Institute of Microbial Chemistry (Bikaken), Tokyo 141-0021, Japan.
Biochem Soc Trans. 2020 Oct 30;48(5):2003-2014. doi: 10.1042/BST20200130.
Autophagy is a lysosomal degradation system that involves de novo autophagosome formation. A lot of factors are involved in autophagosome formation, including dozens of Atg proteins that form supramolecular complexes, membrane structures including vesicles and organelles, and even membraneless organelles. Because these diverse higher-order structural components cooperate to mediate de novo formation of autophagosomes, it is too complicated to be elaborated only by cell biological approaches. Recent trials to regenerate each step of this phenomenon in vitro have started to elaborate on the molecular mechanisms of such a complicated process by simplification. In this review article, we outline the in vitro reconstitution trials in autophagosome formation, mainly focusing on the reports in the past few years and discussing the molecular mechanisms of autophagosome formation by comparing in vitro and in vivo observations.
自噬是一种溶酶体降解系统,涉及新的自噬体形成。自噬体形成涉及许多因素,包括数十种形成超分子复合物的 Atg 蛋白、包括囊泡和细胞器在内的膜结构,甚至无膜细胞器。由于这些不同的高级结构成分合作介导新的自噬体形成,因此仅通过细胞生物学方法来详细阐述是非常复杂的。最近尝试在体外重新生成这一现象的每一步骤,已经通过简化开始详细阐述这一复杂过程的分子机制。在这篇综述文章中,我们概述了自噬体形成的体外重建试验,主要集中在过去几年的报告,并通过比较体外和体内观察来讨论自噬体形成的分子机制。