Institute of Molecular Biology (IMB), Mainz, Germany.
Department of Chemistry and Institute for Advanced Study, Technical University of Munich, Garching, Germany.
Exp Cell Res. 2021 Jun 15;403(2):112617. doi: 10.1016/j.yexcr.2021.112617. Epub 2021 Apr 28.
A healthy and functional proteome is essential to cell physiology. However, this is constantly being challenged as most steps of protein metabolism are error-prone and changes in the physico-chemical environment can affect protein structure and function, thereby disrupting proteome homeostasis. Among a variety of potential mistakes, proteins can be targeted to incorrect compartments or subunits of protein complexes may fail to assemble properly with their partners, resulting in the formation of mislocalized and orphan proteins, respectively. Quality control systems are in place to handle these aberrant proteins, and to minimize their detrimental impact on cellular functions. Here, we discuss recent findings on quality control mechanisms handling mislocalized and orphan proteins. We highlight common principles involved in their recognition and summarize how accumulation of these aberrant molecules is associated with aging and disease.
健康且功能正常的蛋白质组对于细胞生理学至关重要。然而,由于蛋白质代谢的大多数步骤都容易出错,并且理化环境的变化会影响蛋白质的结构和功能,从而破坏蛋白质组的平衡,这种理想状态不断受到挑战。在各种潜在的错误中,蛋白质可能会被靶向到错误的隔室,或者蛋白质复合物的亚基可能无法与其伴侣正确组装,从而分别形成定位错误的蛋白质和孤儿蛋白质。有质量控制系统来处理这些异常蛋白质,并将它们对细胞功能的有害影响降到最低。在这里,我们讨论了最近关于处理定位错误的蛋白质和孤儿蛋白质的质量控制机制的发现。我们强调了它们识别过程中的共同原则,并总结了这些异常分子的积累如何与衰老和疾病有关。