Mitochondria efficiently adapt to changing metabolic conditions

Cellular respiration of the inner mitochondrial membrane

Mitochondria, the power plants of the cell, make massive contributions to the energy supply of the body by burning metabolites with the help of oxygen. This cellular respiration takes place in the inner of the two mitochondrial membranes that, in contrast to the outer membrane, is strongly folded. The structure and topology of these membrane folds, the so-called cristae membranes, has profound influence on the efficiency of respiration and is important for many mitochondrial functions. For this reason, cristae architecture is controlled precisely and adapted dynamically to changes in cellular metabolism. Defects in these processes result in severe human diseases.

Communication is key

Two protein complexes in the inner mitochondrial membrane that are required for a normal membrane architecture are the F1Fo-ATP synthase, an enzyme that also participates in energy conversion, and the MICOS complex (mitochondrial contact site and cristae organizing system). These complexes are regarded as antagonists; they are localized in different areas of the inner membrane and bend the membrane in opposite directions. It was unclear how the functions of these two protein complexes can be coordinated with each other. The team around Rampelt and Pfanner now demonstrate that MICOS and ATP synthase communicate with each other and that this is vital for healthy mitochondrial function. A MICOS subunit, Mic10, travels to the ATP synthase and stabilizes the association of several ATP synthases to large complexes. This new regulatory function of Mic10 is pivotal for efficient metabolic adaptation and respiratory growth. “Communication between the two complexes is likely key to the coordinated biogenesis of the inner mitochondrial membrane,” explains Rampelt.

Heike Rampelt, Nikolaus Pfanner and Claudine Kraft lead research groups at the Institute of Biochemistry and Molecular Biology of the Medical Faculty and perform research in the Excellence Cluster CIBSS of the University Freiburg in the area of biological signalling studies.

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