Wolf Dieter H, Hilt Wolfgang
Institut für Biochemie, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany.
Biochim Biophys Acta. 2004 Nov 29;1695(1-3):19-31. doi: 10.1016/j.bbamcr.2004.10.007.
The final destination of the majority of proteins that have to be selectively degraded in eukaryotic cells is the proteasome, a highly sophisticated nanomachine essential for life. 26S proteasomes select target proteins via their modification with polyubiquitin chains or, in rare cases, by the recognition of specific motifs. They are made up of different subcomplexes, a 20S core proteasome harboring the proteolytic active sites hidden within its barrel-like structure and two 19S caps that execute regulatory functions. Similar complexes equipped with PA28 regulators instead of 19S caps are a variation of this theme specialized for the production of antigenic peptides required in immune response. Structure analysis as well as extensive biochemical and genetic studies of the 26S proteasome and the ubiquitin system led to a basic model of substrate recognition and degradation. Recent work raised new concepts. Additional factors involved in substrate acquisition and delivery to the proteasome have been discovered. Moreover, first insights in the tasks of individual subunits or subcomplexes of the 19S caps in substrate recognition and binding as well as release and recycling of polyubiquitin tags have been obtained.
在真核细胞中,大多数需要被选择性降解的蛋白质的最终归宿是蛋白酶体,这是一种对生命至关重要的高度复杂的纳米机器。26S蛋白酶体通过多聚泛素链修饰来选择靶蛋白,在极少数情况下,也通过识别特定基序来选择。它们由不同的亚复合物组成,一个20S核心蛋白酶体,其蛋白水解活性位点隐藏在桶状结构内,还有两个执行调节功能的19S帽。配备PA28调节因子而非19S帽的类似复合物是这一主题的变体,专门用于产生免疫反应所需的抗原肽。对26S蛋白酶体和泛素系统的结构分析以及广泛的生化和遗传学研究得出了底物识别和降解的基本模型。最近的研究提出了新的概念。已发现参与底物获取和向蛋白酶体递送的其他因素。此外,还首次深入了解了19S帽的各个亚基或亚复合物在底物识别和结合以及多聚泛素标签的释放和循环利用中的任务。