Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, 610 Purdue Mall, West Lafayette, IN 47907, USA.
Molecules. 2019 Jun 25;24(12):2341. doi: 10.3390/molecules24122341.
Protein accumulation has been identified as a characteristic of many degenerative conditions, such as neurodegenerative diseases and aging. In most cases, these conditions also present with diminished protein degradation. The ubiquitin-proteasome system (UPS) is responsible for the degradation of the majority of proteins in cells; however, the activity of the proteasome is reduced in these disease states, contributing to the accumulation of toxic protein. It has been hypothesized that proteasome activity, both ubiquitin-dependent and -independent, can be chemically stimulated to reduce the load of protein in diseased cells. Several methods exist to identify and characterize stimulators of proteasome activity. In this review, we detail the ways in which protease activity can be enhanced and analyze the biochemical and cellular methods of identifying stimulators of both the ubiquitin-dependent and -independent proteasome activities.
蛋白质积累已被确定为许多退行性疾病的特征,如神经退行性疾病和衰老。在大多数情况下,这些疾病也存在蛋白质降解减少的情况。泛素-蛋白酶体系统(UPS)负责细胞中大多数蛋白质的降解;然而,在这些疾病状态下,蛋白酶体的活性降低,导致有毒蛋白质的积累。有人假设,蛋白酶体的活性,包括依赖和不依赖泛素的活性,可以通过化学刺激来减少病变细胞中的蛋白质负荷。有几种方法可以用来识别和描述蛋白酶体活性的刺激物。在这篇综述中,我们详细说明了如何增强蛋白酶活性,并分析了鉴定依赖和不依赖泛素的蛋白酶体活性刺激物的生化和细胞方法。