Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II

The mitochondrial respiratory Complex II (CII) is one of key enzymes of cell energy metabolism, linking the tricarboxylic acid (TCA) cycle and the electron transport chain (ETC). CII reversibly oxidizes succinate to fumarate in the TCA cycle and transfers the electrons, produced by this reaction to...

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Main Authors: Nikolay I. Markevich, Miliausha H. Galimova, Lubov N. Markevich
Format: Article
Language:English
Published: Elsevier 2020-10-01
Series:Redox Biology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213231720308351
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spelling doaj-03216e51ff554e56a423ed85a042e2d12020-12-21T04:42:14ZengElsevierRedox Biology2213-23172020-10-0137101630Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex IINikolay I. Markevich0Miliausha H. Galimova1Lubov N. Markevich2Institute of Theoretical and Experimental Biophysics RAS, Pushchino, Moscow region, 142290, Russian Federation; Corresponding author. Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, 3 Institutskaya street, Pushchino, Moscow region, 14290, Russia.Institute of Theoretical and Experimental Biophysics RAS, Pushchino, Moscow region, 142290, Russian FederationInstitute of Cell Biophysics of RAS, Pushchino, Moscow region, 142290, Russian FederationThe mitochondrial respiratory Complex II (CII) is one of key enzymes of cell energy metabolism, linking the tricarboxylic acid (TCA) cycle and the electron transport chain (ETC). CII reversibly oxidizes succinate to fumarate in the TCA cycle and transfers the electrons, produced by this reaction to the membrane quinone pool, providing ubiquinol QH2 to ETC. CII is also known as a generator of reactive oxygen species (ROS).It was shown experimentally that succinate can serve as not only a substrate in the forward succinate-quinone oxidoreductase (SQR) direction, but also an enzyme activator. Molecular and kinetic mechanisms of this property of CII are still unclear.In order to account for activation of CII by succinate in the forward SQR direction, we developed and analyzed a computational mechanistic model of electron transfer and ROS formation in CII. It was found that re-binding of succinate to the unoccupied dicarboxylate binding site when FAD is reduced with subsequent oxidation of FADH2 creates a positive feedback loop in the succinate oxidation. The model predicts that this positive feedback can result in hysteresis and bistable switches in SQR activity and ROS production in CII. This requires that the rate constant of re-binding of succinate has to be higher than the rate constant of the initial succinate binding to the active center when FAD is oxidized.Hysteresis and bistability in the SQR activity and ROS production in CII can play an important physiological role. In the presence of hysteresis with two stable branches with high and low SQR activity, high SQR activity is maintained even with a very strong drop in the succinate concentration, which may be necessary in the process of cell functioning in stressful situations. For the same reason, a high stationary rate of ROS production in CII can be maintained at low succinate concentrations.http://www.sciencedirect.com/science/article/pii/S2213231720308351Complex IIReactive oxygen species (ROS)Computational modelHysteresisBistability
collection DOAJ
language English
format Article
sources DOAJ
author Nikolay I. Markevich
Miliausha H. Galimova
Lubov N. Markevich
spellingShingle Nikolay I. Markevich
Miliausha H. Galimova
Lubov N. Markevich
Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II
Redox Biology
Complex II
Reactive oxygen species (ROS)
Computational model
Hysteresis
Bistability
author_facet Nikolay I. Markevich
Miliausha H. Galimova
Lubov N. Markevich
author_sort Nikolay I. Markevich
title Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II
title_short Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II
title_full Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II
title_fullStr Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II
title_full_unstemmed Hysteresis and bistability in the succinate-CoQ reductase activity and reactive oxygen species production in the mitochondrial respiratory complex II
title_sort hysteresis and bistability in the succinate-coq reductase activity and reactive oxygen species production in the mitochondrial respiratory complex ii
publisher Elsevier
series Redox Biology
issn 2213-2317
publishDate 2020-10-01
description The mitochondrial respiratory Complex II (CII) is one of key enzymes of cell energy metabolism, linking the tricarboxylic acid (TCA) cycle and the electron transport chain (ETC). CII reversibly oxidizes succinate to fumarate in the TCA cycle and transfers the electrons, produced by this reaction to the membrane quinone pool, providing ubiquinol QH2 to ETC. CII is also known as a generator of reactive oxygen species (ROS).It was shown experimentally that succinate can serve as not only a substrate in the forward succinate-quinone oxidoreductase (SQR) direction, but also an enzyme activator. Molecular and kinetic mechanisms of this property of CII are still unclear.In order to account for activation of CII by succinate in the forward SQR direction, we developed and analyzed a computational mechanistic model of electron transfer and ROS formation in CII. It was found that re-binding of succinate to the unoccupied dicarboxylate binding site when FAD is reduced with subsequent oxidation of FADH2 creates a positive feedback loop in the succinate oxidation. The model predicts that this positive feedback can result in hysteresis and bistable switches in SQR activity and ROS production in CII. This requires that the rate constant of re-binding of succinate has to be higher than the rate constant of the initial succinate binding to the active center when FAD is oxidized.Hysteresis and bistability in the SQR activity and ROS production in CII can play an important physiological role. In the presence of hysteresis with two stable branches with high and low SQR activity, high SQR activity is maintained even with a very strong drop in the succinate concentration, which may be necessary in the process of cell functioning in stressful situations. For the same reason, a high stationary rate of ROS production in CII can be maintained at low succinate concentrations.
topic Complex II
Reactive oxygen species (ROS)
Computational model
Hysteresis
Bistability
url http://www.sciencedirect.com/science/article/pii/S2213231720308351
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