A novel branched-chain amino acid metabolon: Protein-protein interactions in a supramolecular complex

Mohammad Mainul Islam, Reidar Wallin, R. Max Wynn, Myra Conway, Hisao Fujii, James A. Mobley, David T. Chuang, Susan M. Hutson

Research output: Contribution to journalArticle

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Abstract

The catabolic pathways of branched-chain amino acids have two common steps. The first step is deamination catalyzed by the vitamin B6-dependent branched-chain aminotransferase isozymes (BCATs) to produce branched-chain α-keto acids (BCKAs). The second step is oxidative decarboxylation of the BCKAs mediated by the branched-chain α-keto acid dehydrogenase enzyme complex (BCKD complex). The BCKD complex is organized around a cubic core consisting of 24 lipoate-bearing dihydrolipoyl transacylase (E2) subunits, associated with the branched-chain α-keto acid decarboxylase/dehydrogenase (E1), dihydrolipoamide dehydrogenase (E3), BCKD kinase, and BCKD phosphatase. In this study, we provide evidence that human mitochondrial BCAT (hBCATm) associates with the E1 decarboxylase component of the rat or human BCKD complex with a KD of 2.8 μM. NADH dissociates the complex. The E2 and E3 components do not interact with hBCATm. In the presence of hBCATm, k cat values for E1-catalyzed decarboxylation of the BCKAs are enhanced 12-fold. Mutations of hBCATm proteins in the catalytically important CXXC center or E1 proteins in the phosphorylation loop residues prevent complex formation, indicating that these regions are important for the interaction between hBCATm and E1. Our results provide evidence for substrate channeling between hBCATm and BCKD complex and formation of a metabolic unit (termed branched-chain amino acid metabolon) that can be influenced by the redox state in mitochondria.

Original languageEnglish (US)
Pages (from-to)11893-11903
Number of pages11
JournalJournal of Biological Chemistry
Volume282
Issue number16
DOIs
StatePublished - Apr 20 2007

Fingerprint

3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Keto Acids
Branched Chain Amino Acids
Carboxy-Lyases
Enzymes
Decarboxylation
Isoenzymes
Proteins
Bearings (structural)
Dihydrolipoamide Dehydrogenase
Phosphorylation
Mitochondria
Vitamin B 6
Deamination
Phosphoric Monoester Hydrolases
NAD
Rats
Oxidoreductases
Phosphotransferases
Oxidation-Reduction

ASJC Scopus subject areas

  • Biochemistry

Cite this

A novel branched-chain amino acid metabolon : Protein-protein interactions in a supramolecular complex. / Islam, Mohammad Mainul; Wallin, Reidar; Wynn, R. Max; Conway, Myra; Fujii, Hisao; Mobley, James A.; Chuang, David T.; Hutson, Susan M.

In: Journal of Biological Chemistry, Vol. 282, No. 16, 20.04.2007, p. 11893-11903.

Research output: Contribution to journalArticle

Islam, Mohammad Mainul ; Wallin, Reidar ; Wynn, R. Max ; Conway, Myra ; Fujii, Hisao ; Mobley, James A. ; Chuang, David T. ; Hutson, Susan M. / A novel branched-chain amino acid metabolon : Protein-protein interactions in a supramolecular complex. In: Journal of Biological Chemistry. 2007 ; Vol. 282, No. 16. pp. 11893-11903.
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