Rapoport Iris, Boll Werner, Yu Anan, Böcking Till, Kirchhausen Tom
Department of Cell Biology and Immune Disease Institute, Harvard Medical School, Boston, MA 02115, USA.
Mol Biol Cell. 2008 Jan;19(1):405-13. doi: 10.1091/mbc.e07-09-0870. Epub 2007 Oct 31.
The 70-kDa heat-shock cognate protein (Hsc70) chaperone is an ATP-dependent "disassembly enzyme" for many subcellular structures, including clathrin-coated vesicles where it functions as an uncoating ATPase. Hsc70, and its cochaperone auxilin together catalyze coat disassembly. Like other members of the Hsp70 chaperone family, it is thought that ATP-bound Hsc70 recognizes the clathrin triskelion through an unfolded exposed hydrophobic segment. The best candidate is the unstructured C terminus (residues 1631-1675) of the heavy chain at the foot of the tripod below the hub, containing the sequence motif QLMLT, closely related to the sequence bound preferentially by the substrate groove of Hsc70 (Fotin et al., 2004b). To test this hypothesis, we generated in insect cells recombinant mammalian triskelions that in vitro form clathrin cages and clathrin/AP-2 coats exactly like those assembled from native clathrin. We show that coats assembled from recombinant clathrin are good substrates for ATP- and auxilin-dependent, Hsc70-catalyzed uncoating. Finally, we show that this uncoating reaction proceeds normally when the coats contain recombinant heavy chains truncated C-terminal to the QLMLT motif, but very inefficiently when the motif is absent. Thus, the QLMLT motif is required for Hsc-70-facilitated uncoating, consistent with the proposal that this sequence is a specific target of the chaperone.
70 kDa热休克同源蛋白(Hsc70)伴侣蛋白是一种依赖ATP的“拆解酶”,作用于许多亚细胞结构,包括网格蛋白包被小泡,在其中它作为去包被ATP酶发挥作用。Hsc70及其伴侣蛋白辅助蛋白共同催化包被的拆解。与Hsp70伴侣蛋白家族的其他成员一样,人们认为结合ATP的Hsc70通过一段未折叠的暴露疏水片段识别网格蛋白三脚蛋白复合体。最佳候选序列是位于枢纽下方三脚架底部重链的无结构C末端(第1631 - 1675位氨基酸残基),其包含序列基序QLMLT,与Hsc70底物凹槽优先结合的序列密切相关(Fotin等人,2004b)。为了验证这一假设,我们在昆虫细胞中生成了重组哺乳动物三脚蛋白复合体,其在体外形成的网格蛋白笼和网格蛋白/ AP - 2包被与由天然网格蛋白组装而成的完全一样。我们表明,由重组网格蛋白组装而成的包被是ATP和辅助蛋白依赖性、Hsc70催化去包被的良好底物。最后,我们表明,当包被包含在QLMLT基序C末端截短的重组重链时,这种去包被反应正常进行,但当该基序缺失时,反应效率极低。因此,QLMLT基序是Hsc - 70促进去包被所必需的,这与该序列是伴侣蛋白的特定靶标的提议一致。