Molecular and Cellular Biology · 2012 · 65 citations · 29 references
Life SciencesBiochemistryMolecular BiologyEnzymologyMetabolismStructural BiologyLipid MetabolismMitochondrial BiochemistryMitochondrial BioenergeticsMitochondrial MetabolismMitochondrial PhysiologyStructural EnzymologyCardiolipin RemodelingCardiolipin StructureEnzymesFatty Acyl-coa ThioestersMitochondrial Beta-oxidationMitochondrial EnzymologyMitochondrial Lipid MetabolismThioesterase Activity
Acyl coenzyme A (acyl-CoA) thioesterases hydrolyze thioester bonds in acyl-CoA metabolites. The majority of mammalian thioesterases are α/β-hydrolases and have been studied extensively. A second class of Hotdog-fold enzymes has been less well described. Here, we present a structural and functional analysis of a new mammalian mitochondrial thioesterase, Them5. Them5 and its paralog, Them4, adopt the classical Hotdog-fold structure and form homodimers in crystals. In vitro, Them5 shows strong thioesterase activity with long-chain acyl-CoAs. Loss of Them5 specifically alters the remodeling process of the mitochondrial phospholipid cardiolipin. Them5(-/-) mice show deregulation of lipid metabolism and the development of fatty liver, exacerbated by a high-fat diet. Consequently, mitochondrial morphology is affected, and functions such as respiration and β-oxidation are impaired. The novel mitochondrial acyl-CoA thioesterase Them5 has a critical and specific role in the cardiolipin remodeling process, connecting it to the development of fatty liver and related conditions.
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A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology
David J. Pagliarini, Sarah E. Calvo, Betty Chang et al. · Cell · 2008 · 2K citations · Full text