Department of Biology, Stanford University, Stanford, California 94305; email:
Annu Rev Biochem. 2017 Jun 20;86:97-122. doi: 10.1146/annurev-biochem-060815-014616. Epub 2017 May 10.
A healthy proteome is essential for cell survival. Protein misfolding is linked to a rapidly expanding list of human diseases, ranging from neurodegenerative diseases to aging and cancer. Many of these diseases are characterized by the accumulation of misfolded proteins in intra- and extracellular inclusions, such as amyloid plaques. The clear link between protein misfolding and disease highlights the need to better understand the elaborate machinery that manages proteome homeostasis, or proteostasis, in the cell. Proteostasis depends on a network of molecular chaperones and clearance pathways involved in the recognition, refolding, and/or clearance of aberrant proteins. Recent studies reveal that an integral part of the cellular management of misfolded proteins is their spatial sequestration into several defined compartments. Here, we review the properties, function, and formation of these compartments. Spatial sequestration plays a central role in protein quality control and cellular fitness and represents a critical link to the pathogenesis of protein aggregation-linked diseases.
健康的蛋白质组对于细胞存活至关重要。蛋白质错误折叠与一系列人类疾病相关联,范围从神经退行性疾病到衰老和癌症。这些疾病中的许多疾病的特征是错误折叠的蛋白质在细胞内和细胞外包含物(如淀粉样斑块)中的积累。蛋白质错误折叠与疾病之间的明确联系突出表明需要更好地理解管理细胞中蛋白质组平衡或蛋白质稳态的精细机制。蛋白质稳态依赖于参与识别、重折叠和/或清除异常蛋白质的分子伴侣和清除途径的网络。最近的研究揭示了细胞内错误折叠蛋白质的一个重要管理部分是将它们空间隔离到几个定义明确的隔室中。在这里,我们综述了这些隔室的特性、功能和形成。空间隔离在蛋白质质量控制和细胞适应性中起着核心作用,并且是与蛋白质聚集相关疾病发病机制的关键联系。