Ferrell K, Wilkinson C R, Dubiel W, Gordon C
Dept of Biochemistry, University of Utah, 50 N. Medical Drive, Salt Lake City, UT 84132, USA.
Trends Biochem Sci. 2000 Feb;25(2):83-8. doi: 10.1016/s0968-0004(99)01529-7.
The 26S proteasome is the major non-lysosomal protease in eukaryotic cells. This multimeric enzyme is the integral component of the ubiquitin-mediated substrate degradation pathway. It consists of two subcomplexes, the 20S proteasome, which forms the proteolytic core, and the 19S regulator (or PA700), which confers ATP dependency and ubiquitinated substrate specificity on the enzyme. Recent biochemical and genetic studies have revealed many of the interactions between the 17 regulatory subunits, yielding an approximation of the 19S complex topology. Inspection of interactions of regulatory subunits with non-subunit proteins reveals patterns that suggest these interactions play a role in 26S proteasome regulation and localization.
26S蛋白酶体是真核细胞中主要的非溶酶体蛋白酶。这种多聚体酶是泛素介导的底物降解途径的重要组成部分。它由两个亚复合物组成,即形成蛋白水解核心的20S蛋白酶体和赋予该酶ATP依赖性及泛素化底物特异性的19S调节因子(或PA700)。最近的生化和遗传学研究揭示了17个调节亚基之间的许多相互作用,从而对19S复合物的拓扑结构有了大致了解。对调节亚基与非亚基蛋白相互作用的研究揭示了一些模式,表明这些相互作用在26S蛋白酶体的调节和定位中发挥作用。