Isolation of a cDNA clone for the dihydrolipoamide acetyltransferase component of the human liver pyruvate dehydrogenase complex

Biochem Biophys Res Commun. 1987 Jun 15;145(2):903-7. doi: 10.1016/0006-291x(87)91050-3.

Abstract

Dihydrolipoamide acetyltransferase (E2) forms the structural core of pyruvate dehydrogenase complex. A cDNA clone (lambda E2-1) for mammalian E2 was identified from a human liver lambda gt11 library using anti-E2 serum. Affinity-selected antibodies using the fusion protein from lambda E2-1 immuno-reacted specifically with E2 of purified pyruvate dehydrogenase complex on immuno-blot analysis. The cDNA insert was approximately 2.3 kb in length with an internal EcoR1 site generating 1.4 and 0.9 kb fragments. A synthetic 17-mer oligodeoxynucleotide mixture based on the amino acid sequence surrounding the lipoic acid-containing lysine residue in bovine kidney E2 hybridized with the 2.3 kb cDNA insert and the 1.4 kb fragment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetyltransferases / genetics*
  • Amino Acid Sequence
  • Cloning, Molecular
  • DNA / isolation & purification*
  • DNA Restriction Enzymes / metabolism
  • Deoxyribonuclease EcoRI
  • Dihydrolipoyllysine-Residue Acetyltransferase
  • Humans
  • Immunosorbent Techniques
  • Mitochondria, Liver / enzymology
  • Pyruvate Dehydrogenase Complex / analysis*

Substances

  • Pyruvate Dehydrogenase Complex
  • DNA
  • Acetyltransferases
  • Dihydrolipoyllysine-Residue Acetyltransferase
  • DNA Restriction Enzymes
  • Deoxyribonuclease EcoRI