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HDQ (1-hydroxy-2-dodecyl-4(1H)quinolone), a high affinity inhibitor for mitochondrial alternative NADH dehydrogenase: evidence for a ping-pong mechanism.

作者信息

Eschemann Andrea, Galkin Alexander, Oettmeier Walter, Brandt Ulrich, Kerscher Stefan

机构信息

Universität Frankfurt, Fachbereich Medizin, Institut für Biochemie I, Frankfurt am Main D-60490, Germany.

出版信息

J Biol Chem. 2005 Feb 4;280(5):3138-42. doi: 10.1074/jbc.M411217200. Epub 2004 Nov 8.

Abstract

Alternative NADH dehydrogenases (NADH:ubiquinone oxidoreductases) are single subunit respiratory chain enzymes found in plant and fungal mitochondria and in many bacteria. It is unclear how these peripheral membrane proteins interact with their hydrophobic substrate ubiquinone. Known inhibitors of alternative NADH dehydrogenases bind with rather low affinities. We have identified 1-hydroxy-2-dodecyl-4(1H)quinolone as a high affinity inhibitor of alternative NADH dehydrogenase from Yarrowia lipolytica. Using this compound, we have analyzed the bisubstrate and inhibition kinetics for NADH and decylubiquinone. We found that the kinetics of alternative NADH dehydrogenase follow a ping-pong mechanism. This suggests that NADH and the ubiquinone headgroup interact with the same binding pocket in an alternating fashion.

摘要

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