4.7 Article

Optogenetic control of mitochondrial protonmotive force to impact cellular stress resistance

Journal

EMBO REPORTS
Volume 21, Issue 4, Pages -

Publisher

WILEY
DOI: 10.15252/embr.201949113

Keywords

anoxia; hypoxia; ischemia reperfusion; metabolism; uncoupling

Funding

  1. National Institutes of Health [R01 NS092558]
  2. University of Rochester
  3. American Heart Association Predoctoral Fellowship [18PRE33990054]
  4. Institutional Ruth L. Kirschstein National Research Service Award [NIH T32 GM068411]
  5. NSF [IOS1753742]
  6. NIH Office of Research Infrastructure Programs [P40 OD010440]

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Mitochondrial respiration generates an electrochemical proton gradient across the mitochondrial inner membrane called protonmotive force (PMF) to drive diverse functions and synthesize ATP. Current techniques to manipulate the PMF are limited to its dissipation; yet, there is no precise and reversible method to increase the PMF. To address this issue, we aimed to use an optogenetic approach and engineered a mitochondria-targeted light-activated proton pump that we name mitochondria-ON (mtON) to selectively increase the PMF in Caenorhabditis elegans. Here we show that mtON photoactivation increases the PMF in a dose-dependent manner, supports ATP synthesis, increases resistance to mitochondrial toxins, and modulates energy-sensing behavior. Moreover, transient mtON activation during hypoxic preconditioning prevents the well-characterized adaptive response of hypoxia resistance. Our results show that optogenetic manipulation of the PMF is a powerful tool to modulate metabolism and cell signaling.

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