Heme scavenging by plasma proteins, including serum albumin (SA), provides protection against free-heme oxidative damage, limits access by pathogens to the heme, and contributes to iron homeostasis by recycling the heme iron. In turn, serum heme-albumin (SA-heme) acquires heme-based ligand-binding and (pseudo-)enzymatic properties. Heme binding to SA and SA-heme reactivity are allosterically and competitively modulated by endogenous and exogenous third components, this being relevant in pharmacotherapy management.

Serum heme-albumin: an allosteric protein.

FASANO, MAURO
2009-01-01

Abstract

Heme scavenging by plasma proteins, including serum albumin (SA), provides protection against free-heme oxidative damage, limits access by pathogens to the heme, and contributes to iron homeostasis by recycling the heme iron. In turn, serum heme-albumin (SA-heme) acquires heme-based ligand-binding and (pseudo-)enzymatic properties. Heme binding to SA and SA-heme reactivity are allosterically and competitively modulated by endogenous and exogenous third components, this being relevant in pharmacotherapy management.
2009
http://dx.doi.org/10.1002/iub.263
Albumins, Allosteric Site, Binding Sites, Blood Proteins, Heme, Homeostasis, Humans, Kinetics, Ligands, Models; Molecular, Molecular Conformation, Oxidative Stress, Protein Binding, Serum Albumin
P., Ascenzi; Fasano, Mauro
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/1718490
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