Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Difference between revisions of "Cardoso 2022 Abstract Bioblast"

From Bioblast
Line 19: Line 19:
:::: This work was part of the Oroboros [[NextGen-O2k]] project, with funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement nº 859770.
:::: This work was part of the Oroboros [[NextGen-O2k]] project, with funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement nº 859770.


== Help ==
== List of abbreviations, terms and definitions - MitoPedia ==
* [[MitoPedia: Terms and abbreviations]]
{{Template:List of abbreviations, terms and definitions - MitoPedia}}


{{Labeling
{{Labeling

Revision as of 12:26, 28 May 2022

Bioblast2022 banner.jpg

Luiza Cardoso
Cardoso Luiza HD, Doerrier C, Donnelly C, Komlódi T, Gnaiger E (2022) Redox monitoring and respiration - a new horizon with the NextGen-O2k. Bioblast 2022: BEC Inaugural Conference.

Link: Bioblast 2022: BEC Inaugural Conference

Cardoso Luiza HD, Doerrier Carolina, Donnelly Chris, Komlódi Timea, Gnaiger Erich (2022)

Event: Bioblast 2022

NADH-linked substrates (N-substrates) of TCA-cycle and other mt-matrix dehydrogenases feed electrons through the N-junction into Complex I. The redox states of the NAD-pool — defined as the sum of NAD(P)+ and NAD(P)H — and of the electron transfer system (ETS)-reactive coenzyme Q-pool [1] are linked in the N-pathway but are regulated independently by several convergent electron entries into the Q-junction [2]. Our results obtained with HRR and the NADH- and Q-Modules of the NextGen-O2k show that complementary to ET-pathway control of respiratory rate and redox state (redox push by electron input), coupling control exerts opposite effects on the metabolic parameters. Whereas redox push reduces the N- and Q-pool in the LEAK state at low O2 flux and high protonomotive force pmF, stimulation of O2 flux by ADP in the OXPHOS state [3] is accompanied by a redox pull to the oxidized state. Under these conditions, ET-pathways converging at the Q-junction yield partial additivity of O2 flux, when ET-capacity downstream of Q and phosphorylation capacity exert flux control [2]. Monitoring of respiration together with NAD(P)H autofluorescence and Q-redox state [1] provides unique analytical and diagnostic power in the study of mitochondrial respiratory control at the N- and Q-junctions.

  1. Komlódi 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
  2. Gnaiger E (2020) Mitochondrial pathways and respiratory control. An introduction to OXPHOS analysis. 5th ed. Bioenerg Commun 2020.2. https://doi.org/10.26124/bec:2020-0002
  3. Gnaiger E et al ― MitoEAGLE Task Group (2020) Mitochondrial physiology. Bioenerg Commun 2020.1. https://doi.org/10.26124/bec:2020-0001.v1


O2k-Network Lab: AT Innsbruck Oroboros


Affiliations and support

Oroboros Instruments GmbH, Innsbruck, Austria
This work was part of the Oroboros NextGen-O2k project, with funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement nº 859770.

List of abbreviations, terms and definitions - MitoPedia

» MitoPedia: Terms and abbreviations


Labels: MiParea: Respiration 


Organism: Mouse  Tissue;cell: Liver, HEK  Preparation: Permeabilized cells, Isolated mitochondria 


Coupling state: LEAK, OXPHOS, ET  Pathway: N, S, NS, ROX  HRR: Oxygraph-2k, NextGen-O2k