Lai C S, Kushnaryov V, Panz T, Basosi R
Arch Biochem Biophys. 1984 Oct;234(1):1-6. doi: 10.1016/0003-9861(84)90317-5.
Diphtheria toxin (DT) induces the leakage of dipalmitoylphosphatidic acid (DPPA) membranes but not neutral dipalmitoylphosphatidylcholine (DPPC) membranes. Cholesterol incorporated into liposomes enhances the membrane leakage induced by DT in acidic DPPA membranes but not in neutral DPPC membranes. Membrane leakage was determined by assaying the release of TEMPOcholine, a cationic spin probe from the multilamellar vesicles by using electron spin resonance methods. The effect of DT on membrane leakage is noticeable at 3 micrograms/ml concentrations, and reaches a plateau of about 20% leakage at 20 micrograms/ml. This saturation phenomenon led to the postulation that DT binds to the first shell of DPPA membranes and induces the leakage of TEMPOcholine limited to this layer of DPPA multimellar vesicles.
白喉毒素(DT)可诱导二棕榈酰磷脂酸(DPPA)膜泄漏,但不会导致中性二棕榈酰磷脂酰胆碱(DPPC)膜泄漏。掺入脂质体的胆固醇会增强DT在酸性DPPA膜中诱导的膜泄漏,但在中性DPPC膜中则不会。通过使用电子自旋共振方法测定阳离子自旋探针TEMPO胆碱从多层囊泡中的释放来确定膜泄漏情况。DT对膜泄漏的影响在浓度为3微克/毫升时较为明显,在20微克/毫升时达到约20%泄漏的平台期。这种饱和现象导致推测DT与DPPA膜的第一层结合,并诱导限于这层DPPA多层囊泡的TEMPO胆碱泄漏。