Modulatory Effect of Nicotinamide Adenine Dinucleotide Phosphate (NADPH) on the 2-Oxoglutarate Mitochondrial Carrier

Author:

Spagnoletta Anna1ORCID,Miniero Daniela Valeria23ORCID,Gambacorta Nicola4ORCID,Oppedisano Francesca5ORCID,De Grassi Anna2ORCID,Nicolotti Orazio4ORCID,Pierri Ciro Leonardo4ORCID,De Palma Annalisa2ORCID

Affiliation:

1. Laboratory “Regenerative Circular Bioeconomy”, ENEA-Trisaia Research Centre, 75026 Rotondella, Italy

2. Department of Biosciences, Biotechnologies and Environment, University of Bari Aldo Moro, 70125 Bari, Italy

3. Department of Medicine & Surgery, LUM University Giuseppe Degennaro Torre Rossi, Piano 5 S.S. 100 Km. 18, 70010 Casamassima, Italy

4. Department of Pharmacy-Pharmaceutical Sciences, University of Bari Aldo Moro, 70125 Bari, Italy

5. Department of Health Sciences, Institute of Research for Food Safety and Health (IRC-FSH), University “Magna Graecia” of Catanzaro, 88100 Catanzaro, Italy

Abstract

The 2-oxoglutarate carrier (OGC), pivotal in cellular metabolism, facilitates the exchange of key metabolites between mitochondria and cytosol. This study explores the influence of NADPH on OGC transport activity using proteoliposomes. Experimental data revealed the ability of NADPH to modulate the OGC activity, with a significant increase of 60% at 0.010 mM. Kinetic analysis showed increased Vmax and a reduction in Km for 2-oxoglutarate, suggesting a direct regulatory role. Molecular docking pointed to a specific interaction between NADPH and cytosolic loops of OGC, involving key residues such as K206 and K122. This modulation was unique in mammalian OGC, as no similar effect was observed in a plant OGC structurally/functionally related mitochondrial carrier. These findings propose OGC as a responsive sensor for the mitochondrial redox state, coordinating with the malate/aspartate and isocitrate/oxoglutarate shuttles to maintain redox balance. The results underscore the potential role of OGC in redox homeostasis and its broader implications in cellular metabolism and oxidative stress responses.

Publisher

MDPI AG

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