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三磷酸肌醇磷脂与实验性变应性脑脊髓炎致病蛋白之间的复合物形成

Complex-formation between triphosphoinositide and experimental allergic encephalitogenic protein.

作者信息

Palmer F B, Dawson R M

出版信息

Biochem J. 1969 Mar;111(5):637-46.

Abstract
  1. Reactions between triphosphoinositide and the basic experimental allergic encephalitogenic (EAE) protein were examined in aqueous solution and in a biphasic solvent system (chloroform-methanol-water, 8:4:3, by vol.). 2. In the absence of salt an insoluble complex (I) is formed containing triphosphoinositide and EAE protein in proportions that represent complete neutralization of lipid and protein at the pH concerned. 3. In the presence of a low concentration (0.05m) of sodium chloride an insoluble positively charged complex (II) forms. It contains triphosphoinositide and EAE protein in a lower concentration ratio than complex I. This complex, which has a constant composition between pH7.5 and pH10, can take up additional micellar triphosphoinositide producing complex I, which can then be solubilized by excess of triphosphoinositide. 4. The complexes are dissociated by more concentrated sodium chloride solutions and low concentrations of calcium chloride, suggesting that they are largely stabilized by electrostatic bonds. The protein recovered after dissociation is immunologically active and has the same electrophoretic mobility as the original. 5. Water-insoluble ternary complexes containing triphosphoinositide, EAE protein and large amounts of phosphatidylcholine can be prepared. From these, chloroform-methanol (2:1, v/v) extracts only phosphatidylcholine. 6. An insoluble ternary complex of Ca(2+) ion, EAE protein and triphosphoinositide can be prepared by adding calcium chloride to a complex I preparation solubilized by excess of triphosphoinositide. 7. EAE protein will also form complexes with other acidic phospholipids, e.g. phosphatidic acid, phosphatidylserine and phosphatidylinositol, but not with phosphatidylcholine or phosphatidylethanolamine. The phosphatidylinositol and phosphatidylserine complexes are chloroform soluble, i.e. proteolipids. 8. The possibility that complexes between EAE protein and acidic phospholipids occur in vivo is discussed. Triphosphoinositide and EAE protein occur in ox brain myelin in approximately the same concentration ratios as they do in complex II, formed at physiological salt concentration and pH.
摘要
  1. 在水溶液和双相溶剂系统(氯仿 - 甲醇 - 水,体积比为8:4:3)中研究了三磷酸肌醇与碱性实验性变应性脑脊髓炎致病因(EAE)蛋白之间的反应。2. 在无盐的情况下,形成了一种不溶性复合物(I),其包含的三磷酸肌醇和EAE蛋白的比例在相关pH值下代表脂质和蛋白质的完全中和。3. 在低浓度(0.05m)氯化钠存在下,形成了一种带正电荷的不溶性复合物(II)。它所含的三磷酸肌醇和EAE蛋白的浓度比复合物I低。这种在pH7.5至pH10之间组成恒定的复合物可以摄取额外的胶束状三磷酸肌醇形成复合物I,然后可被过量的三磷酸肌醇溶解。4. 这些复合物会被更浓的氯化钠溶液和低浓度的氯化钙解离,这表明它们在很大程度上是由静电键稳定的。解离后回收的蛋白质具有免疫活性,并且电泳迁移率与原始蛋白质相同。5. 可以制备包含三磷酸肌醇、EAE蛋白和大量磷脂酰胆碱的水不溶性三元复合物。从这些复合物中,氯仿 - 甲醇(2:1,v/v)仅提取磷脂酰胆碱。6. 通过向用过量三磷酸肌醇溶解的复合物I制剂中加入氯化钙,可以制备钙(2 +)离子、EAE蛋白和三磷酸肌醇的不溶性三元复合物。7. EAE蛋白也会与其他酸性磷脂形成复合物,例如磷脂酸、磷脂酰丝氨酸和磷脂酰肌醇,但不会与磷脂酰胆碱或磷脂酰乙醇胺形成复合物。磷脂酰肌醇和磷脂酰丝氨酸复合物可溶于氯仿,即蛋白脂质。8. 讨论了EAE蛋白与酸性磷脂之间的复合物在体内发生的可能性。三磷酸肌醇和EAE蛋白在牛脑髓鞘中的浓度比与在生理盐浓度和pH值下形成的复合物II中的浓度比大致相同。

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