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Probing the Penetration of Antimicrobial Polymyxin Lipopeptides into Gram-Negative Bacteria

机译:探究抗细菌多粘菌素脂肽向革兰氏阴性细菌的渗透

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The dry antibiotic development pipeline coupled with the emergence of multidrug resistant Gram-negative 'superbugs' has driven the revival of the polymyxin lipopeptide antibiotics. Polymyxin resistance implies a total lack of antibiotics for the treatment of life-threatening infections. The lack of molecular imaging probes that possess native polymyxin-like antibacterial activity is a barrier to understanding the resistance mechanisms and the development of a new generation of polymyxin lipopeptides. Here we report the regioselective modification of the polymyxin B core scaffold at the N-terminus with the dansyl fluorophore to generate an active probe that mimics polymyxin B pharmacologically. Time-lapse laser scarming confocal microscopy imaging of the penetration of probe (1) into Gram-negative bacterial cells revealed that the probe initially accumulates in the outer membrane and subsequently penetrates into the inner membrane and finally the cytoplasm. The implementation of this polymyxin-mimetic probe will advance the development of platforms for the discovery of novel polymyxin lipopeptides with efficacy against polymyxin-resistant strains.
机译:干燥的抗生素开发流程以及对多药耐药的革兰氏阴性“超级细菌”的出现推动了多粘菌素脂肽抗生素的复兴。多粘菌素耐药性意味着完全没有抗生素可以治疗威胁生命的感染。缺乏具有天然多粘菌素样抗菌活性的分子成像探针是理解耐药机制和新一代多粘菌素脂肽发展的障碍。在这里,我们报告在丹尼斯基荧光团在N末端的多粘菌素B核心支架的区域选择性修饰,以产生药理学上模仿多粘菌素B的活性探针。探针(1)渗透到革兰氏阴性细菌细胞中的延时激光疤痕共聚焦显微镜成像表明,该探针最初聚集在外膜中,然后渗入内膜,最后渗入细胞质。该多粘菌素模拟物探针的实施将促进用于发现具有抗多粘菌素抗性菌株的功效的新型多粘菌素脂肽的平台的开发。

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