Maruyama Tatsuro, Noda Nobuo N
Laboratory of Structural Biology, Institute of Microbial Chemistry, Tokyo, Japan.
J Antibiot (Tokyo). 2017 Sep 13;71(1):72-8. doi: 10.1038/ja.2017.104.
Autophagy is an intracellular degradation system that contributes to cellular homeostasis through degradation of various targets such as proteins, organelles and microbes. Since autophagy is related to various diseases such as infection, neurodegenerative diseases and cancer, it is attracting attention as a new therapeutic target. Autophagy is mediated by dozens of autophagy-related (Atg) proteins, among which Atg4 is the sole protease that regulates autophagy through the processing and deconjugating of Atg8. As the Atg4 activity is essential and highly specific to autophagy, Atg4 is a prospective target for developing autophagy-specific inhibitors. In this review article, we summarize our current knowledge of the structure, function and regulation of Atg4 including efforts to develop Atg4-specific inhibitors.The Journal of Antibiotics advance online publication, 13 September 2017; doi:10.1038/ja.2017.104.
自噬是一种细胞内降解系统,通过降解蛋白质、细胞器和微生物等各种靶标来维持细胞内稳态。由于自噬与感染、神经退行性疾病和癌症等多种疾病相关,它作为一个新的治疗靶点正受到关注。自噬由数十种自噬相关(Atg)蛋白介导,其中Atg4是唯一通过对Atg8进行加工和解偶联来调节自噬的蛋白酶。由于Atg4活性对自噬至关重要且具有高度特异性,Atg4是开发自噬特异性抑制剂的一个潜在靶点。在这篇综述文章中,我们总结了目前关于Atg4的结构、功能和调控的知识,包括开发Atg4特异性抑制剂的相关研究。《抗生素杂志》2017年9月13日在线优先发表;doi:10.1038/ja.2017.104 。