells are attacked more readily than nonseptating cells. The halting of growth may occur because of LL-37 interference with cell wall biogenesis. Only well after growth halts does the peptide permeabilize the cytoplasmic membrane to GFP and the small dye Sytox Green. The assay enables dissection of antimicrobial design criteria into two parts: translocation across the OM and the subsequent halting of growth.
机译:天然抗菌肽(AMPs)为非常规抗菌剂的设计提供了原型。现有的大量测定法可测量AMP活性,但未提供阻止生长机制的详细信息。我们使用荧光显微镜直接实时观察人类抗菌肽LL-37对单个大肠杆菌细胞的攻击。我们的发现强烈暗示细胞质膜的破坏不是生长停止机制。在8μM下,LL-37结合会在1分钟内使外膜(OM)饱和。跨越OM的易位和进入周质空间的时间(5–25分钟后)与生长的停止时间相关。隔离细胞比非隔离细胞更容易受到攻击。可能由于LL-37干扰细胞壁生物发生而停止生长。生长停止后,肽才能很好地将细胞质膜通透至GFP和小染料Sytox Green。该测定法可将抗微生物设计标准分为两部分:穿过OM的易位和随后的生长停止。

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