Helenius A, Sarvas M, Simons K
Eur J Biochem. 1981 May;116(1):27-35. doi: 10.1111/j.1432-1033.1981.tb05296.x.
The dissociation and reconstitution of the Semliki Forest virus membrane using the nonionic detergent octyl beta-D-glucoside was studied by sucrose density gradient centrifugation. The dissociation occurred in three stages: lysis at a free equilibrium octyl glucoside concentration of 14--18 mM, solubilization at 18--20 mM, and delipidation of the spike glycoproteins at the critical micellar concentration (22 mM) or higher. After solubilization the spike glycoproteins were present as soluble complexes with sedimentation coefficients of 19 S and 6 S. The 6-S form probably corresponded to a glycoprotein monomer complexed to detergent and the 19-S form consisted of oligomeric detergent-protein complexes. The two forms were in slow equilibrium with each other. When the soluble spike protein complexes and egg lecithin solubilized with octyl glucoside were mixed and the octyl glucoside concentration lowered either by dialysis or by dilution, reconstitution occurred. Three types of products were obtained: vesicles with 30% of the spike protein facing inwards and 70% facing outwards, vesicles with virtually all (95%) of the spike proteins pointing outwards, and small protein-rich soluble aggregates [Helenius et al. (1977) J. Cell Biol. 75, 866]. It was demonstrated that during reconstitution the symmetric vesicles were formed at 19 mM free equilibrium octyl glucoside by the association of the 6-S protein complexes with the phospholipids, and the asymmetric vesicles were formed at 10--16 mM octyl glucoside when the 19-S complexes associated with the lipids. Asymmetric membrane vesicles were also obtained when membrane penicillinase from Bacillus licheniformis was reconstituted with egg lecithin using octyl glucoside. It could be shown that the penicillinase was oligomeric at the octyl glycoside concentration where the reconstitution occurred. The results demonstrate that different mechanisms of reconstitution give rise to the symmetric and the asymmetric vesicles. The critical factor in determining the mechanism is the state of aggregation of the proteins at the octyl glucoside concentration where membranes begin to form from the solubilized lipids.
利用非离子去污剂辛基-β-D-葡萄糖苷对Semliki森林病毒膜进行解离和重组,通过蔗糖密度梯度离心法进行研究。解离过程分三个阶段:在游离平衡辛基葡萄糖苷浓度为14 - 18 mM时发生裂解,18 - 20 mM时发生溶解,在临界胶束浓度(22 mM)或更高浓度时刺突糖蛋白发生脱脂。溶解后,刺突糖蛋白以沉降系数为19 S和6 S的可溶性复合物形式存在。6-S形式可能对应于与去污剂复合的糖蛋白单体,19-S形式由寡聚去污剂-蛋白复合物组成。这两种形式相互间处于缓慢平衡状态。当将可溶性刺突蛋白复合物与用辛基葡萄糖苷溶解的卵磷脂混合,并通过透析或稀释降低辛基葡萄糖苷浓度时,就会发生重组。得到了三种类型的产物:30%的刺突蛋白向内、70%向外的囊泡,几乎所有(95%)刺突蛋白都向外的囊泡,以及富含蛋白质的小可溶性聚集体[海伦纽斯等人(1977年)《细胞生物学杂志》75卷,866页]。结果表明,在重组过程中,6-S蛋白复合物与磷脂结合,在游离平衡辛基葡萄糖苷浓度为19 mM时形成对称囊泡,而19-S复合物与脂质结合时,在辛基葡萄糖苷浓度为10 - 16 mM时形成不对称囊泡。当用辛基葡萄糖苷将地衣芽孢杆菌的膜青霉素酶与卵磷脂重组时,也获得了不对称膜囊泡。可以证明,在发生重组的辛基糖苷浓度下,青霉素酶是寡聚体。结果表明,不同的重组机制产生了对称和不对称囊泡。决定重组机制的关键因素是在从溶解的脂质开始形成膜的辛基葡萄糖苷浓度下蛋白质的聚集状态。