Alving C R, Iglewski B H, Urban K A, Moss J, Richards R L, Sadoff J C
Proc Natl Acad Sci U S A. 1980 Apr;77(4):1986-90. doi: 10.1073/pnas.77.4.1986.
Diphtheria toxin bound to the phosphate portion of some, but not all, phospholipids in liposomes. Liposomes consisting of dimyristoyl phosphatidylcholine and cholesterol did not bind toxin. Addition of 20 mol% (compared to dimyristoyl phosphatidylcholine) of dipalmitoyl phosphatidic acid, dicetyl phosphate, phosphatidylinositol phosphate, cardiolipin, or phosphatidylserine in the liposomes resulted in substantial binding of toxin. Inclusion of phosphatidylinositol in dimyristol phosphatidylcholine/cholesterol liposomes did not result in toxin binding. The calcium salt of dipalmitoyl phosphatidic acid was more effective than the sodium salt, and the highest level of binding occurred with liposomes consisting only of dipalmitoyl phosphatidic acid (calcium salt) and cholesterol. Binding of toxin to liposomes was dependent on pH, and the pattern of pH dependence varied with liposomes having different compositions. Incubation of diphtheria toxin with liposomes containing dicetyl phosphate resulted in maximal binding at pH 3.6, whereas binding to liposomes containing phosphatidylinositol phosphate was maximal above pH 7. Toxin did not bind to liposomes containing 20 mol% of a free fatty acid (palmitic acid) or a sulfated lipid (3-sulfogalactosylceramide). Toxin binding to dicetyl phosphate or phosphatidylinositol phosphate was inhibited by UTP, ATP, phosphocholine, or p-nitrophenyl phosphate, but not by uracil. We conclude that (a) diphtheria toxin binds specifically to the phosphate portion of certain phospholipids, (b) binding to phospholipids in liposomes is dependent on pH, but is not due only to electrostatic interaction, and (c) binding may be strongly influenced by the composition of adjacent phospholipids that do not bind toxin. We propose that a minor membrane phospholipid (such as phosphatidylinositol phosphate or phosphatidic acid), or that some other phosphorylated membrane molecule (such as a phosphoprotein) may be important in the initial binding of diphtheria toxin to cells.
白喉毒素与脂质体中部分而非全部磷脂的磷酸部分结合。由二肉豆蔻酰磷脂酰胆碱和胆固醇组成的脂质体不结合毒素。在脂质体中添加20摩尔%(相对于二肉豆蔻酰磷脂酰胆碱)的二棕榈酰磷脂酸、十六烷基磷酸、磷脂酰肌醇磷酸、心磷脂或磷脂酰丝氨酸会导致毒素大量结合。在二肉豆蔻酰磷脂酰胆碱/胆固醇脂质体中加入磷脂酰肌醇不会导致毒素结合。二棕榈酰磷脂酸的钙盐比钠盐更有效,仅由二棕榈酰磷脂酸(钙盐)和胆固醇组成的脂质体结合水平最高。毒素与脂质体的结合取决于pH值,pH依赖性模式因脂质体组成不同而有所变化。白喉毒素与含有十六烷基磷酸的脂质体一起孵育,在pH 3.6时结合量最大,而与含有磷脂酰肌醇磷酸的脂质体结合在pH 7以上最大。毒素不与含有20摩尔%游离脂肪酸(棕榈酸)或硫酸化脂质(3 - 硫酸半乳糖神经酰胺)的脂质体结合。UTP、ATP、磷酸胆碱或对硝基苯磷酸可抑制毒素与十六烷基磷酸或磷脂酰肌醇磷酸的结合,但尿嘧啶无此作用。我们得出以下结论:(a)白喉毒素特异性结合某些磷脂的磷酸部分;(b)与脂质体中磷脂的结合取决于pH值,但不仅仅是由于静电相互作用;(c)结合可能受到不结合毒素的相邻磷脂组成的强烈影响。我们提出,一种少量的膜磷脂(如磷脂酰肌醇磷酸或磷脂酸),或某些其他磷酸化的膜分子(如磷蛋白)可能在白喉毒素与细胞的初始结合中起重要作用。