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Choosing proper fluorescent dyes, proteins, and imaging techniques to study mitochondrial dynamics in mammalian cells
Author(s) -
Xingguo Liu,
Liang Yang,
Qi Long,
David T. Weaver,
György Hajnóczky
Publication year - 2017
Publication title -
biophysics reports
Language(s) - English
Resource type - Journals
eISSN - 2364-3420
pISSN - 2364-3439
DOI - 10.1007/s41048-017-0037-8
Subject(s) - mitophagy , microbiology and biotechnology , mitochondrial fusion , live cell imaging , mitochondrion , mitochondrial fission , green fluorescent protein , fluorescence lifetime imaging microscopy , biology , cell , mitochondrial biogenesis , biophysics , chemistry , fluorescence , mitochondrial dna , biochemistry , physics , gene , apoptosis , autophagy , quantum mechanics
Mitochondrial dynamics refers to the processes maintaining mitochondrial homeostasis, including mitochondrial fission, fusion, transport, biogenesis, and mitophagy. Mitochondrial dynamics is essential for maintaining the metabolic function of mitochondria as well as their regulatory roles in cell signaling. In this review, we summarize the recently developed imaging techniques for studying mitochondrial dynamics including: mitochondrial-targeted fluorescent proteins and dyes, live-cell imaging using photoactivation, photoswitching and cell fusion, mitochondrial transcription and replication imaging by in situ hybridization, and imaging mitochondrial dynamics by super-resolution microscopy. Moreover, we discuss examples of how to choose and combine proper fluorescent dyes and/or proteins.

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