Walters Kylie J, Goh Amanda M, Wang Qinghua, Wagner Gerhard, Howley Peter M
Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, MN 55455, USA.
Biochim Biophys Acta. 2004 Nov 29;1695(1-3):73-87. doi: 10.1016/j.bbamcr.2004.10.005.
Many biological processes rely on targeted protein degradation, the dysregulation of which contributes to the pathogenesis of various diseases. Ubiquitin plays a well-established role in this process, in which the covalent attachment of polyubiquitin chains to protein substrates culminates in their degradation via the proteasome. The three-dimensional structural topology of ubiquitin is highly conserved as a domain found in a variety of proteins of diverse biological function. Some of these so-called "ubiquitin family proteins" have recently been shown to bind components of the 26S proteasome via their ubiquitin-like domains, thus implicating proteasome activity in pathways other than protein degradation. In this chapter, we provide a structural perspective of how the ubiquitin family of proteins interacts with the proteasome.
许多生物过程依赖于靶向蛋白质降解,其失调会导致各种疾病的发病机制。泛素在这一过程中发挥着既定作用,其中多聚泛素链与蛋白质底物的共价连接最终导致它们通过蛋白酶体降解。泛素的三维结构拓扑作为一个结构域高度保守,存在于多种具有不同生物学功能的蛋白质中。最近发现,其中一些所谓的“泛素家族蛋白”可通过其类泛素结构域与26S蛋白酶体的组分结合,从而表明蛋白酶体活性参与了蛋白质降解以外的其他途径。在本章中,我们从结构角度阐述了泛素家族蛋白如何与蛋白酶体相互作用。