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Enzymology
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- BioenergeticsOpen Access
Oversized ubiquinones as molecular probes for structural dynamics of the ubiquinone reaction site in mitochondrial respiratory complex I
Journal of Biological ChemistryVol. 295Issue 8p2449–2463Published online: January 17, 2020- Shinpei Uno
- Takahiro Masuya
- Kyoko Shinzawa-Itoh
- Jonathan Lasham
- Outi Haapanen
- Tomoo Shiba
- and others
Cited in Scopus: 14NADH-quinone oxidoreductase (complex I) couples electron transfer from NADH to quinone with proton translocation across the membrane. Quinone reduction is a key step for energy transmission from the site of quinone reduction to the remotely located proton-pumping machinery of the enzyme. Although structural biology studies have proposed the existence of a long and narrow quinone-access channel, the physiological relevance of this channel remains debatable. We investigated here whether complex I in bovine heart submitochondrial particles (SMPs) can catalytically reduce a series of oversized ubiquinones (OS-UQs), which are highly unlikely to transit the narrow channel because their side chain includes a bulky “block” that is ∼13 Å across.