Arndt V, Rogon C, Höhfeld J
Institut für Zellbiologie, Rheinische Friedrich Wilhelms-Universität Bonn, Ulrich-Haberland-Str. 61a, 53121, Bonn, Germany.
Cell Mol Life Sci. 2007 Oct;64(19-20):2525-41. doi: 10.1007/s00018-007-7188-6.
To be, or not to be--that is the question not only for Hamlet in Shakespeare's drama but also for a protein associated with molecular chaperones. While long viewed exclusively as cellular folding factors, molecular chaperones recently emerged as active participants in protein degradation. This places chaperones at the center of a life or death decision during protein triage. Here we highlight molecular mechanisms that underlie chaperone action at the folding/degradation interface in mammalian cells. We discuss the importance of chaperone-assisted degradation for the regulation of cellular processes and its emerging role as a target for therapeutic intervention in cancer and amyloid diseases.
生存还是毁灭——这不仅是莎士比亚戏剧中哈姆雷特面临的问题,也是一种与分子伴侣相关的蛋白质所面临的问题。虽然分子伴侣长期以来一直被单纯视为细胞折叠因子,但最近它们成为了蛋白质降解过程中的积极参与者。这使得伴侣蛋白在蛋白质分类过程中的生死抉择中处于核心地位。在这里,我们重点介绍哺乳动物细胞中伴侣蛋白在折叠/降解界面发挥作用的分子机制。我们讨论了伴侣蛋白辅助降解对细胞过程调控的重要性,以及它作为癌症和淀粉样疾病治疗干预靶点的新作用。