[揭示革兰氏阴性菌外膜的生物发生机制:迈向新抗生素开发的一步]。

J F Collet
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引用次数: 0

摘要

革兰氏阴性菌(如大肠杆菌)的外膜是一种渗透性屏障,对革兰氏阴性菌的生存能力至关重要,并保护它们免受包括疏水抗生素在内的抗菌药物的侵害。外膜成分,包括磷脂、脂多糖和蛋白质在细胞质和细胞质膜中合成。未折叠的蛋白质和脂质通过亲水周质转运并插入外膜的机制基本上是未知的。我们的总体目标是解决这样一个令人着迷的问题:如此复杂的大分子结构是如何在一个没有明显能量来源的隔间中组装起来的。此外,参与OM生物发生的蛋白质也是设计新的抗生素和抗炎药物的有吸引力的靶点。开发针对大肠杆菌和其他革兰氏阴性菌的新型抗生素至关重要,因为对抗生素具有耐药性的大肠杆菌菌株数量正在迅速增加。我们将描述最近在我们实验室获得的结果,这些结果使我们能够表征参与包膜蛋白折叠的几种质周伴侣。
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[Unravelling the mechanisms of the biogenesis of the outer membrane of Gram-negative bacteria: a step toward the development of new antibiotics].

The outer membrane of Gram negative bacteria such as Escherichia coli is a permeability barrier that is essential for the viability of Gram-negative bacteria and protects them against antimicrobial drugs, including hydrophobic antibiotics. Outer membrane components, including phospholipids, lipopolysaccharids and proteins are synthesized in the cytoplasm and the cytoplasmic membrane. The mechanisms by which unfolded proteins and lipids are then transported through the hydrophilic periplasm and are inserted in the outer membrane are essentially unknown. Our overall goal is to solve the fascinating problem of how such a complex macromolecular structure is assembled in a compartment devoid of obvious energy sources. Moreover, the proteins that are involved in OM biogenesis are also attractive targets for the design of new antibiotics and anti-inflammatory drugs. Developing new antibiotics active against E. coli and other Gram negative bacteria is criticial because the number of E. coli strains that are resistant to antibiotics is rapidly rising. We will describe results obtained recently in our laboratory that allowed us to characterize several periplasmic chaperones involved in the folding of envelope proteins.

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