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Lipid interaction of Pseudomonas aeruginosa exotoxin A. Acid-triggered permeabilization and aggregation of lipid vesicles.

机译:铜绿假单胞菌外毒素A的脂质相互作用。酸触发脂质囊泡的透化和聚集。

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摘要

We have investigated the interaction of Pseudomonas exotoxin A with small unilamellar vesicles comprised of different phospholipids as a function of pH, toxin, and lipid concentration. We have found that this toxin induces vesicle permeabilization, as measured by the release of a fluorescent dye. Permeabilization is due to the formation of ion-conductive channels which we have directly observed in planar lipid bilayers. The toxin also produces vesicle aggregation, as indicated by an increase of the turbidity. Aggregation and permeabilization have completely different time course and extent upon toxin dose and lipid composition, thus suggesting that they are two independent events. Both time constants decrease by lowering the pH of the bulk phase or by introducing a negative lipid into the vesicles. Our results indicate that at least three steps are involved in the interaction of Pseudomonas exotoxin A with lipid vesicles. After protonation of one charged group the toxin becomes competent to bind to the surface of the vesicles. Binding is probably initiated by an electrostatic interaction because it is absolutely dependent on the presence of acidic phospholipids. Binding is a prerequisite for the subsequent insertion of the toxin into the lipid bilayer, with a special preference for phosphatidylglycerol-containing membranes, to form ionic channels. At high toxin and vesicle concentrations, bound toxin may also induce aggregation of the vesicles, particularly when phosphatidic acid is present in the lipid mixture. A quenching of the intrinsic tryptophan fluorescence of the protein, which is induced by lowering the pH of the solution, becomes more drastic in the presence of lipid vesicles. However, this further quenching takes so long that it cannot be a prerequisite to either vesicle permeabilization or aggregation. Pseudomonas exotoxin A shares many of these properties with other bacterial toxins like diphtheria and tetanus toxin.
机译:我们已经研究了假单胞菌外毒素A与小的单层囊泡的相互作用,囊泡由不同的磷脂组成,是pH,毒素和脂质浓度的函数。我们已经发现,该毒素诱导了囊泡通透化,如通过荧光染料的释放所测量的。通透性是由于我们在平面脂质双层中直接观察到的离子传导通道的形成。如浊度增加所示,毒素也产生囊泡聚集。聚集和通透性在毒素剂量和脂质组成上具有完全不同的时间过程和程度,因此表明它们是两个独立的事件。通过降低整体相的pH值或将负脂质引入囊泡,两种时间常数都会降低。我们的结果表明,假单胞菌外毒素A与脂质囊泡的相互作用至少涉及三个步骤。一个带电基团的质子化后,毒素变得能够结合囊泡表面。结合可能是由静电相互作用引发的,因为它绝对依赖于酸性磷脂的存在。结合是随后将毒素插入脂质双层的先决条件,特别优选含磷脂酰甘油的膜形成离子通道。在高毒素和囊泡浓度下,结合的毒素也可能诱导囊泡聚集,特别是当脂质混合物中存在磷脂酸时。在存在脂质囊泡的情况下,通过降低溶液的pH值诱导的蛋白质固有色氨酸荧光的猝灭变得更加剧烈。然而,这种进一步的淬灭花费了很长时间,以至于它既不是囊泡透化或聚集的先决条件。假单胞菌外毒素A与其他细菌毒素如白喉和破伤风毒素具有许多这些特性。

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