Q-redox state: Difference between revisions

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ย  Communicated by [[Komlodi T]], [[Cardoso LHD]] 2020-07-28
ย  Communicated by [[Komlodi T]], [[Cardoso LHD]] 2020-07-28


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Revision as of 13:22, 20 November 2020


high-resolution terminology - matching measurements at high-resolution


Q-redox state

Description

The Q redox state reflects the redox status of the Q-junction in the mitochondrial or chloroplast electron transfer system (ETS). Ubiquinones, also known as coenzyme Q, and plastoquinones are essential mobile components of the mitochondria and chloroplasts that transfer electrons between the respiratory or photosynthetic complexes of the ETS. The Q redox state is dependent on the relative activities of the ETS enzymes that reduce and oxidize the quinones. Therefore, deficiencies in the mitochondrial ETS, originating from e.g. the malfunction of respiratory enzymes (complexes), can be detected by measuring the changes of the Q redox state with respect to respiratory activity.

Abbreviation: Qr/Qt


Calculation of the Q redox ratios

To analyze the Q redox state, SUIT protocols are designed with one step in which the Q is fully reduced and one in which it is fully oxidized. The values obtained will be used to calculate the Q redox ratios.

First, the signal is corrected for the fully oxidized Q state (Qox), which can be measured, e.g. in the presence of isolated mitochondria and CoQ2. (To fully oxidize the Q-pool rotenone can be added which inhibits respiration of endogenous substrates. However, it cannot be applied when NADH- or F-linked O2 flux is measured). Qox is then subtracted from the raw Q signal for every step before the calculation of the ratios:

Qr = Qraw-Qox

Then, the Q redox ratio is calculated between the given Q-signal in the presence of different substrates/inhibitors/uncouplers (Qr) and the fully reduced Q state (Qt, also corrected for Qox), which can be detected under anoxia for isolated mitochondria:

Qr/Qt

The Q-Module is part of the NextGen-O2k project

The Q-Module allows for monitoring of the redox state of electron transfer-reactive coenzyme Q at the Q-junction using the specific Q-Stoppers with the integrated three-electrode system and the modified electronics of the NextGen-O2k. Cyclic voltammetry is used for quality control and for defining the polarization voltage applied during Q-redox measurements.
Reference:
  • Komlรณdi T, Cardoso LHD, Doerrier C, Moore AL, Rich PR, Gnaiger E (2021) Coupling and pathway control of coenzyme Q redox state and respiration in isolated mitochondria. Bioenerg Commun 2021.3. https://doi.org/10.26124/bec:2021-0003
Communicated by Komlodi T, Cardoso LHD 2020-07-28
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Coenzyme Q
ยป Coenzyme Q
ยป Quinone, Ubiquinone Q; oxidized
ยป Quinol, Ubiquinol QH2; reduced
ยป Semiquinone
ยป Coenzyme Q2
ยป Q-redox state
ยป Q-pools
Mitochondrial pathways, respiratory Complexes, and Q
ยป Q-cycle
ยป Q-junction
ยป Convergent electron flow
ยป NS-pathway
ยป FNS
ยป FNSGp
ยป N-pathway
ยป Reverse electron flow from CII to CI
ยป CI
ยป Rotenone
ยป Amytal
ยป Piericidin
ยป S-pathway
ยป CII
ยป Malonate
ยป F-pathway
ยป CETF, Electron-transferring flavoprotein complex
ยป Gp-pathway
ยป CGpDH, Glycerophosphate dehydrogenase complex
ยป CIII
ยป Myxothiazol
ยป Choline dehydrogenase
ยป Dihydro-orotate dehydrogenase
NextGen-O2k and Q-Module
ยป NextGen-O2k
ยป Q-Module
ยป Q-Sensor
ยป Cyclic voltammetry
ยป Three-electrode system
General
ยป Categories of SUIT protocols
ยป Electron transfer pathway
ยป Electron-transfer-pathway state
ยป F-junction
ยป N-junction


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