Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, Am Klopferspitz 18, D-82152 Martinsried, Germany.
Biol Chem. 2019 Dec 18;401(1):183-199. doi: 10.1515/hsz-2019-0344.
Proteasomes are the principal molecular machines for the regulated degradation of intracellular proteins. These self-compartmentalized macromolecular assemblies selectively degrade misfolded, mistranslated, damaged or otherwise unwanted proteins, and play a pivotal role in the maintenance of cellular proteostasis, in stress response, and numerous other processes of vital importance. Whereas the molecular architecture of the proteasome core particle (CP) is universally conserved, the unfoldase modules vary in overall structure, subunit complexity, and regulatory principles. Proteasomal unfoldases are AAA+ ATPases (ATPases associated with a variety of cellular activities) that unfold protein substrates, and translocate them into the CP for degradation. In this review, we summarize the current state of knowledge about proteasome - unfoldase systems in bacteria, archaea, and eukaryotes, the three domains of life.
蛋白酶体是调节细胞内蛋白质降解的主要分子机器。这些自我分隔的大分子组装体选择性地降解错误折叠、翻译错误、受损或其他不需要的蛋白质,并在维持细胞蛋白平衡、应激反应和许多其他至关重要的过程中发挥关键作用。虽然蛋白酶体核心颗粒(CP)的分子结构普遍保守,但解折叠酶模块在整体结构、亚基复杂性和调节原则上有所不同。蛋白酶体解折叠酶是 AAA+ATP 酶(与多种细胞活动相关的 ATP 酶),可展开蛋白质底物,并将其转运到 CP 中进行降解。在这篇综述中,我们总结了生命的三个领域,即细菌、古菌和真核生物中蛋白酶体-解折叠酶系统的最新知识状态。