Monitoring Mitochondrial Protein Import Using Mitochondrial Targeting Sequence (MTS)-eGFP

被引:3
作者
Michaelis, Jonas B. [1 ]
Bozkurt, Sueleyman [1 ]
Schaefer, Jasmin A. [1 ]
Muench, Christian [1 ,2 ,3 ]
机构
[1] Goethe Univ Frankfurt, Inst Biochem 2, Fac Med, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[2] Frankfurt Canc Inst, Frankfurt, Germany
[3] Cardiopulm Inst, Frankfurt, Germany
来源
BIO-PROTOCOL | 2022年 / 12卷 / 24期
基金
欧洲研究理事会;
关键词
Mitochondrial protein import; Microscopy; Mitochondria; Protein translocation; Live cell imaging; PROTEOMICS;
D O I
10.21769/BioProtoc.4578
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mitochondria are cellular organelles essential for the function and survival of eukaryotic cells. Nearly all mitochondrial proteins are nuclear-encoded and require mitochondrial import upon their synthesis in the cytosol. Various approaches have been described to study mitochondrial protein import, such as monitoring the entry of radiolabeled proteins into purified mitochondria or quantifying newly synthesized proteins within mitochondria by proteomics. Here, we provide a detailed protocol for a commonly used and straightforward assay that quantitatively examines mitochondrial protein import by monitoring the co-localization of mitochondrially targeted enhanced green fluorescent protein (eGFP) with the mitochondrial fluorescence dye MitoTracker (TM) Deep Red FM by live cell imaging. We describe the preparation and use of a stable mammalian cell line inducibly expressing a mitochondrial targeting sequence (MTS)-eGFP, followed by quantitative image analysis using an open-source ImageJ-based plugin. This inducible expression system avoids the need for transient transfection while enabling titration of MTS-eGFP expression and thereby avoiding protein folding stress. Overall, the assay provides a simple and robust approach to assess mitochondrial import capacity of cells in various disease-related settings.
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页数:8
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