Department of Chemistry and Biochemistry, Center for Biomolecular Structure and Organization, University of Maryland, College Park, Maryland, USA.
Department of Chemistry and Biochemistry, Center for Biomolecular Structure and Organization, University of Maryland, College Park, Maryland, USA.
J Biol Chem. 2021 Jan-Jun;296:100450. doi: 10.1016/j.jbc.2021.100450. Epub 2021 Feb 20.
Proteasome-mediated substrate degradation is an essential process that relies on the coordinated actions of ubiquitin (Ub), shuttle proteins containing Ub-like (UBL) domains, and the proteasome. Proteinaceous substrates are tagged with polyUb and shuttle proteins, and these signals are then recognized by the proteasome, which subsequently degrades the substrate. To date, three proteasomal receptors have been identified, as well as multiple shuttle proteins and numerous types of polyUb chains that signal for degradation. While the components of this pathway are well-known, our understanding of their interplay is unclear-especially in the context of Rpn1, the largest proteasomal subunit. Here, using nuclear magnetic resonance (NMR) spectroscopy in combination with competition assays, we show that Rpn1 associates with UBL-containing proteins and polyUb chains, while exhibiting a preference for shuttle protein Rad23. Rpn1 appears to contain multiple Ub/UBL-binding sites, theoretically as many as one for each of its hallmark proteasome/cyclosome repeats. Remarkably, we also find that binding sites on Rpn1 can be shared among Ub and UBL species, while proteasomal receptors Rpn1 and Rpn10 can compete with each other for binding of shuttle protein Dsk2. Taken together, our results rule out the possibility of exclusive recognition sites on Rpn1 for individual Ub/UBL signals and further emphasize the complexity of the redundancy-laden proteasomal degradation pathway.
蛋白酶体介导的底物降解是一个基本过程,依赖于泛素 (Ub)、含有泛素样 (UBL) 结构域的穿梭蛋白以及蛋白酶体的协调作用。蛋白质底物被多泛素化和穿梭蛋白标记,这些信号随后被蛋白酶体识别,随后降解底物。迄今为止,已经鉴定出三种蛋白酶体受体,以及多种穿梭蛋白和多种类型的多泛素链,这些信号用于降解。虽然该途径的组成部分是众所周知的,但我们对它们相互作用的理解尚不清楚——尤其是在 Rpn1(最大的蛋白酶体亚基)的背景下。在这里,我们使用核磁共振 (NMR) 光谱结合竞争测定,表明 Rpn1 与含有 UBL 的蛋白质和多泛素链结合,同时表现出对穿梭蛋白 Rad23 的偏好。Rpn1 似乎包含多个 Ub/UBL 结合位点,理论上每个标志性的蛋白酶体/环化酶重复都有一个结合位点。值得注意的是,我们还发现 Rpn1 上的结合位点可以在 Ub 和 UBL 物种之间共享,而蛋白酶体受体 Rpn1 和 Rpn10 可以相互竞争结合穿梭蛋白 Dsk2。总之,我们的结果排除了 Rpn1 上单个 Ub/UBL 信号的特有识别位点的可能性,并进一步强调了富含冗余的蛋白酶体降解途径的复杂性。