Variant cDNA sequences of human ATP:citrate lyase: cloning, expression, and purification from baculovirus-infected insect cells

Protein Expr Purif. 1997 Feb;9(1):133-41. doi: 10.1006/prep.1996.0668.

Abstract

ATP:citrate lyase (ACL) is a major generator of cytosolic acetyl-coenzymeA, which is required for both fatty acid and cholesterol biosynthesis. The human ACL (hACL) cDNA was cloned by RT-PCR, and our results indicate the existence of previously unknown sequence variations in hACL. Expression of the hACL cDNA in Spodoptera frugiperda 9 insect cells resulted in the production of high levels of soluble, active enzyme. The recombinant protein (re-hACL) was purified to homogeneity from the soluble lysate of infected cells and was observed to exist as a tetramer by gel filtration chromatography. Kinetic analyses indicated that the re-hACL and rat ACL have very similar enzymological properties. The facile preparation of milligram quantities of purified, active re-hACL affords the opportunity to characterize the enzyme for structure-based design of hypolipidemic drugs, and to further examine the functional significance of the sequence variations.

Publication types

  • Comparative Study

MeSH terms

  • ATP Citrate (pro-S)-Lyase / biosynthesis
  • ATP Citrate (pro-S)-Lyase / genetics*
  • ATP Citrate (pro-S)-Lyase / isolation & purification*
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cloning, Molecular
  • DNA, Complementary / genetics*
  • Gene Expression
  • Genetic Variation*
  • Genetic Vectors
  • Humans
  • Kinetics
  • Molecular Sequence Data
  • Nucleopolyhedroviruses / genetics
  • Polymerase Chain Reaction
  • Rats
  • Recombinant Proteins / biosynthesis
  • Species Specificity
  • Spodoptera / cytology
  • Spodoptera / virology

Substances

  • DNA, Complementary
  • Recombinant Proteins
  • ATP Citrate (pro-S)-Lyase