Madura Kiran
Robert Wood Johnson Medical School, Department of Biochemistry, 683 Hoes Lane, Piscataway, NJ 08854, USA.
Trends Biochem Sci. 2004 Dec;29(12):637-40. doi: 10.1016/j.tibs.2004.10.008.
Substrate ubiquitination is highly regulated; by contrast, substrate targeting to the proteasome has been considered a stochastic process that is mediated primarily by high-affinity interaction with multi-ubiquitin chains. However, recent findings have shown that substrate recognition by the proteasome is also regulated, and requires Rad23, Dsk2 and Rpn10. These studies suggest that the engagement of protein ubiquitination and translocation with degradation by the proteasome is coordinated by a series of regulated events.
底物泛素化受到高度调控;相比之下,底物靶向蛋白酶体一直被认为是一个随机过程,主要由与多聚泛素链的高亲和力相互作用介导。然而,最近的研究结果表明,蛋白酶体对底物的识别也是受到调控的,并且需要Rad23、Dsk2和Rpn10。这些研究表明,蛋白质泛素化和转运与蛋白酶体降解的衔接是由一系列受调控的事件协调的。