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纯化衔接蛋白在体外对胞质溶胶和网格蛋白依赖的内吞作用的刺激。

Cytosol- and clathrin-dependent stimulation of endocytosis in vitro by purified adaptors.

作者信息

Smythe E, Carter L L, Schmid S L

机构信息

Department of Cell Biology, Scripps Research Institute, La Jolla, California 92037.

出版信息

J Cell Biol. 1992 Dec;119(5):1163-71. doi: 10.1083/jcb.119.5.1163.

Abstract

Using stage-specific assays for receptor-mediated endocytosis of transferrin (Tfn) into perforated A431 cells we show that purified adaptors stimulate coated pit assembly and ligand sequestration into deeply invaginated coated pits. Late events in endocytosis involving membrane fission and coated vesicle budding which lead to the internalization of Tfn are unaffected. AP2, plasma membrane adaptors, are active at physiological concentrations, whereas AP1, Golgi adaptors, are inactive. Adaptor-dependent stimulation of Tfn sequestration requires cytosolic clathrin, but is unaffected by clathrin purified from coated vesicles suggesting that soluble and assembled clathrin pools are functionally distinct. In addition to adaptors and cytosolic clathrin other, as yet unidentified, cytosolic factors are also required for efficient coated pit invagination. These results provide new insight into the mechanisms and regulation of coated pit assembly and invagination.

摘要

利用针对转铁蛋白(Tfn)通过受体介导的内吞作用进入穿孔A431细胞的阶段特异性检测方法,我们发现纯化的衔接蛋白可刺激包被小窝组装,并将配体隔离到深陷的包被小窝中。内吞作用中涉及膜裂变和包被囊泡出芽从而导致Tfn内化的后期事件不受影响。质膜衔接蛋白AP2在生理浓度下具有活性,而高尔基体衔接蛋白AP1则无活性。衔接蛋白依赖性的Tfn隔离刺激需要胞质网格蛋白,但不受从包被囊泡中纯化的网格蛋白的影响,这表明可溶性和组装好的网格蛋白池在功能上是不同的。除了衔接蛋白和胞质网格蛋白外,高效的包被小窝内陷还需要其他尚未确定的胞质因子。这些结果为包被小窝组装和内陷的机制及调控提供了新的见解。

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