利用体外重组系统可视化细胞自噬溶酶体重组

Q3 Biochemistry, Genetics and Molecular Biology Current Protocols in Cell Biology Pub Date : 2018-04-09 DOI:10.1002/cpcb.44
Yang Chen, Qian Peter Su, Yujie Sun, Li Yu
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引用次数: 6

摘要

自噬是一种基于溶酶体的降解途径。自噬溶酶体重组(Autophagic lysosome重整,ALR)是溶酶体膜循环过程,标志着自噬的最后一步。在ALR过程中,从自溶酶体中挤出lamp1阳性小管,称为重组小管,新生溶酶体从这些小管中产生。通过对纯化的自溶酶体进行蛋白质组学分析,并对鉴定出的候选物进行RNA干扰筛选,我们在分子水平上系统地阐明了ALR途径。基于关键成分网格蛋白、PtdIns(4,5)P2和马达蛋白KIF5B等,我们在体外重建了这一过程。本单元详细介绍了自噬过程中细胞内ALR的可视化方法。本单元还提出了体外重建ALR管状突起和伸长过程的方案,以及制备体外重建材料的三种方法:(1)从培养细胞中纯化自溶酶体,(2)脂质体制备,(3)KIF5B纯化和质量检测。©2018 by John Wiley &儿子,Inc。
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Visualizing Autophagic Lysosome Reformation in Cells Using In Vitro Reconstitution Systems

Autophagy is a lysosome-based degradation pathway. Autophagic lysosome reformation (ALR) is a lysosomal membrane recycling process that marks the terminal step of autophagy. During ALR, LAMP1-positive tubules, named reformation tubules, are extruded from autolysosomes, and nascent lysosomes are generated from these tubules. By combining proteomic analysis of purified autolysosomes and RNA interference screening of identified candidates, we systematically elucidated the ALR pathway at the molecular level. Based on the key components clathrin, PtdIns(4,5)P2, and the motor protein KIF5B, among others, we reconstituted this process in vitro. This unit describes a detailed method for visualizing ALR in cells during the autophagy process. This unit also present a protocol for reconstituting the ALR tubular protrusion and elongation process in vitro and three methods for preparing materials for in vitro reconstitution: (1) autolysosome purification from cultured cells, (2) liposome preparation, and (3) KIF5B purification and quality testing. © 2018 by John Wiley & Sons, Inc.

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Current Protocols in Cell Biology
Current Protocols in Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
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期刊介绍: Developed by leading scientists in the field, Current Protocols in Cell Biology is an essential reference for researchers who study the relationship between specific molecules and genes and their location, function and structure at the cellular level. Updated every three months in all formats, CPCB is constantly evolving to keep pace with the very latest discoveries and developments.
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