The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase
The interaction of the superoxide radical ion O2 – with the active site of Cu, Zn-superoxide dismutase is studied by computer simulation using the ORCA software package version 5.0.2 at the level of density functional theory using the PBE functional and the basis sets of functions def2-SVP, def2-SVP...
Published in: | Bulletin of the Karaganda University. "Chemistry" series |
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Academician Ye.A. Buketov Karaganda University
2022
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ftdoajarticles:oai:doaj.org/article:5f34edf89bf54b1dbe1825710fded808 2023-05-15T17:53:53+02:00 The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase A.V. Ryabykh O.A. Maslova S.A. Beznosyuk A.S. Masalimov 2022-06-01T00:00:00Z https://doi.org/10.31489/2022Ch2/2-22-20 https://doaj.org/article/5f34edf89bf54b1dbe1825710fded808 EN eng Academician Ye.A. Buketov Karaganda University https://chemistry-vestnik.ksu.kz/apart/2022-106-2/09.pdf https://doaj.org/toc/2663-4872 doi:10.31489/2022Ch2/2-22-20 2663-4872 https://doaj.org/article/5f34edf89bf54b1dbe1825710fded808 Қарағанды университетінің хабаршысы. Химия сериясы, Vol 106, Iss 2, Pp 77-86 (2022) cu zn-superoxide dismutase superoxide radical ion enzyme reactive oxygen species antioxidants condensed state physical chemistry computer simulation Chemistry QD1-999 article 2022 ftdoajarticles https://doi.org/10.31489/2022Ch2/2-22-20 2022-12-31T00:41:27Z The interaction of the superoxide radical ion O2 – with the active site of Cu, Zn-superoxide dismutase is studied by computer simulation using the ORCA software package version 5.0.2 at the level of density functional theory using the PBE functional and the basis sets of functions def2-SVP, def2-SVPD and def2-TZVPD. The main characteristics for two processes of electron transfer in the catalytic cycle of radical ion deactivation are obtained: reaction potential ΔG0, total reorganization energy λtot, activation energy ΔG≠, overlap matrix element HDA, and transfer rate constant k according to Marcus. The variable factor in the modeling is the presence of the Zn2+ ion at the active site of the enzyme. Two variants of the electron transfer mechanism are considered: one carried out through ligands and another occurring in the immediate vicinity of an oxygencontaining particle and a copper ion. It has been established that the presence of the Zn2+ ion contributes to a large extent only to the second electron transfer from the Cu+ ion to the protonated form of the radical ion, to the hydroperoxide radical HO2. Other things being equal, the zinc ion increases the electron transfer rate constant by five times through specific interactions. Article in Journal/Newspaper Orca Directory of Open Access Journals: DOAJ Articles Bulletin of the Karaganda University. "Chemistry" series 106 2 77 86 |
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cu zn-superoxide dismutase superoxide radical ion enzyme reactive oxygen species antioxidants condensed state physical chemistry computer simulation Chemistry QD1-999 |
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cu zn-superoxide dismutase superoxide radical ion enzyme reactive oxygen species antioxidants condensed state physical chemistry computer simulation Chemistry QD1-999 A.V. Ryabykh O.A. Maslova S.A. Beznosyuk A.S. Masalimov The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase |
topic_facet |
cu zn-superoxide dismutase superoxide radical ion enzyme reactive oxygen species antioxidants condensed state physical chemistry computer simulation Chemistry QD1-999 |
description |
The interaction of the superoxide radical ion O2 – with the active site of Cu, Zn-superoxide dismutase is studied by computer simulation using the ORCA software package version 5.0.2 at the level of density functional theory using the PBE functional and the basis sets of functions def2-SVP, def2-SVPD and def2-TZVPD. The main characteristics for two processes of electron transfer in the catalytic cycle of radical ion deactivation are obtained: reaction potential ΔG0, total reorganization energy λtot, activation energy ΔG≠, overlap matrix element HDA, and transfer rate constant k according to Marcus. The variable factor in the modeling is the presence of the Zn2+ ion at the active site of the enzyme. Two variants of the electron transfer mechanism are considered: one carried out through ligands and another occurring in the immediate vicinity of an oxygencontaining particle and a copper ion. It has been established that the presence of the Zn2+ ion contributes to a large extent only to the second electron transfer from the Cu+ ion to the protonated form of the radical ion, to the hydroperoxide radical HO2. Other things being equal, the zinc ion increases the electron transfer rate constant by five times through specific interactions. |
format |
Article in Journal/Newspaper |
author |
A.V. Ryabykh O.A. Maslova S.A. Beznosyuk A.S. Masalimov |
author_facet |
A.V. Ryabykh O.A. Maslova S.A. Beznosyuk A.S. Masalimov |
author_sort |
A.V. Ryabykh |
title |
The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase |
title_short |
The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase |
title_full |
The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase |
title_fullStr |
The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase |
title_full_unstemmed |
The Role of Zinc Ion in the Active Site of Copper-Zinc Superoxide Dismutase |
title_sort |
role of zinc ion in the active site of copper-zinc superoxide dismutase |
publisher |
Academician Ye.A. Buketov Karaganda University |
publishDate |
2022 |
url |
https://doi.org/10.31489/2022Ch2/2-22-20 https://doaj.org/article/5f34edf89bf54b1dbe1825710fded808 |
genre |
Orca |
genre_facet |
Orca |
op_source |
Қарағанды университетінің хабаршысы. Химия сериясы, Vol 106, Iss 2, Pp 77-86 (2022) |
op_relation |
https://chemistry-vestnik.ksu.kz/apart/2022-106-2/09.pdf https://doaj.org/toc/2663-4872 doi:10.31489/2022Ch2/2-22-20 2663-4872 https://doaj.org/article/5f34edf89bf54b1dbe1825710fded808 |
op_doi |
https://doi.org/10.31489/2022Ch2/2-22-20 |
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Bulletin of the Karaganda University. "Chemistry" series |
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106 |
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77 |
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