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监测线粒体翻译的方法。

Assays to monitor mitochondrial translation.

机构信息

Department of Medical Biochemistry and Cell biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Department of Medical Biochemistry and Cell biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

Methods Enzymol. 2024;706:519-532. doi: 10.1016/bs.mie.2024.07.045. Epub 2024 Aug 13.

Abstract

The complexes of the oxidative phosphorylation (OXPHOS) system found in the mitochondrial inner membrane comprises nuclear and mitochondrial-encoded proteins. The mitochondrial-encoded subunits of the OXPHOS complexes play vital catalytic roles for OXPHOS. These subunits are inserted co-translationally into the inner membrane, where they are matured and assembled with nuclear encoded subunits, requiring a set of OXPHOS assembly and quality control factors. Hence, monitoring the fate of newly synthesized mitochondrial-encoded polypeptides is a basic and essential approach for exploring OXPHOS biogenesis and the related protein quality control processes. Here, we describe a detailed protocol for labeling mitochondrial encoded proteins with S-methionine for pulse and pulse/chase experiments, both in vivo and in organello, using the yeast Saccharomyces cerevisiae as the model. These methods enable analyses of the early steps during the biogenesis and turnover of mitochondrial-encoded proteins.

摘要

在线粒体膜内发现的氧化磷酸化(OXPHOS)系统的复合物包含核编码和线粒体编码的蛋白质。OXPHOS 复合物的线粒体编码亚基对于 OXPHOS 起着至关重要的催化作用。这些亚基在共翻译过程中被插入到内膜中,在那里它们与核编码亚基成熟和组装,需要一组 OXPHOS 组装和质量控制因子。因此,监测新合成的线粒体编码多肽的命运是探索 OXPHOS 生物发生和相关蛋白质质量控制过程的基本和必要方法。在这里,我们描述了一种使用酿酒酵母作为模型的详细方案,用于脉冲和脉冲/追踪实验中用 S-甲硫氨酸标记线粒体编码蛋白,无论是在体内还是在器官水平上。这些方法能够分析线粒体编码蛋白生物发生和周转的早期步骤。

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