Super-resolution microscopy of mitochondria

被引:80
作者
Jakobs, Stefan [1 ,2 ]
Wurm, Christian A. [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37070 Gottingen, Germany
[2] Univ Gottingen, Sch Med, Dept Neurol, D-37073 Gottingen, Germany
关键词
PHOTOACTIVATED LOCALIZATION MICROSCOPY; STRUCTURED-ILLUMINATION MICROSCOPY; INNER MEMBRANE; FLUORESCENCE MICROSCOPY; STIMULATED-EMISSION; OXIDATIVE-PHOSPHORYLATION; ELECTRON-MICROSCOPY; 4PI MICROSCOPY; RESOLUTION; REVEALS;
D O I
10.1016/j.cbpa.2014.03.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria, the powerhouses of the cell, are essential organelles in eukaryotic cells. With their complex inner architecture featuring a smooth outer and a highly convoluted inner membrane, they are challenging objects for microscopy. The diameter of mitochondria is generally close to the resolution limit of conventional light microscopy, rendering diffraction-unlimited super-resolution light microscopy (nanoscopy) for imaging submitochondrial protein distributions often mandatory. In this review, we discuss what can be expected when imaging mitochondria with conventional diffraction-limited and diffraction-unlimited microscopy. We provide an overview on recent studies using super-resolution microscopy to investigate mitochondria and discuss further developments and challenges in mitochondrial biology that might by addressed with these technologies in the future.
引用
收藏
页码:9 / 15
页数:7
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