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Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect
The discovery that cysteine (Cys) S-nitrosation of trout myoglobin (Mb) increases heme O(2) affinity has revealed a novel allosteric effect that may promote hypoxia-induced nitric oxide (NO) delivery in the trout heart and improve myocardial efficiency. To better understand this allosteric effect, w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039430/ https://www.ncbi.nlm.nih.gov/pubmed/24879536 http://dx.doi.org/10.1371/journal.pone.0097012 |
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author | Helbo, Signe Gow, Andrew J. Jamil, Amna Howes, Barry D. Smulevich, Giulietta Fago, Angela |
author_facet | Helbo, Signe Gow, Andrew J. Jamil, Amna Howes, Barry D. Smulevich, Giulietta Fago, Angela |
author_sort | Helbo, Signe |
collection | PubMed |
description | The discovery that cysteine (Cys) S-nitrosation of trout myoglobin (Mb) increases heme O(2) affinity has revealed a novel allosteric effect that may promote hypoxia-induced nitric oxide (NO) delivery in the trout heart and improve myocardial efficiency. To better understand this allosteric effect, we investigated the functional effects and structural origin of S-nitrosation in selected fish Mbs differing by content and position of reactive cysteine (Cys) residues. The Mbs from the Atlantic salmon and the yellowfin tuna, containing two and one reactive Cys, respectively, were S-nitrosated in vitro by reaction with Cys-NO to generate Mb-SNO to a similar yield (∼0.50 SH/heme), suggesting reaction at a specific Cys residue. As found for trout, salmon Mb showed a low O(2) affinity (P (50) = 2.7 torr) that was increased by S-nitrosation (P (50) = 1.7 torr), whereas in tuna Mb, O(2) affinity (P (50) = 0.9 torr) was independent of S-nitrosation. O(2) dissociation rates (k (off)) of trout and salmon Mbs were not altered when Cys were in the SNO or N-ethylmaleimide (NEM) forms, suggesting that S-nitrosation should affect O(2) affinity by raising the O(2) association rate (k (on)). Taken together, these results indicate that O(2)-linked S-nitrosation may occur specifically at Cys107, present in salmon and trout Mb but not in tuna Mb, and that it may relieve protein constraints that limit O(2) entry to the heme pocket of the unmodified Mb by a yet unknown mechanism. UV-Vis and resonance Raman spectra of the NEM-derivative of trout Mb (functionally equivalent to Mb-SNO and not photolabile) were identical to those of the unmodified Mb, indicating that S-nitrosation does not affect the extent or nature of heme-ligand stabilization of the fully ligated protein. The importance of S-nitrosation of Mb in vivo is confirmed by the observation that Mb-SNO is present in trout hearts and that its level can be significantly reduced by anoxic conditions. |
format | Online Article Text |
id | pubmed-4039430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40394302014-06-02 Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect Helbo, Signe Gow, Andrew J. Jamil, Amna Howes, Barry D. Smulevich, Giulietta Fago, Angela PLoS One Research Article The discovery that cysteine (Cys) S-nitrosation of trout myoglobin (Mb) increases heme O(2) affinity has revealed a novel allosteric effect that may promote hypoxia-induced nitric oxide (NO) delivery in the trout heart and improve myocardial efficiency. To better understand this allosteric effect, we investigated the functional effects and structural origin of S-nitrosation in selected fish Mbs differing by content and position of reactive cysteine (Cys) residues. The Mbs from the Atlantic salmon and the yellowfin tuna, containing two and one reactive Cys, respectively, were S-nitrosated in vitro by reaction with Cys-NO to generate Mb-SNO to a similar yield (∼0.50 SH/heme), suggesting reaction at a specific Cys residue. As found for trout, salmon Mb showed a low O(2) affinity (P (50) = 2.7 torr) that was increased by S-nitrosation (P (50) = 1.7 torr), whereas in tuna Mb, O(2) affinity (P (50) = 0.9 torr) was independent of S-nitrosation. O(2) dissociation rates (k (off)) of trout and salmon Mbs were not altered when Cys were in the SNO or N-ethylmaleimide (NEM) forms, suggesting that S-nitrosation should affect O(2) affinity by raising the O(2) association rate (k (on)). Taken together, these results indicate that O(2)-linked S-nitrosation may occur specifically at Cys107, present in salmon and trout Mb but not in tuna Mb, and that it may relieve protein constraints that limit O(2) entry to the heme pocket of the unmodified Mb by a yet unknown mechanism. UV-Vis and resonance Raman spectra of the NEM-derivative of trout Mb (functionally equivalent to Mb-SNO and not photolabile) were identical to those of the unmodified Mb, indicating that S-nitrosation does not affect the extent or nature of heme-ligand stabilization of the fully ligated protein. The importance of S-nitrosation of Mb in vivo is confirmed by the observation that Mb-SNO is present in trout hearts and that its level can be significantly reduced by anoxic conditions. Public Library of Science 2014-05-30 /pmc/articles/PMC4039430/ /pubmed/24879536 http://dx.doi.org/10.1371/journal.pone.0097012 Text en © 2014 Helbo et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Helbo, Signe Gow, Andrew J. Jamil, Amna Howes, Barry D. Smulevich, Giulietta Fago, Angela Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect |
title | Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect |
title_full | Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect |
title_fullStr | Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect |
title_full_unstemmed | Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect |
title_short | Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect |
title_sort | oxygen-linked s-nitrosation in fish myoglobins: a cysteine-specific tertiary allosteric effect |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039430/ https://www.ncbi.nlm.nih.gov/pubmed/24879536 http://dx.doi.org/10.1371/journal.pone.0097012 |
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