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Annals of Clinical and Translational Neurology 2017-12

4-Hydroxybenzoic acid restores CoQ10 biosynthesis in human COQ2 deficiency.

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Diran Herebian
Annette Seibt
Sander H J Smits
Richard J Rodenburg
Ertan Mayatepek
Felix Distelmaier

Nøgleord

Abstrakt

The clinical phenotypes of human CoQ10-deficiency caused by COQ2 mutations range from fatal neonatal disease to adult-onset multisystem atrophy. So far, treatment options for these diseases are unsatisfactory. Here, we demonstrate that supplementation of 4-hydroxybenzoic acid (4-HBA) fully restores endogenous CoQ10-biosynthesis in COQ2-deficient cell lines. This was accompanied by increased protein expression of CoQ10-biosynthesis-enzymes as well as a rescue of cell viability during stress conditions. In silico analysis suggested a ligand transportation path for 4-HBA through the COQ2 protein towards the mitochondrial matrix side. This process is apparently hindered by disease-causing mutations, which can be overcome by increasing 4-HBA concentrations.

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