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Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values
Studies are reported on the formation of low-spin six-coordinate [Fe(PPIX)L(2)] complexes from iron(II) protoporphyrin where L is one of a series of nitrogenous ligands (aliphatic, aromatic or heterocyclic). The bonding constants have been determined by titration of the metal complex with these liga...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960585/ https://www.ncbi.nlm.nih.gov/pubmed/35235042 http://dx.doi.org/10.1007/s00775-022-01929-4 |
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author | Silver, Jack Al-Jaff, Golzar Wilson, Michael T. den Engelsen, Daniel Fern, George R. Ireland, Terry G. |
author_facet | Silver, Jack Al-Jaff, Golzar Wilson, Michael T. den Engelsen, Daniel Fern, George R. Ireland, Terry G. |
author_sort | Silver, Jack |
collection | PubMed |
description | Studies are reported on the formation of low-spin six-coordinate [Fe(PPIX)L(2)] complexes from iron(II) protoporphyrin where L is one of a series of nitrogenous ligands (aliphatic, aromatic or heterocyclic). The bonding constants have been determined by titration of the metal complex with these ligands and are compared in relation to previous studies. The adduct formation was monitored utilising optical spectroscopy. In addition, Mӧssbauer spectroscopic experiments were conducted to monitor the electronic environment around the central iron atom in these complexes. The two complementary spectroscopic methods indicated that all nitrogen ligands formed low-spin octahedral complexes. The magnitude of the overall binding constants (β(2) values) are discussed and related to (a) the pK(a) values of the free ligands and (b) the Mössbauer parameter ΔE(Q), which represents the quadrupole splitting of the haem iron. The β(2) and ΔE(Q) values are also discussed in terms of the structure of the ligand. Cooperative binding was observed for nearly all the ligands with Hill coefficients close to 2 for iron(II) protoporphyrin; one of these ligands displayed a much greater affinity than any we previously studied, and this was a direct consequence of the structure of the ligand. Overall conclusions on these and previous studies are drawn in terms of aliphatic ligands versus aromatic ring structures and the absence or presence of sterically hindered nitrogen atoms. The implications of the work for the greater understanding of haem proteins in general and in particular how the nitrogenous ligand binding results are relevant to and aid the understanding of the binding of inhibitor molecules to the cytochrome P(450) mono-oxygenases (for therapeutic purposes) are also discussed. GRAPHICAL ABSTRACT: Changes in the electronic absorption spectra of five-coordinate [Fe(II)(PPIX)(2-MeIm)] that occurred as the temperature was lowered from room temperature to 78° K [Image: see text] |
format | Online Article Text |
id | pubmed-8960585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-89605852022-04-07 Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values Silver, Jack Al-Jaff, Golzar Wilson, Michael T. den Engelsen, Daniel Fern, George R. Ireland, Terry G. J Biol Inorg Chem Original Paper Studies are reported on the formation of low-spin six-coordinate [Fe(PPIX)L(2)] complexes from iron(II) protoporphyrin where L is one of a series of nitrogenous ligands (aliphatic, aromatic or heterocyclic). The bonding constants have been determined by titration of the metal complex with these ligands and are compared in relation to previous studies. The adduct formation was monitored utilising optical spectroscopy. In addition, Mӧssbauer spectroscopic experiments were conducted to monitor the electronic environment around the central iron atom in these complexes. The two complementary spectroscopic methods indicated that all nitrogen ligands formed low-spin octahedral complexes. The magnitude of the overall binding constants (β(2) values) are discussed and related to (a) the pK(a) values of the free ligands and (b) the Mössbauer parameter ΔE(Q), which represents the quadrupole splitting of the haem iron. The β(2) and ΔE(Q) values are also discussed in terms of the structure of the ligand. Cooperative binding was observed for nearly all the ligands with Hill coefficients close to 2 for iron(II) protoporphyrin; one of these ligands displayed a much greater affinity than any we previously studied, and this was a direct consequence of the structure of the ligand. Overall conclusions on these and previous studies are drawn in terms of aliphatic ligands versus aromatic ring structures and the absence or presence of sterically hindered nitrogen atoms. The implications of the work for the greater understanding of haem proteins in general and in particular how the nitrogenous ligand binding results are relevant to and aid the understanding of the binding of inhibitor molecules to the cytochrome P(450) mono-oxygenases (for therapeutic purposes) are also discussed. GRAPHICAL ABSTRACT: Changes in the electronic absorption spectra of five-coordinate [Fe(II)(PPIX)(2-MeIm)] that occurred as the temperature was lowered from room temperature to 78° K [Image: see text] Springer International Publishing 2022-03-02 2022 /pmc/articles/PMC8960585/ /pubmed/35235042 http://dx.doi.org/10.1007/s00775-022-01929-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Silver, Jack Al-Jaff, Golzar Wilson, Michael T. den Engelsen, Daniel Fern, George R. Ireland, Terry G. Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values |
title | Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values |
title_full | Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values |
title_fullStr | Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values |
title_full_unstemmed | Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values |
title_short | Studies on the binding of nitrogenous bases to protoporphyrin IX iron(II) in aqueous solution at high pH values |
title_sort | studies on the binding of nitrogenous bases to protoporphyrin ix iron(ii) in aqueous solution at high ph values |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960585/ https://www.ncbi.nlm.nih.gov/pubmed/35235042 http://dx.doi.org/10.1007/s00775-022-01929-4 |
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