The NAPstar family of NADP redox state sensors highlights glutathione as the primary mediator of anti-oxidative electron flux
Marie ScherscheliD, Jan-Ole NiemeieriD, Lianne H.C. JacobsiD, Markus D. A. HoffmanniD, Anika DiederichiD, Christopher BelliD, Pascal HöhneiD, Sonja RaetziD, Johanna B. KrolliD, Janina SteinbeckiD, Sophie LichtenaueriD, Jan MulthoffiD, Jannik ZimmermanniD, Tanmay SadhanasatishiD, Robin Alexander RothemanniD, Carsten GrashoffiD, Joris MessensiD, Emmanuel AmpofoiD, Matthias W. LaschkeiD, Jan RiemeriD, Letícia Prates RomaiD, Markus SchwarzländeriD, Bruce MorganiD
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, pH-resistant measurements, across a broad-range of NADP redox states, with subcellular resolution. We establish NAPstar measurements in yeast, plants and mammalian cell models, revealing a conserved robustness of cytosolic NADP redox homeostasis. NAPstars uncovered NADP redox oscillations linked to the cell cycle in yeast and illumination- and hypoxia-dependent NADP redox changes in plant leaves. By selectively impairing the glutathione and thioredoxin anti-oxidative pathways under acute oxidative challenge, NAPstars demonstrated an unexpected role for the glutathione system as the primary mediator of anti-oxidative electron flux that is conserved across eukaryotic kingdoms.
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