Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115.
Cold Spring Harb Perspect Biol. 2020 Jan 2;12(1):a033985. doi: 10.1101/cshperspect.a033985.
The proteasome, the most complex protease known, degrades proteins that have been conjugated to ubiquitin. It faces the unique challenge of acting enzymatically on hundreds and perhaps thousands of structurally diverse substrates, mechanically unfolding them from their native state and translocating them vectorially from one specialized compartment of the enzyme to another. Moreover, substrates are modified by ubiquitin in myriad configurations of chains. The many unusual design features of the proteasome may have evolved in part to endow this enzyme with a robust ability to process substrates regardless of their identity. The proteasome plays a major role in preserving protein homeostasis in the cell, which requires adaptation to a wide variety of stress conditions. Modulation of proteasome function is achieved through a large network of proteins that interact with it dynamically, modify it enzymatically, or fine-tune its levels. The resulting adaptability of the proteasome, which is unique among proteases, enables cells to control the output of the ubiquitin-proteasome pathway on a global scale.
蛋白酶体是已知的最复杂的蛋白酶,可降解与泛素缀合的蛋白质。它面临着一个独特的挑战,即要在数百种甚至数千种结构不同的底物上进行酶促反应,将它们从天然状态机械展开,并将它们从酶的一个特殊隔室向量转移到另一个隔室。此外,底物还可以通过泛素的多种链构型进行修饰。蛋白酶体的许多不寻常的设计特征可能是为了赋予该酶强大的处理底物的能力,而不论其身份如何。蛋白酶体在细胞中维持蛋白质内稳态方面发挥着重要作用,这需要适应各种应激条件。蛋白酶体功能的调节是通过与它动态相互作用、酶促修饰或精细调节其水平的大量蛋白质网络来实现的。蛋白酶体的这种适应性是其在蛋白酶中独一无二的,使细胞能够在全局范围内控制泛素-蛋白酶体途径的输出。