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...

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Published in:Bulletin of the Karaganda University. "Chemistry" series
Main Authors: A.V. Ryabykh, O.A. Maslova, S.A. Beznosyuk, A.S. Masalimov
Format: Article in Journal/Newspaper
Language:English
Published: Academician Ye.A. Buketov Karaganda University 2022
Subjects:
Online Access:https://doi.org/10.31489/2022Ch2/2-22-20
https://doaj.org/article/5f34edf89bf54b1dbe1825710fded808
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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
collection Directory of Open Access Journals: DOAJ Articles
container_issue 2
container_start_page 77
container_title Bulletin of the Karaganda University. "Chemistry" series
container_volume 106
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.
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op_doi https://doi.org/10.31489/2022Ch2/2-22-20
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
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https://doaj.org/article/5f34edf89bf54b1dbe1825710fded808
op_source Қарағанды университетінің хабаршысы. Химия сериясы, Vol 106, Iss 2, Pp 77-86 (2022)
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spelling ftdoajarticles:oai:doaj.org/article:5f34edf89bf54b1dbe1825710fded808 2025-01-17T00:10:18+00:00 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
spellingShingle 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
title 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_short 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
topic cu
zn-superoxide dismutase
superoxide radical ion
enzyme
reactive oxygen species
antioxidants
condensed state physical chemistry
computer simulation
Chemistry
QD1-999
topic_facet cu
zn-superoxide dismutase
superoxide radical ion
enzyme
reactive oxygen species
antioxidants
condensed state physical chemistry
computer simulation
Chemistry
QD1-999
url https://doi.org/10.31489/2022Ch2/2-22-20
https://doaj.org/article/5f34edf89bf54b1dbe1825710fded808