Literature DB >> 33598740

Flavin-mediated reductive iron mobilization from frog M and Mycobacterial ferritins: impact of their size, charge and reactivities with NADH/O2.

Prashanth Kumar Koochana1, Abhinav Mohanty1, Akankshika Parida1, Narmada Behera1, Pabitra Mohan Behera2, Anshuman Dixit2, Rabindra K Behera3.   

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 O2∙- 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 O2∙- 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/O2 holds significance in ferritin iron release, bioenergetics, O2-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 O2 generating more amount of O2∙- and releases higher amount of iron from different ferritins, compared to its larger sized/negatively charged derivatives such as FMN and FAD.

Entities:  

Keywords:  Bacterioferritin; Electron transfer; Ferritin; Flavins; Iron release; Mediator

Year:  2021        PMID: 33598740     DOI: 10.1007/s00775-021-01850-2

Source DB:  PubMed          Journal:  J Biol Inorg Chem        ISSN: 0949-8257            Impact factor:   3.358


  55 in total

Review 1.  Unity in the biochemistry of the iron-storage proteins ferritin and bacterioferritin.

Authors:  Kourosh Honarmand Ebrahimi; Peter-Leon Hagedoorn; Wilfred R Hagen
Journal:  Chem Rev       Date:  2014-11-24       Impact factor: 60.622

Review 2.  Use of the confined spaces of apo-ferritin and virus capsids as nanoreactors for catalytic reactions.

Authors:  Basudev Maity; Kenta Fujita; Takafumi Ueno
Journal:  Curr Opin Chem Biol       Date:  2015-01-08       Impact factor: 8.822

3.  Iron Mineralizing Bacterioferritin A from Mycobacterium tuberculosis Exhibits Unique Catalase-Dps-like Dual Activities.

Authors:  Abhinav Mohanty; Biswamaitree Subhadarshanee; Pallavi Barman; Chinmayee Mahapatra; B Aishwarya; Rabindra K Behera
Journal:  Inorg Chem       Date:  2019-03-28       Impact factor: 5.165

4.  Moving Fe2+ from ferritin ion channels to catalytic OH centers depends on conserved protein cage carboxylates.

Authors:  Rabindra K Behera; Elizabeth C Theil
Journal:  Proc Natl Acad Sci U S A       Date:  2014-05-19       Impact factor: 11.205

Review 5.  The iron redox and hydrolysis chemistry of the ferritins.

Authors:  Fadi Bou-Abdallah
Journal:  Biochim Biophys Acta       Date:  2010-04-09

6.  Moving metal ions through ferritin-protein nanocages from three-fold pores to catalytic sites.

Authors:  Takehiko Tosha; Ho-Leung Ng; Onita Bhattasali; Tom Alber; Elizabeth C Theil
Journal:  J Am Chem Soc       Date:  2010-10-20       Impact factor: 15.419

7.  Fe(2+) substrate transport through ferritin protein cage ion channels influences enzyme activity and biomineralization.

Authors:  Rabindra K Behera; Rodrigo Torres; Takehiko Tosha; Justin M Bradley; Celia W Goulding; Elizabeth C Theil
Journal:  J Biol Inorg Chem       Date:  2015-07-23       Impact factor: 3.358

8.  Solving Biology's Iron Chemistry Problem with Ferritin Protein Nanocages.

Authors:  Elizabeth C Theil; Takehiko Tosha; Rabindra K Behera
Journal:  Acc Chem Res       Date:  2016-05-02       Impact factor: 22.384

9.  Ferritins for Chemistry and for Life.

Authors:  Elizabeth C Theil; Rabindra K Behera; Takehiko Tosha
Journal:  Coord Chem Rev       Date:  2012-05-18       Impact factor: 22.315

10.  Impact of Phosphate on Iron Mineralization and Mobilization in Nonheme Bacterioferritin B from Mycobacterium tuberculosis.

Authors:  Akankshika Parida; Abhinav Mohanty; Bharat T Kansara; Rabindra K Behera
Journal:  Inorg Chem       Date:  2019-12-10       Impact factor: 5.165

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  1 in total

1.  Iron Mobilization from Ferritin in Yeast Cell Lysate and Physiological Implications.

Authors:  Gideon L Smith; Ayush K Srivastava; Aliaksandra A Reutovich; Nathan J Hunter; Paolo Arosio; Artem Melman; Fadi Bou-Abdallah
Journal:  Int J Mol Sci       Date:  2022-05-29       Impact factor: 6.208

  1 in total

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