Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunit

Biochem Biophys Res Commun. 1995 Apr 6;209(1):47-52. doi: 10.1006/bbrc.1995.1468.

Abstract

We have studied the activities of alpha and beta subunit enzymes of the beta-oxidation trifunctional protein complex in a patient who does not process the alpha-subunit. Long-chain 3-ketoacyl-CoA thiolase, the beta-subunit enzyme, was transported into the mitochondrial matrix, where it expressed normal levels of activity, but was not translocated to the membrane. Thus, intact alpha-subunit is required for trifunctional protein membrane translocation, but is not necessary for conferring activity of the beta-subunit.

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency
  • 3-Hydroxyacyl CoA Dehydrogenases / metabolism
  • Acetyl-CoA C-Acyltransferase / metabolism*
  • Cells, Cultured
  • Humans
  • Infant, Newborn
  • Intracellular Membranes / metabolism
  • Lipid Metabolism, Inborn Errors / metabolism
  • Liver / cytology
  • Liver / enzymology
  • Male
  • Mitochondria / metabolism*
  • Mitochondrial Trifunctional Protein
  • Multienzyme Complexes / metabolism*
  • Protein Binding
  • Skin / cytology
  • Skin / metabolism

Substances

  • Multienzyme Complexes
  • 3-Hydroxyacyl CoA Dehydrogenases
  • Acetyl-CoA C-Acyltransferase
  • Mitochondrial Trifunctional Protein