Assay conditions for the mitochondrial NADH:coenzyme Q oxidoreductase
Open Access
- 11 October 1993
- journal article
- research article
- Published by Wiley in FEBS Letters
- Vol. 332 (1-2) , 127-131
- https://doi.org/10.1016/0014-5793(93)80498-j
Abstract
The assay of Complex I activity requires the use of artificial acceptors, such as short‐chain coenzyme Q homologs and analogs, because the physiological quinones, such as CoQ10, are too insoluble in water to be added as substrates to the assay media. The medical interest raised in the last years on the pathological changes of Complex I activity has focussed on the requirement of easy reliable assays for its analysis. We have undertaken a systematic examination of the assay conditions of Complex I in mitochondrial membranes, using a series of quinones as electron acceptors, particularly the coenzyme Q homologs CoQ0, CoQ1 and CoQ2, and the analogs duroquinone and decylubiquinone. Our findings have pointed out that the most suitable electron acceptor for the NADH:CoQ reductase assay is the homolog CoQ1. The analog DB, commercially available, although yielding a high activity, nevertheless causes some problems for the standardization of the assay conditions.Keywords
This publication has 19 references indexed in Scilit:
- Complex I and Complex III of Mitochondria Have Common Inhibitors Acting as Ubiquinone AntagonistsBiochemical and Biophysical Research Communications, 1993
- The NADH:ubiquinone oxidoreductase (complex I) of respiratory chainsQuarterly Reviews of Biophysics, 1992
- DISEASES OF THE MITOCHONDRIAL DNAAnnual Review of Biochemistry, 1992
- The respiratory‐chain NADH dehydrogenase (complex I) of mitochondriaEuropean Journal of Biochemistry, 1991
- The effect of ring substituents on the mechanism of interaction of exogenous quinones with the mitochondrial respiratory chainBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1986
- Kinetics of ubiquinol-1-cytochrome c reductase in bovine heart mitochondria and submitochondrial particlesBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1982
- NADH-ubiquinone oxidoreductaseBiochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics, 1976
- Protonmotive redox mechanism of the cytochrome b‐c1 complex in the respiratory chain: Protonmotive ubiquinone cycleFEBS Letters, 1975
- Low molecular weight analogs of coenzyme Q as hydrogen acceptors and donors in systems of the respiratory chainBiochemical and Biophysical Research Communications, 1975
- Four quinone reduction sites in the NADH dehydrogenase complexBiochemical and Biophysical Research Communications, 1970