Sato K, Wickner W
Dartmouth Medical School, Department of Biochemistry, Hanover, NH 03755-3844, USA.
Science. 1998 Jul 31;281(5377):700-2. doi: 10.1126/science.281.5377.700.
Membrane trafficking has heretofore been studied with intact organelles. Here, fusion-competent proteoliposomes were reconstituted from a yeast vacuole detergent extract. Homotypic vacuole fusion requires many membrane proteins, including the Ypt7p guanosine triphosphatase and a "SNARE complex" with Vam3p and Nyv1p. Proteoliposomes from extracts immunodepleted of either Vam3p or Ypt7p could not fuse, but vesicles reconstituted from a mixture of these depleted extracts had restored fusion activity. Purified preassembled vacuolar SNARE complex, when reconstituted with a SNARE-depleted extract, was fully functional for fusion. Thus, solubilized integral membrane components can be reconstituted for priming, docking, and fusion steps of organelle trafficking.
迄今为止,膜运输一直是通过完整的细胞器进行研究的。在这里,有融合能力的蛋白脂质体是从酵母液泡去污剂提取物中重构出来的。同型液泡融合需要许多膜蛋白,包括Ypt7p鸟苷三磷酸酶和与Vam3p和Nyv1p组成的“可溶性N-乙基马来酰胺敏感因子附着蛋白受体复合体”。来自免疫去除了Vam3p或Ypt7p的提取物的蛋白脂质体无法融合,但由这些去除提取物的混合物重构的囊泡恢复了融合活性。纯化的预组装液泡可溶性N-乙基马来酰胺敏感因子附着蛋白受体复合体,当与去除了可溶性N-乙基马来酰胺敏感因子附着蛋白受体的提取物重构时,对融合具有完全功能。因此,溶解的整合膜成分可以被重构用于细胞器运输的引发、对接和融合步骤。