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Difference between revisions of "Makrecka-Kuka 2015 Biomolecules"

From Bioblast
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|year=2015
|year=2015
|journal=Biomolecules
|journal=Biomolecules
|abstract=Whereas mitochondria are well established as the source of ATP in the process of oxidative phosphorylation (OXPHOS), it is debated if they are also the major sources of reactive oxygen species (ROS). Here we describe the novel approach of combining high-resolution respirometry and fluorometric measurement of hydrogen peroxide (H2O2) production, applied to mitochondrial preparations (permeabilized cells, tissue homogenate, isolated mitochondria). The widely used H2O2 probe Amplex red inhibited respiration in intact and permeabilized cells and should not be applied at concentrations above 10 µM. H2O2 fluxes were generally less than 1% of oxygen fluxes in physiological substrate and coupling states, specifically in permeabilized cells. H2O2 flux was consistently highest in the Complex II-linked LEAK state, reduced with CI&II-linked convergent electron  flow and in mitochondria respiring at OXPHOS capacity, and were further diminished in uncoupled mitochondria respiring at electron transfer system capacity. Simultaneous measurement of mitochondrial respiration and H2O2 flux requires careful optimization of assay conditions and reveals information in functional OXPHOS analysis beyond these assays carried out separately.
|abstract=Whereas mitochondria are well established as the source of ATP in the process of oxidative phosphorylation (OXPHOS), it is debated if they are also the major sources of reactive oxygen species (ROS). Here we describe the novel approach of combining high-resolution respirometry and fluorometric measurement of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) production, applied to mitochondrial preparations (permeabilized cells, tissue homogenate, isolated mitochondria). The widely used H<sub>2</sub>O<sub>2</sub> probe Amplex red inhibited respiration in intact and permeabilized cells and should not be applied at concentrations above 10 µM. H<sub>2</sub>O<sub>2</sub> fluxes were generally less than 1% of oxygen fluxes in physiological substrate and coupling states, specifically in permeabilized cells. H<sub>2</sub>O<sub>2</sub> flux was consistently highest in the Complex II-linked LEAK state, reduced with CI&II-linked convergent electron  flow and in mitochondria respiring at OXPHOS capacity, and were further diminished in uncoupled mitochondria respiring at electron transfer system capacity. Simultaneous measurement of mitochondrial respiration and H<sub>2</sub>O<sub>2</sub> flux requires careful optimization of assay conditions and reveals information in functional OXPHOS analysis beyond these assays carried out separately.
|keywords=High-resolution respirometry, H2O2 flux, Amplex Red, HEK 293T, Mouse brain homogenate,  Mouse cardiac mitochondria
|keywords=High-resolution respirometry, H<sub>2</sub>O<sub>2</sub> flux, Amplex Red, HEK 293T, Mouse brain homogenate,  Mouse cardiac mitochondria
|mipnetlab=AT Innsbruck OROBOROS, AT Innsbruck Gnaiger E
|mipnetlab=AT Innsbruck OROBOROS, AT Innsbruck Gnaiger E
}}
}}

Revision as of 08:29, 9 June 2015

Publications in the MiPMap
O2k-Protocols contents

Makrecka-Kuka M, Krumschnabel G, Gnaiger E (2015) High-resolution respirometry for simultaneous measurement of oxygen and hydrogen peroxide fluxes in permeabilized cells, tissue homogenate and isolated mitochondria. Biomolecules doi:10.3390/biom40x000x.

» Open Access

Makrecka-Kuka M, Krumschnabel G, Gnaiger E (2015) Biomolecules

Abstract: Whereas mitochondria are well established as the source of ATP in the process of oxidative phosphorylation (OXPHOS), it is debated if they are also the major sources of reactive oxygen species (ROS). Here we describe the novel approach of combining high-resolution respirometry and fluorometric measurement of hydrogen peroxide (H2O2) production, applied to mitochondrial preparations (permeabilized cells, tissue homogenate, isolated mitochondria). The widely used H2O2 probe Amplex red inhibited respiration in intact and permeabilized cells and should not be applied at concentrations above 10 µM. H2O2 fluxes were generally less than 1% of oxygen fluxes in physiological substrate and coupling states, specifically in permeabilized cells. H2O2 flux was consistently highest in the Complex II-linked LEAK state, reduced with CI&II-linked convergent electron flow and in mitochondria respiring at OXPHOS capacity, and were further diminished in uncoupled mitochondria respiring at electron transfer system capacity. Simultaneous measurement of mitochondrial respiration and H2O2 flux requires careful optimization of assay conditions and reveals information in functional OXPHOS analysis beyond these assays carried out separately. Keywords: High-resolution respirometry, H2O2 flux, Amplex Red, HEK 293T, Mouse brain homogenate, Mouse cardiac mitochondria

O2k-Network Lab: AT Innsbruck OROBOROS, AT Innsbruck Gnaiger E


Labels: MiParea: Respiration, Instruments;methods 


Organism: Human, Mouse  Tissue;cell: Heart  Preparation: Intact cells, Permeabilized cells, Homogenate, Isolated mitochondria 


Coupling state: LEAK, ROUTINE, OXPHOS, ETS"ETS" is not in the list (LEAK, ROUTINE, OXPHOS, ET) of allowed values for the "Coupling states" property. 

HRR: Oxygraph-2k, O2k-Fluorometer, Protocol"Protocol" is not in the list (Oxygraph-2k, TIP2k, O2k-Fluorometer, pH, NO, TPP, Ca, O2k-Spectrophotometer, O2k-Manual, O2k-Protocol, ...) of allowed values for the "Instrument and method" property. 

O2k-Demo, O2k-MultiSensor