4.6 Article

Approaches to monitor ATP levels in living cells: where do we stand?

Journal

FEBS JOURNAL
Volume 289, Issue 24, Pages 7940-7969

Publisher

WILEY
DOI: 10.1111/febs.16169

Keywords

ATP; ATP synthase; biochemical assays; fluorescence-based tools; mitochondria

Funding

  1. Centre National de la Recherche Scientifique (CNRS)
  2. Association Nationale Recherche Technologie (ANRT)
  3. LVMH RESEARCH

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ATP, as the most universal and essential energy molecule in cells, plays a crucial role in various biological functions. Understanding its production and hydrolysis processes is necessary for comprehending its physiological and pathological functions. This review discusses the organization of electron transport chain and ATP synthase, methods for estimating ATP quantities in cells, and genetically encoded biosensors for monitoring ATP levels in living cells.
ATP is the most universal and essential energy molecule in cells. This is due to its ability to store cellular energy in form of high-energy phosphate bonds, which are extremely stable and readily usable by the cell. This energy is key for a variety of biological functions such as cell growth and division, metabolism, and signaling, and for the turnover of biomolecules. Understanding how ATP is produced and hydrolyzed with a spatiotemporal resolution is necessary to understand its functions both in physiological and in pathological contexts. In this review, first we will describe the organization of the electron transport chain and ATP synthase, the main molecular motor for ATP production in mitochondria. Second, we will review the biochemical assays currently available to estimate ATP quantities in cells, and we will compare their readouts, strengths, and weaknesses. Finally, we will explore the palette of genetically encoded biosensors designed for microscopy-based approaches, and show how their spatiotemporal resolution opened up the possibility to follow ATP levels in living cells.

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