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体外研究Atg8介导的膜动力学的方法。

Approaches to the study of Atg8-mediated membrane dynamics in vitro.

作者信息

Jotwani Anjali, Richerson Diana N, Motta Isabelle, Julca-Zevallos Omar, Melia Thomas J

机构信息

Department of Cell Biology, Yale School of Medicine, Connecticut, USA.

出版信息

Methods Cell Biol. 2012;108:93-116. doi: 10.1016/B978-0-12-386487-1.00005-5.

Abstract

Macro-autophagy is the intracellular stress-response pathway by which the cell packages portions of the cytosol for delivery into the lysosome. This "packaging" is carried out by the de novo formation of a new organelle called the autophagosome that grows and encapsulates cytosolic material for eventual lysosomal degradation. How autophagosomes form, including especially how the membrane expands and eventually closes upon itself is an area of intense study. One factor implicated in both membrane expansion and membrane fusion is the ubiquitin-like protein, Atg8. During autophagy, Atg8 becomes covalently bound to phosphatidylethanolamine (PE) on the pre-autophagosomal membrane and remains bound through the maturation process of the autophagosome. In this chapter, we discuss two approaches to the in vitro reconstitution of this lipidation reaction. We then describe methods to study Atg8-PE mediated membrane tethering and fusion, two functions implicated in Atg8's role in autophagosome maturation.

摘要

巨自噬是一种细胞内应激反应途径,通过该途径细胞将部分胞质溶胶包裹起来,以便输送到溶酶体中。这种“包裹”是通过一种新形成的称为自噬体的细胞器来完成的,自噬体生长并包裹胞质物质,最终进行溶酶体降解。自噬体如何形成,尤其是膜如何扩张并最终自身闭合,是一个深入研究的领域。一种与膜扩张和膜融合都有关的因素是泛素样蛋白Atg8。在自噬过程中,Atg8共价结合到自噬体前体膜上的磷脂酰乙醇胺(PE)上,并在自噬体的成熟过程中一直保持结合状态。在本章中,我们讨论了两种体外重建这种脂化反应的方法。然后我们描述了研究Atg8-PE介导的膜拴系和融合的方法,这是Atg8在自噬体成熟过程中涉及的两种功能。

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