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Management versus miscues in the cytosolic labile iron pool: The varied functions of iron chaperones

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ELSEVIER
DOI: 10.1016/j.bbamcr.2020.118830

Keywords

Steatosis; Iron chaperone; PCBP; Ferroptosis; Glutathione

Funding

  1. intramural research program of National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, USA
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [ZIADK054510] Funding Source: NIH RePORTER

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Iron-containing proteins rely on the incorporation of a set of iron cofactors for activity. The cofactors must be synthesized or assembled from raw materials located within the cell. The chemical nature of this pool of raw material - referred to as the labile iron pool - has become clearer with the identification of micro- and macro-molecules that coordinate iron within the cell. These molecules function as a buffer system for the management of intracellular iron and are the focus of this review, with emphasis on the major iron chaperone protein coordinating the labile iron pool: poly C-binding protein 1.

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