蛋白质稳态
粒体自噬
生物
线粒体融合
细胞生物学
线粒体
蛋白酵素
DNAJA3公司
蛋白质毒性
MFN2型
胞浆
细胞器
自噬
线粒体DNA
蛋白质折叠
生物化学
酶
细胞凋亡
基因
作者
Michael J. Baker,Takashi Tatsuta,Thomas Langer
标识
DOI:10.1101/cshperspect.a007559
摘要
A decline in mitochondrial activity has been associated with aging and is a hallmark of many neurological diseases. Surveillance mechanisms acting at the molecular, organellar, and cellular level monitor mitochondrial integrity and ensure the maintenance of mitochondrial proteostasis. Here we will review the central role of mitochondrial chaperones and proteases, the cytosolic ubiquitin-proteasome system, and the mitochondrial unfolded response in this interconnected quality control network, highlighting the dual function of some proteases in protein quality control within the organelle and for the regulation of mitochondrial fusion and mitophagy.
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