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Flavin-mediated reductive iron mobilization from frog M and Mycobacterial ferritins: impact of their size, charge and reactivities with NADH/O 2 .
- Source :
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Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry [J Biol Inorg Chem] 2021 May; Vol. 26 (2-3), pp. 265-281. Date of Electronic Publication: 2021 Feb 17. - Publication Year :
- 2021
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Abstract
- In vitro, reductive mobilization of ferritin iron using suitable electron transfer mediators has emerged as a possible mechanism to mimic the iron release process, in vivo. Nature uses flavins as electron relay molecules for important biological oxidation and oxygenation reactions. Therefore, the current work utilizes three flavin analogues: riboflavin (RF), flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), which differ in size and charge but have similar redox potentials, to relay electron from nicotinamide adenine dinucleotide (NADH) to ferritin mineral core. Of these, the smallest/neutral analogue, RF, released more iron (~ three fold) in comparison to the larger and negatively charged FMN and FAD. Although iron mobilization got marred during the initial stages under aerobic conditions, but increased with a greater slope at the later stages of the reaction kinetics, which gets inhibited by superoxide dismutase, consistent with the generation of O <subscript>2</subscript> <superscript>∙-</superscript> in situ. The initial step, i.e., interaction of flavins with NADH played critical role in the iron release process. Overall, the flavin-mediated reductive iron mobilization from ferritins occurred via two competitive pathways, involving the reduced form of flavins either alone (anaerobic condition) or in combination with O <subscript>2</subscript> <superscript>∙-</superscript> intermediate (aerobic condition). Moreover, faster iron release was observed for ferritins from Mycobacterium tuberculosis than from bullfrog, indicating the importance of protein nanocage and the advantages they provide to the respective organisms. Therefore, these structure-reactivity studies of flavins with NADH/O <subscript>2</subscript> holds significance in ferritin iron release, bioenergetics, O <subscript>2</subscript> -based cellular toxicity and may be potentially exploited in the treatment of methemoglobinemia. Smaller sized/neutral flavin analogue, riboflavin (RF) exhibits faster reactivity towards both NADH and O <subscript>2</subscript> generating more amount of O <subscript>2</subscript> <superscript>∙-</superscript> and releases higher amount of iron from different ferritins, compared to its larger sized/negatively charged derivatives such as FMN and FAD.
- Subjects :
- Animals
Oxygen metabolism
Oxygen chemistry
Flavin Mononucleotide chemistry
Flavin Mononucleotide metabolism
Riboflavin chemistry
Riboflavin metabolism
Riboflavin analogs & derivatives
NAD metabolism
NAD chemistry
Oxidation-Reduction
Iron metabolism
Iron chemistry
Flavins metabolism
Flavins chemistry
Ferritins chemistry
Ferritins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1432-1327
- Volume :
- 26
- Issue :
- 2-3
- Database :
- MEDLINE
- Journal :
- Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 33598740
- Full Text :
- https://doi.org/10.1007/s00775-021-01850-2