Regulations of mitoNEET by the key redox homeostasis molecule glutathione - DSA-IPHC
Journal Articles Journal of Inorganic Biochemistry Year : 2024

Regulations of mitoNEET by the key redox homeostasis molecule glutathione

Abstract

Human mitoNEET (mNT) and CISD2 are two NEET proteins characterized by an atypical [2Fe-2S] cluster coordination involving three cysteines and one histidine. They act as redox switches with an active state linked to the oxidation of their cluster. In the present study, we show that reduced glutathione but also free thiol-containing molecules such as β-mercaptoethanol can induce a loss of the mNT cluster under aerobic conditions, while CISD2 cluster appears more resistant. This disassembly occurs through a radical-based mechanism as previously observed with the bacterial SoxR. Interestingly, adding cysteine prevents glutathione-induced cluster loss. At low pH, glutathione can bind mNT in the vicinity of the cluster. These results suggest a potential new regulation mechanism of mNT activity by glutathione, an essential actor of the intracellular redox state.
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hal-04520876 , version 1 (25-03-2024)

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Cécile Mons, Myriam Salameh, Thomas Botzanowski, Martin Clémancey, Pierre Dorlet, et al.. Regulations of mitoNEET by the key redox homeostasis molecule glutathione. Journal of Inorganic Biochemistry, 2024, 255, ⟨10.1016/j.jinorgbio.2024.112535⟩. ⟨hal-04520876⟩
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