Rivett A Jennifer, Bose Suchira, Pemberton Alexander J, Brooks Paul, Onion David, Shirley David, Stratford Fiona L L, Forti Katia
Department of Biochemistry, School of Medical Sciences, University of Bristol, Bristol BS8 1TD, UK.
Exp Gerontol. 2002 Oct-Nov;37(10-11):1217-22. doi: 10.1016/s0531-5565(02)00127-4.
Proteasomes play a major role in intracellular protein turnover. They exist in cells in several different molecular forms including 20S proteasomes, 26S proteasomes and PA28-20S proteasome complexes. In this study we have compared the properties of these purified proteasome complexes to try to design assays that will distinguish between the different complexes (26S proteasome, 20S proteasome, PA28-20S proteasome) in cell extracts. Although the different purified complexes were found to have differences in stability, and in their sensitivity to low concentrations of SDS and salt, the results suggest that it is not straightforward to assay selectively for each type of complex in cell extracts. The relative contribution of different proteasome complexes varies in different cell types and there may be other proteases present which hydrolyse the chosen substrate. Proteasome assays carried out under defined conditions allow comparisons of activity in cell extracts as a function of age, but separation by gel filtration on a Superose 6 column was found to be a useful method for determining the level of different proteasome related complexes.
蛋白酶体在细胞内蛋白质周转中起主要作用。它们以几种不同的分子形式存在于细胞中,包括20S蛋白酶体、26S蛋白酶体和PA28-20S蛋白酶体复合物。在本研究中,我们比较了这些纯化的蛋白酶体复合物的特性,试图设计出能够区分细胞提取物中不同复合物(26S蛋白酶体、20S蛋白酶体、PA28-20S蛋白酶体)的检测方法。尽管发现不同的纯化复合物在稳定性以及对低浓度十二烷基硫酸钠和盐的敏感性方面存在差异,但结果表明,在细胞提取物中选择性检测每种类型的复合物并非易事。不同蛋白酶体复合物的相对贡献在不同细胞类型中有所不同,并且可能存在其他水解所选底物的蛋白酶。在特定条件下进行的蛋白酶体检测可以比较细胞提取物中活性随年龄的变化情况,但发现在Superose 6柱上通过凝胶过滤进行分离是确定不同蛋白酶体相关复合物水平的一种有用方法。