Goldberg Alfred L
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Nature. 2003 Dec 18;426(6968):895-9. doi: 10.1038/nature02263.
The ultimate mechanism that cells use to ensure the quality of intracellular proteins is the selective destruction of misfolded or damaged polypeptides. In eukaryotic cells, the large ATP-dependent proteolytic machine, the 26S proteasome, prevents the accumulation of non-functional, potentially toxic proteins. This process is of particular importance in protecting cells against harsh conditions (for example, heat shock or oxidative stress) and in a variety of diseases (for example, cystic fibrosis and the major neurodegenerative diseases). A full understanding of the pathogenesis of the protein-folding diseases will require greater knowledge of how misfolded proteins are recognized and selectively degraded.
细胞用于确保细胞内蛋白质质量的最终机制是对错误折叠或受损多肽进行选择性破坏。在真核细胞中,大型ATP依赖的蛋白水解机器——26S蛋白酶体,可防止无功能的、潜在有毒蛋白质的积累。这一过程在保护细胞免受恶劣条件(如热休克或氧化应激)影响以及在多种疾病(如囊性纤维化和主要的神经退行性疾病)中尤为重要。要全面了解蛋白质折叠疾病的发病机制,需要更深入地了解错误折叠的蛋白质是如何被识别和选择性降解的。