Department of Molecular Biosciences, Northwestern University, Evanston, Illinois 60208, USA.
1] Department of Molecular Biosciences, Northwestern University, Evanston, Illinois 60208, USA. [2] Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, Texas 78712, USA.
Nat Rev Mol Cell Biol. 2014 Feb;15(2):122-33. doi: 10.1038/nrm3741.
The ubiquitin proteasome system (UPS) is the main ATP-dependent protein degradation pathway in the cytosol and nucleus of eukaryotic cells. At its centre is the 26S proteasome, which degrades regulatory proteins and misfolded or damaged proteins. In a major breakthrough, several groups have determined high-resolution structures of the entire 26S proteasome particle in different nucleotide conditions and with and without substrate using cryo-electron microscopy combined with other techniques. These structures provide some surprising insights into the functional mechanism of the proteasome and will give invaluable guidance for genetic and biochemical studies of this key regulatory system.
泛素蛋白酶体系统 (UPS) 是真核细胞细胞质和细胞核中主要的依赖于 ATP 的蛋白质降解途径。其核心是 26S 蛋白酶体,它可降解调节蛋白和错误折叠或受损的蛋白质。在一项重大突破中,几个研究小组使用冷冻电镜结合其他技术,在不同核苷酸条件下以及有和没有底物的情况下,确定了整个 26S 蛋白酶体颗粒的高分辨率结构。这些结构为蛋白酶体的功能机制提供了一些令人惊讶的见解,并将为该关键调节系统的遗传和生化研究提供宝贵的指导。