Orci L, Stamnes M, Ravazzola M, Amherdt M, Perrelet A, Söllner T H, Rothman J E
Department of Morphology, Faculty of Medicine, University of Geneva Medical Center, Switzerland.
Cell. 1997 Jul 25;90(2):335-49. doi: 10.1016/s0092-8674(00)80341-4.
Electron microscope immunocytochemistry reveals that both anterograde-directed (proinsulin and VSV G protein) and retrograde-directed (the KDEL receptor) cargo are present in COPI-coated vesicles budding from every level of the Golgi stack in whole cells; however, they comprise two distinct populations that together can account for at least 80% of the vesicles budding from Golgi cisternae. Segregation of anterograde- from retrograde-directed cargo into distinct sets of COPI-coated vesicles is faithfully reproduced in the cell-free Golgi transport system, in which VSV G protein and KDEL receptor are packaged into separable vesicles, even when budding is driven by highly purified coatomer and a recombinant ARF protein.
电子显微镜免疫细胞化学显示,在全细胞中,从高尔基体堆栈各层芽生出的COPI被膜小泡中同时存在顺向运输的货物(胰岛素原和VSV G蛋白)和逆向运输的货物(KDEL受体);然而,它们构成两个不同的群体,共同至少占从高尔基池芽生出的小泡的80%。在无细胞高尔基体运输系统中,顺向运输与逆向运输的货物被分隔到不同的COPI被膜小泡中,这一过程得到了如实再现,在该系统中,即使出芽由高度纯化的外被体蛋白和重组ARF蛋白驱动,VSV G蛋白和KDEL受体也被包装到可分离的小泡中。