Tagging and tracking individual networks within a complex mitochondrial web with photoactivatable GFP

Gilad Twig, Solomon A. Graf, Jakob D. Wikstrom, Hibo Mohamed, Sarah E. Haigh, Alvaro Elorza, Motti Deutsch, Naomi Zurgil, Nicole Reynolds, Orian S. Shirihai

Research output: Contribution to journalArticlepeer-review

90 Citations (Scopus)

Abstract

Assembly of mitochondria into networks supports fuel metabolism and calcium transport and is involved in the cellular response to apoptotic stimuli. A mitochondrial network is defined as a continuous matrix lumen whose boundaries limit molecular diffusion. Observation of individual networks has proven challenging in live cells that possess dense populations of mitochondria. Investigation into the electrical and morphological properties of mitochondrial networks has therefore not yielded consistent conclusions. In this study we used matrix-targeted, photoactivatable green fluorescent protein to tag single mitochondrial networks. This approach, coupled with real-time monitoring of mitochondrial membrane potential, permitted the examination of matrix lumen continuity and fusion and fission events over time. We found that adjacent and intertwined mitochondrial structures often represent a collection of distinct networks. We additionally found that all areas of a single network are invariably equipotential, suggesting that a heterogeneous pattern of membrane potential within a cell's mitochondria represents differences between discrete networks. Interestingly, fission events frequently occurred without any gross morphological changes and particularly without fragmentation. These events, which are invisible under standard confocal microscopy, redefine the mitochondrial network boundaries and result in electrically disconnected daughter units.

Original languageEnglish
Pages (from-to)C176-C184
JournalAmerican Journal of Physiology - Cell Physiology
Volume291
Issue number1
DOIs
Publication statusPublished - 2006

Keywords

  • Fission
  • Fusion
  • Green fluorescent protein
  • Heterogeneity
  • Membrane potential
  • Tetramethylrhodamine ethyl ester perchlorate

ASJC Scopus subject areas

  • Physiology
  • Cell Biology

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