Elsasser Suzanne, Finley Daniel
Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.
Nat Cell Biol. 2005 Aug;7(8):742-9. doi: 10.1038/ncb0805-742.
Recent work has shown that ubiquitination leads to recognition of target proteins by diverse ubiquitin receptors. One family of receptors delivers the ubiquitinated proteins to the proteasome resulting in ATP-dependent substrate unfolding and proteolysis. A related family of ubiquitin-binding proteins seems to recruit ubiquitinated proteins to Cdc48, an ATPase ring complex that can also unfold proteins. Some targets seem to dock at Cdc48 before the proteasome does, in an ordered pathway. The intimate interplay between the proteasome and Cdc48, mediated in part by loosely associated ubiquitin receptors, has important functions in cellular regulation.
近期研究表明,泛素化作用可使多种泛素受体识别靶蛋白。其中一类受体将泛素化蛋白传递至蛋白酶体,从而导致依赖ATP的底物解折叠及蛋白水解。一类与之相关的泛素结合蛋白似乎可将泛素化蛋白招募至Cdc48,Cdc48是一种同样能够使蛋白解折叠的ATP酶环复合物。一些靶蛋白似乎在蛋白酶体之前,按有序途径停靠于Cdc48。蛋白酶体与Cdc48之间的密切相互作用,部分由松散结合的泛素受体介导,在细胞调节中具有重要作用。