Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with Penicillamine

This paper describes a comparative study of the decomposition of two nitrosyl iron complexes (NICs) with penicillamine thiolic ligands [Fe2(SC5H11NO2)2(NO)4]SO4·5H2O (I) and glutathione- (GSH-) ligands [Fe2(SC10H17N3O6)2(NO)4]SO4·2H2O (II), which spontaneously evolve to NO in aqueous medium. NO form...

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Main Authors: Lidia Syrtsova, Natalia Sanina, Konstantin Lyssenko, Evgeniy Kabachkov, Boris Psikha, Natal’ja Shkondina, Olesia Pokidova, Alexander Kotelnikov, Sergey Aldoshin
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Bioinorganic Chemistry and Applications
Online Access:http://dx.doi.org/10.1155/2014/641407
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author Lidia Syrtsova
Natalia Sanina
Konstantin Lyssenko
Evgeniy Kabachkov
Boris Psikha
Natal’ja Shkondina
Olesia Pokidova
Alexander Kotelnikov
Sergey Aldoshin
author_facet Lidia Syrtsova
Natalia Sanina
Konstantin Lyssenko
Evgeniy Kabachkov
Boris Psikha
Natal’ja Shkondina
Olesia Pokidova
Alexander Kotelnikov
Sergey Aldoshin
author_sort Lidia Syrtsova
collection DOAJ
description This paper describes a comparative study of the decomposition of two nitrosyl iron complexes (NICs) with penicillamine thiolic ligands [Fe2(SC5H11NO2)2(NO)4]SO4·5H2O (I) and glutathione- (GSH-) ligands [Fe2(SC10H17N3O6)2(NO)4]SO4·2H2O (II), which spontaneously evolve to NO in aqueous medium. NO formation was measured by a sensor electrode and by spectrophotometric methods by measuring the formation of a hemoglobin- (Hb-) NO complex. The NO evolution reaction rate from (I)  k1 = (4.6 ± 0.1)·10−3 s−1 and the elimination rate constant of the penicillamine ligand k2 = (1.8 ± 0.2)·10−3 s−1 at 25°C in 0.05 M phosphate buffer,  pH 7.0, was calculated using kinetic modeling based on the experimental data. Both reactions are reversible. Spectrophotometry and mass-spectrometry methods have firmly shown that the penicillamine ligand is exchanged for GS− during decomposition of 1.5·10−4 M (I) in the presence of 10−3 M GSH, with 76% yield in 24 h. As has been established, such behaviour is caused by the resistance of (II) to decomposition due to the higher affinity of iron to GSH in the complex. The discovered reaction may impede S-glutathionylation of the essential enzyme systems in the presence of (I) and is important for metabolism of NIC, connected with its antitumor activity.
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institution Kabale University
issn 1565-3633
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language English
publishDate 2014-01-01
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spelling doaj-art-8b301d30470f4e24b3df471a004e97ff2025-08-20T03:37:33ZengWileyBioinorganic Chemistry and Applications1565-36331687-479X2014-01-01201410.1155/2014/641407641407Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with PenicillamineLidia Syrtsova0Natalia Sanina1Konstantin Lyssenko2Evgeniy Kabachkov3Boris Psikha4Natal’ja Shkondina5Olesia Pokidova6Alexander Kotelnikov7Sergey Aldoshin8Institute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaA.N. Nesmeyanov Institute of Organoelement Compounds of RAS, 28 Vavilov Street, B-334, Moscow 119991, RussiaInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, Academician Semenov Avenue Chernogolovka, Moscow Region 142432, RussiaThis paper describes a comparative study of the decomposition of two nitrosyl iron complexes (NICs) with penicillamine thiolic ligands [Fe2(SC5H11NO2)2(NO)4]SO4·5H2O (I) and glutathione- (GSH-) ligands [Fe2(SC10H17N3O6)2(NO)4]SO4·2H2O (II), which spontaneously evolve to NO in aqueous medium. NO formation was measured by a sensor electrode and by spectrophotometric methods by measuring the formation of a hemoglobin- (Hb-) NO complex. The NO evolution reaction rate from (I)  k1 = (4.6 ± 0.1)·10−3 s−1 and the elimination rate constant of the penicillamine ligand k2 = (1.8 ± 0.2)·10−3 s−1 at 25°C in 0.05 M phosphate buffer,  pH 7.0, was calculated using kinetic modeling based on the experimental data. Both reactions are reversible. Spectrophotometry and mass-spectrometry methods have firmly shown that the penicillamine ligand is exchanged for GS− during decomposition of 1.5·10−4 M (I) in the presence of 10−3 M GSH, with 76% yield in 24 h. As has been established, such behaviour is caused by the resistance of (II) to decomposition due to the higher affinity of iron to GSH in the complex. The discovered reaction may impede S-glutathionylation of the essential enzyme systems in the presence of (I) and is important for metabolism of NIC, connected with its antitumor activity.http://dx.doi.org/10.1155/2014/641407
spellingShingle Lidia Syrtsova
Natalia Sanina
Konstantin Lyssenko
Evgeniy Kabachkov
Boris Psikha
Natal’ja Shkondina
Olesia Pokidova
Alexander Kotelnikov
Sergey Aldoshin
Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with Penicillamine
Bioinorganic Chemistry and Applications
title Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with Penicillamine
title_full Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with Penicillamine
title_fullStr Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with Penicillamine
title_full_unstemmed Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with Penicillamine
title_short Reversible Dissociation and Ligand-Glutathione Exchange Reaction in Binuclear Cationic Tetranitrosyl Iron Complex with Penicillamine
title_sort reversible dissociation and ligand glutathione exchange reaction in binuclear cationic tetranitrosyl iron complex with penicillamine
url http://dx.doi.org/10.1155/2014/641407
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