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Role of GSH and Iron-Sulfur Glutaredoxins in Iron Metabolism-Review.


ABSTRACT: Glutathione (GSH) was initially identified and characterized for its redox properties and later for its contributions to detoxification reactions. Over the past decade, however, the essential contributions of glutathione to cellular iron metabolism have come more and more into focus. GSH is indispensable in mitochondrial iron-sulfur (FeS) cluster biosynthesis, primarily by co-ligating FeS clusters as a cofactor of the CGFS-type (class II) glutaredoxins (Grxs). GSH is required for the export of the yet to be defined FeS precursor from the mitochondria to the cytosol. In the cytosol, it is an essential cofactor, again of the multi-domain CGFS-type Grxs, master players in cellular iron and FeS trafficking. In this review, we summarize the recent advances and progress in this field. The most urgent open questions are discussed, such as the role of GSH in the export of FeS precursors from mitochondria, the physiological roles of the CGFS-type Grx interactions with BolA-like proteins and the cluster transfer between Grxs and recipient proteins.

SUBMITTER: Daniel T 

PROVIDER: S-EPMC7503856 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Role of GSH and Iron-Sulfur Glutaredoxins in Iron Metabolism-Review.

Daniel Trnka T   Faruq Hossain Md HM   Laura Magdalena Jordt J   Manuela Gellert G   Christopher Horst Lillig L  

Molecules (Basel, Switzerland) 20200825 17


Glutathione (GSH) was initially identified and characterized for its redox properties and later for its contributions to detoxification reactions. Over the past decade, however, the essential contributions of glutathione to cellular iron metabolism have come more and more into focus. GSH is indispensable in mitochondrial iron-sulfur (FeS) cluster biosynthesis, primarily by co-ligating FeS clusters as a cofactor of the CGFS-type (class II) glutaredoxins (Grxs). GSH is required for the export of t  ...[more]

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