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免疫印迹法评估自噬流。

Autophagic flux assessment by immunoblot.

机构信息

Department of Breast and Thyroid Surgery, Renmin Hospital of Wuhan University, Wuhan, Hubei, China; Centre de Recherche des Cordeliers, Équipe 11 Labellisée par la Ligue Contre le Cancer Université de Paris, Sorbonne Université, Inserm U1138, Institut Universitaire de France, Paris, France; Metabolomics and Cell Biology Platforms, Gustave Roussy Comprehensive Cancer Institute, Université Paris Saclay, Villejuif, France.

Centre de Recherche des Cordeliers, Équipe 11 Labellisée par la Ligue Contre le Cancer Université de Paris, Sorbonne Université, Inserm U1138, Institut Universitaire de France, Paris, France; Metabolomics and Cell Biology Platforms, Gustave Roussy Comprehensive Cancer Institute, Université Paris Saclay, Villejuif, France.

出版信息

Methods Cell Biol. 2021;164:63-72. doi: 10.1016/bs.mcb.2020.10.005. Epub 2021 Mar 1.

Abstract

Autophagy is one of the main adaptive mechanisms to maintain cellular homeostasis in response to multiple stresses. During autophagy diverse cellular components such as damaged organelles or superfluous proteins are targeted for lysosomal degradation. Importantly, during the initiation of autophagy MAP1LC3B (better known as LC3) lipidates into the membrane of the forming phagophore, which facilitates the formation and lengthening of autophagosomes. In addition, the autophagy receptor SQSTM1 (better known as p62) selectively recruits various cargos to autophagosomes for lysosomal degradation. Both, the conversion of LC3 as well as the degradation of p62 can be assessed as means of monitoring autophagy. Here we detail a protocol for assessing these key events of the autophagic flux via immunoblot.

摘要

自噬是细胞应对多种应激时维持细胞内环境稳定的主要适应机制之一。在自噬过程中,多种细胞成分,如受损的细胞器或多余的蛋白质,被靶向到溶酶体进行降解。重要的是,在自噬的起始阶段,MAP1LC3B(也称为 LC3)脂质化为正在形成的吞噬体的膜,这有助于自噬体的形成和延长。此外,自噬受体 SQSTM1(也称为 p62)选择性地将各种货物募集到自噬体进行溶酶体降解。LC3 的转化和 p62 的降解都可以作为监测自噬的手段。在这里,我们详细描述了通过免疫印迹评估自噬流中这些关键事件的方案。

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