Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states

All fish hemoglobins (Hb) show a high auto-oxidation rate, and some fish Hbs are endowed with Root effect (drastic drop of cooperativity at acidic pH). Differently from temperate fish Hbs, at physiological pH Antarctic fish Hbs (AFHbs) in the ferric state show both an aquomet form and two distinct h...

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Main Authors: VERGARA, ALESSANDRO, MERLINO, ANTONELLO, L. Vitagliano, G. Barbiero, C. Verde, G. di Prisco, Lelio Mazzarella
Other Authors: Vergara, Alessandro, L., Vitagliano, G., Barbiero, Merlino, Antonello, C., Verde, G., di Prisco, Lelio, Mazzarella
Format: Conference Object
Language:English
Published: country:DNK 2008
Subjects:
Online Access:http://hdl.handle.net/11588/346251
http://www.o2bip2008.dk/index.html
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author VERGARA, ALESSANDRO
MERLINO, ANTONELLO
L. Vitagliano
G. Barbiero
C. Verde
G. di Prisco
Lelio Mazzarella
author2 Vergara, Alessandro
L., Vitagliano
G., Barbiero
Merlino, Antonello
C., Verde
G., di Prisco
Lelio, Mazzarella
author_facet VERGARA, ALESSANDRO
MERLINO, ANTONELLO
L. Vitagliano
G. Barbiero
C. Verde
G. di Prisco
Lelio Mazzarella
author_sort VERGARA, ALESSANDRO
collection IRIS Università degli Studi di Napoli Federico II
description All fish hemoglobins (Hb) show a high auto-oxidation rate, and some fish Hbs are endowed with Root effect (drastic drop of cooperativity at acidic pH). Differently from temperate fish Hbs, at physiological pH Antarctic fish Hbs (AFHbs) in the ferric state show both an aquomet form and two distinct hemichromes within a R / T intermediate quaternary structure (1). Interestingly, AFHbs exhibit a peroxidase activity higher than that observed for mammalian and temperate fish Hbs, thus suggesting that a partial hemichrome state in tetrameric Hbs does not protect them from peroxidation as previously proposed (2). At acidic pH, a combined EPR / x-ray crystallography approach has revealed, only for Root-effect AFHbs, significant amount of pentacoordinated (5C) high-spin Fe(III) species.(3) Furthermore, along the oxidation pathway, a combined x-ray crystallography / Resonance Raman spectroscopy of AFHbs has revealed a hybrid valence state [α(O2)/β(Fe3+, pentacoordinate)].(4) This valence hybrid states prompted us to test a FeSOD activity, that is as low as human Hb. A combined x-ray crystallography / FT-IR study has revealed at least two coordination states of the carbomonoxy form of AFHbs, one corresponding to a His assisted CO binding (band III at 1951 cm-1), and another to a not-His assisted CO binding (band IV at 1968 cm-1). The band IV, typical of both temperate fish (carp and trout) Hbs and AFHbs, assigned to the second CO coordination state, justifies the high auto-oxidation rate of fish Hbs. Furthermore, this novel CO coordination in AFHb occurs within a R-T intermediate quaternary structure. These findings provide an alternative structural explanation of the Root effect, in terms of a three state model .(5) This work was financially supported by PNRA (Italian National Programme for Antarctic Research) 1. Vergara, A., Franzese, M., Merlino, A., Vitagliano, L., di Prisco, G., Verde, C., Lee, H. C., Peisach, J., and Mazzarella, L. (2007) Biophys. J. 93, 2822-2829 2. Feng, L., Zhou, S., Gu, L., Gell, D., Mackay, J., ...
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spelling ftunivnapoliiris:oai:www.iris.unina.it:11588/346251 2025-01-16T19:12:23+00:00 Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states VERGARA, ALESSANDRO MERLINO, ANTONELLO L. Vitagliano G. Barbiero C. Verde G. di Prisco Lelio Mazzarella Vergara, Alessandro L., Vitagliano G., Barbiero Merlino, Antonello C., Verde G., di Prisco Lelio, Mazzarella 2008 ELETTRONICO http://hdl.handle.net/11588/346251 http://www.o2bip2008.dk/index.html eng eng country:DNK place:Aarhus ispartofbook:XIIIth European Conference on the Spectroscopy of Biological Molecules XIIIth European Conference on the Spectroscopy of Biological Molecules firstpage:P37 lastpage:P37 http://hdl.handle.net/11588/346251 http://www.o2bip2008.dk/index.html info:eu-repo/semantics/conferencePaper 2008 ftunivnapoliiris 2024-06-17T15:19:25Z All fish hemoglobins (Hb) show a high auto-oxidation rate, and some fish Hbs are endowed with Root effect (drastic drop of cooperativity at acidic pH). Differently from temperate fish Hbs, at physiological pH Antarctic fish Hbs (AFHbs) in the ferric state show both an aquomet form and two distinct hemichromes within a R / T intermediate quaternary structure (1). Interestingly, AFHbs exhibit a peroxidase activity higher than that observed for mammalian and temperate fish Hbs, thus suggesting that a partial hemichrome state in tetrameric Hbs does not protect them from peroxidation as previously proposed (2). At acidic pH, a combined EPR / x-ray crystallography approach has revealed, only for Root-effect AFHbs, significant amount of pentacoordinated (5C) high-spin Fe(III) species.(3) Furthermore, along the oxidation pathway, a combined x-ray crystallography / Resonance Raman spectroscopy of AFHbs has revealed a hybrid valence state [α(O2)/β(Fe3+, pentacoordinate)].(4) This valence hybrid states prompted us to test a FeSOD activity, that is as low as human Hb. A combined x-ray crystallography / FT-IR study has revealed at least two coordination states of the carbomonoxy form of AFHbs, one corresponding to a His assisted CO binding (band III at 1951 cm-1), and another to a not-His assisted CO binding (band IV at 1968 cm-1). The band IV, typical of both temperate fish (carp and trout) Hbs and AFHbs, assigned to the second CO coordination state, justifies the high auto-oxidation rate of fish Hbs. Furthermore, this novel CO coordination in AFHb occurs within a R-T intermediate quaternary structure. These findings provide an alternative structural explanation of the Root effect, in terms of a three state model .(5) This work was financially supported by PNRA (Italian National Programme for Antarctic Research) 1. Vergara, A., Franzese, M., Merlino, A., Vitagliano, L., di Prisco, G., Verde, C., Lee, H. C., Peisach, J., and Mazzarella, L. (2007) Biophys. J. 93, 2822-2829 2. Feng, L., Zhou, S., Gu, L., Gell, D., Mackay, J., ... Conference Object Antarc* Antarctic IRIS Università degli Studi di Napoli Federico II Antarctic Mackay ENVELOPE(168.517,168.517,-77.700,-77.700)
spellingShingle VERGARA, ALESSANDRO
MERLINO, ANTONELLO
L. Vitagliano
G. Barbiero
C. Verde
G. di Prisco
Lelio Mazzarella
Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states
title Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states
title_full Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states
title_fullStr Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states
title_full_unstemmed Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states
title_short Searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states
title_sort searching for additional functions of fish hemoglobins: evidence of multiple quaternary structures and exogeneous coordination states
url http://hdl.handle.net/11588/346251
http://www.o2bip2008.dk/index.html