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Ceruloplasmin is a serum ferroxidase that contains greater than 95% of the copper found in plasma. This protein is a member of the multicopper oxidase family, an evolutionarily conserved group of proteins that utilize copper to couple substrate oxidation with the four-electron reduction of oxygen to water. Despite the need for copper in ceruloplasmin function, this protein plays no essential role in the transport or metabolism of this metal. Aceruloplasminemia is a neurodegenerative disease resulting from inherited loss-of-function mutations in the ceruloplasmin gene. Characterization of this disorder revealed a critical physiological role for ceruloplasmin in determining the rate of iron efflux from cells with mobilizable iron stores and has provided new insights into human iron metabolism and nutrition.
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Nathan E. Hellman
Délégation Paris 5
Jonathan D. Gitlin
University of Vermont
Annual Review of Nutrition
Mallinckrodt (United States)
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Hellman et al. (Mon,) studied this question.
synapsesocial.com/papers/6a013abab124fe5819864b16 — DOI: https://doi.org/10.1146/annurev.nutr.22.012502.114457
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