McShane Erik, Selbach Matthias
Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA; email:
Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany; email:
Annu Rev Cell Dev Biol. 2022 Oct 6;38:241-262. doi: 10.1146/annurev-cellbio-120420-091943. Epub 2022 May 19.
While cellular proteins were initially thought to be stable, research over the last decades has firmly established that intracellular protein degradation is an active and highly regulated process: Lysosomal, proteasomal, and mitochondrial degradation systems were identified and found to be involved in a staggering number of biological functions. Here, we provide a global overview of the diverse roles of cellular protein degradation using seven categories: homeostasis, regulation, quality control, stoichiometry control, proteome remodeling, immune surveillance, and baseline turnover. Using selected examples, we outline how proteins are degraded and why this is functionally relevant.
虽然细胞蛋白最初被认为是稳定的,但过去几十年的研究已经确凿地证实,细胞内蛋白质降解是一个活跃且高度受调控的过程:溶酶体、蛋白酶体和线粒体降解系统已被识别,并发现它们参与了数量惊人的生物学功能。在此,我们从七个类别对细胞蛋白质降解的多种作用进行全面概述:稳态、调节、质量控制、化学计量控制、蛋白质组重塑、免疫监视和基础更新。通过选取的实例,我们概述了蛋白质是如何被降解的以及其功能相关性的原因。