Menestrina G, Pederzolli C, Forti S, Gambale F
Dipartimento di Fisica, Università di Trento, Italy.
Biophys J. 1991 Dec;60(6):1388-400. doi: 10.1016/S0006-3495(91)82176-2.
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.
我们研究了绿脓杆菌外毒素A与由不同磷脂组成的小单层囊泡之间的相互作用,该相互作用是pH值、毒素和脂质浓度的函数。我们发现,这种毒素可诱导囊泡通透性增加,这可通过荧光染料的释放来测量。通透性增加是由于形成了离子传导通道,我们已在平面脂质双分子层中直接观察到这些通道。毒素还会导致囊泡聚集,这可通过浊度增加来表明。聚集和通透性增加在毒素剂量和脂质组成方面具有完全不同的时间进程和程度,因此表明它们是两个独立的事件。通过降低本体相的pH值或向囊泡中引入带负电荷的脂质,两个时间常数都会减小。我们的结果表明,绿脓杆菌外毒素A与脂质囊泡的相互作用至少涉及三个步骤。一个带电基团质子化后,毒素就能够与囊泡表面结合。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。结合是毒素随后插入脂质双分子层的先决条件,毒素特别倾向于插入含有磷脂酰甘油的膜中以形成离子通道。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。溶液pH值降低会诱导蛋白质内在色氨酸荧光猝灭,在脂质囊泡存在的情况下这种猝灭会更加剧烈。然而,这种进一步的猝灭所需时间很长,因此它不可能是囊泡通透性增加或聚集的先决条件。绿脓杆菌外毒素A与其他细菌毒素如白喉毒素和破伤风毒素具有许多这些共同特性。