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网格蛋白包被小窝从质膜出芽的重建。

Reconstitution of clathrin-coated pit budding from plasma membranes.

作者信息

Lin H C, Moore M S, Sanan D A, Anderson R G

机构信息

Department of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235-9039.

出版信息

J Cell Biol. 1991 Sep;114(5):881-91. doi: 10.1083/jcb.114.5.881.

Abstract

Receptor-mediated endocytosis begins with the binding of ligand to receptors in clathrin-coated pits followed by the budding of the pits away from the membrane. We have successfully reconstituted this sequence in vitro. Highly purified plasma membranes labeled with gold were obtained by incubating cells in the presence of anti-LDL receptor IgG-gold at 4 degrees C, attaching the labeled cells to a poly-L-lysine-coated substratum at 4 degrees C and then gently sonicating them to remove everything except the adherent membrane. Initially the gold label was clustered over flat, clathrin-coated pits. After these membranes were warmed to 37 degrees C for 5-10 min in the presence of buffer that contained cytosol extract, Ca2+, and ATP, the coated pits rounded up and budded from the membrane, leaving behind a membrane that was devoid of LDL gold. Simultaneous with the loss of the ligand, the clathrin triskelion and the AP-2 subunits of the coated pit were also lost. These results suggest that the budding of a coated pit to form a coated vesicle occurs in two steps: (a) the spontaneous rounding of the flat lattice into a highly invaginated coated pit at 37 degrees C; (b) the ATP, 150 microM Ca2+, and cytosolic factors(s) dependent fusion of the adjoining membrane segments at the neck of the invaginated pit.

摘要

受体介导的内吞作用始于配体与网格蛋白包被小窝中的受体结合,随后小窝从膜上出芽。我们已在体外成功重建了这一过程。通过在4℃下于抗低密度脂蛋白(LDL)受体IgG-金存在的情况下孵育细胞,将标记的细胞在4℃下附着于聚-L-赖氨酸包被的基质上,然后轻轻超声处理以除去除附着膜之外的所有物质,从而获得用金标记的高度纯化的质膜。最初,金标记聚集在扁平的、网格蛋白包被的小窝上。在含有胞质溶胶提取物、Ca2+和ATP的缓冲液存在下,将这些膜在37℃温育5-10分钟后,包被小窝变圆并从膜上出芽,留下不含LDL金的膜。与配体丧失同时,包被小窝的网格蛋白三脚复合体和AP-2亚基也丧失。这些结果表明,包被小窝出芽形成包被囊泡分两步进行:(a)在37℃下扁平晶格自发变圆形成高度内陷的包被小窝;(b)ATP、150μM Ca2+和胞质因子依赖的内陷小窝颈部相邻膜段的融合。

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