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Association of 2‐oxoacid dehydrogenase complexes with respirasomes in mitochondria.

Authors :
Plokhikh, Konstantin S.
Nesterov, Semen V.
Chesnokov, Yuriy M.
Rogov, Anton G.
Kamyshinsky, Roman A.
Vasiliev, Aleksandr L.
Yaguzhinsky, Lev S.
Vasilov, Raif G.
Source :
FEBS Journal. Jan2024, Vol. 291 Issue 1, p132-141. 10p.
Publication Year :
2024

Abstract

In the present study, cryo‐electron tomography was used to investigate the localization of 2‐oxoacid dehydrogenase complexes (OADCs) in cardiac mitochondria and mitochondrial inner membrane samples. Two classes of ordered OADC inner cores with different symmetries were distinguished and their quaternary structures modeled. One class corresponds to pyruvate dehydrogenase complexes and the other to dehydrogenase complexes of α‐ketoglutarate and branched‐chain α‐ketoacids. OADCs were shown to be localized in close proximity to membrane‐embedded respirasomes, as observed both in densely packed lamellar cristae of cardiac mitochondria and in ruptured mitochondrial samples where the dense packing is absent. This suggests the specificity of the OADC–respirasome interaction, which allows localized NADH/NAD+ exchange between OADCs and complex I of the respiratory chain. The importance of this local coupling is based on OADCs being the link between respiration, glycolysis and amino acid metabolism. The coupling of these basic metabolic processes can vary in different tissues and conditions and may be involved in the development of various pathologies. The present study shows that this important and previously missing parameter of mitochondrial complex coupling can be successfully assessed using cryo‐electron tomography. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1742464X
Volume :
291
Issue :
1
Database :
Academic Search Index
Journal :
FEBS Journal
Publication Type :
Academic Journal
Accession number :
174576931
Full Text :
https://doi.org/10.1111/febs.16965