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A family of NADPH/NADP biosensors reveals in vivo dynamics of central redox metabolism across eukaryotes. | LitMetric

AI Article Synopsis

  • The NADPH/NADP redox couple plays a crucial role in metabolism and redox signaling, but understanding its dynamics at the subcellular level has been challenging due to limited tools.
  • The study introduces NAPstars, a new family of genetically encoded fluorescent protein-based biosensors that allow for real-time and specific measurements of NADP redox states with subcellular resolution.
  • NAPstars reveal consistent patterns of NADP redox stability in various cell types, highlight cell cycle-related redox fluctuations in yeast, and show how changes in illumination and oxygen levels affect redox states in plant leaves, emphasizing the importance of the glutathione system in managing oxidative stress.

Article Abstract

The NADPH/NADP redox couple is central to metabolism and redox signalling. NADP redox state is differentially regulated by distinct enzymatic machineries at the subcellular compartment level. Nonetheless, a detailed understanding of subcellular NADP redox dynamics is limited by the availability of appropriate tools. Here, we introduce NAPstars, a family of genetically encoded, fluorescent protein-based NADP redox state biosensors. NAPstars offer real-time, specific measurements, across a broad-range of NADP redox states, with subcellular resolution. NAPstar measurements in yeast, plants, and mammalian cell models, reveal a conserved robustness of cytosolic NADP redox homoeostasis. NAPstars uncover cell cycle-linked NADP redox oscillations in yeast and illumination- and hypoxia-dependent NADP redox changes in plant leaves. By applying NAPstars in combination with selective impairment of the glutathione and thioredoxin antioxidative pathways under acute oxidative challenge, we find an unexpected and conserved role for the glutathione system as the primary mediator of antioxidative electron flux.

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Source
http://dx.doi.org/10.1038/s41467-024-55302-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11659435PMC

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