Hannan L A, Newmyer S L, Schmid S L
Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Mol Biol Cell. 1998 Aug;9(8):2217-29. doi: 10.1091/mbc.9.8.2217.
Clathrin-coated vesicles (CCV) mediate protein sorting and vesicular trafficking from the plasma membrane and the trans-Golgi network. Before delivery of the vesicle contents to the target organelles, the coat components, clathrin and adaptor protein complexes (APs), must be released. Previous work has established that hsc70/the uncoating ATPase mediates clathrin release in vitro without the release of APs. AP release has not been reconstituted in vitro, and nothing is known about the requirements for this reaction. We report a novel quantitative assay for the ATP- and cytosol- dependent release of APs from CCV. As expected, hsc70 is not sufficient for AP release; however, immunodepletion and reconstitution experiments establish that it is necessary. Interestingly, complete clathrin release is not a prerequisite for AP release, suggesting that hsc70 plays a dual role in recycling the constituents of the clathrin coat. This assay provides a functional basis for identification of the additional cytosolic factor(s) required for AP release.
网格蛋白包被小泡(CCV)介导从质膜和反式高尔基体网络进行的蛋白质分选和小泡运输。在将小泡内容物递送至靶细胞器之前,包被成分,即网格蛋白和衔接蛋白复合物(APs),必须被释放。先前的研究已经证实,hsc70/去包被ATP酶在体外介导网格蛋白的释放,但不释放APs。AP的释放尚未在体外重建,对于该反应的需求也一无所知。我们报道了一种新的定量测定方法,用于从CCV中ATP和胞质溶胶依赖性释放APs。正如预期的那样,hsc70不足以释放APs;然而,免疫耗竭和重建实验表明它是必需的。有趣的是,完全释放网格蛋白不是释放AP的先决条件,这表明hsc70在回收网格蛋白包被的成分中起双重作用。该测定为鉴定AP释放所需的其他胞质因子提供了功能基础。