From the Department of Developmental and Molecular Biology, Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, New York 10461.
From the Department of Developmental and Molecular Biology, Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, New York 10461
J Biol Chem. 2018 Apr 13;293(15):5414-5424. doi: 10.1074/jbc.R117.818237. Epub 2017 Dec 15.
A variety of mechanisms deliver cytosolic materials to the lysosomal compartment for degradation through autophagy. Here, we focus on two autophagic pathways, the chaperone-mediated autophagy and the endosomal microautophagy that rely on the cytosolic chaperone hsc70 for substrate targeting. Although hsc70 participates in the triage of proteins for degradation by different proteolytic systems, the common characteristic shared by these two forms of autophagy is that hsc70 binds directly to a specific five-amino acid motif in the cargo protein for its autophagic targeting. We summarize the current understanding of the molecular machineries behind each of these types of autophagy.
多种机制将细胞质物质递送至溶酶体隔室进行降解,通过自噬。在这里,我们重点关注两种自噬途径,即伴侣介导的自噬和内体微自噬,它们依赖于细胞质伴侣 hsc70 进行底物靶向。虽然 hsc70 参与了不同蛋白水解系统对蛋白质降解的分类,但这两种形式的自噬的共同特征是 hsc70 直接结合到货物蛋白中的特定五氨基酸基序,以进行自噬靶向。我们总结了目前对这两种自噬类型背后的分子机制的理解。