(R)-3-hydroxybutyrate dehydrogenase: selective phosphatidylcholine binding by the C-terminal domain

Biochemistry. 2000 Oct 3;39(39):11928-38. doi: 10.1021/bi000425y.

Abstract

(R)-3-Hydroxybutyrate dehydrogenase (BDH) is a lipid-requiring mitochondrial enzyme that has a specific requirement of phosphatidylcholine (PC) for function. The C-terminal domain (CTBDH) of human heart BDH (residues 195-297) has now been expressed in Escherichia coli as a chimera with a soluble protein, glutathione S-transferase (GST), yielding GST-CTBDH, a novel fusion protein that has been purified and shown to selectively bind to PC vesicles. Both recombinant human heart BDH (HH-Histag-BDH) and GST-CTBDH (but not GST) form well-defined protein-lipid complexes with either PC or phosphatidylethanolamine (PE)/diphosphatidylglycerol (DPG) vesicles (but not with digalactosyl diglyceride vesicles) as demonstrated by flotation in sucrose gradients. The protein-PC complexes are stable to 0.5 M NaCl, but complexes of either HH-Histag-BDH or GST-CTBDH with PE/DPG vesicles are dissociated by salt treatment. Thrombin cleavage of GST-CTBDH, either before or after reconstitution with PC vesicles, yields CTBDH (12 111 Da by MALDI mass spectrometry) which retains lipid binding without attached GST. The BDH activator, 1-palmitoyl-2-(1-pyrenyl)decanoyl-PC (pyrenyl-PC), at <2.5% of total phospholipid in vesicles, efficiently quenches a fraction (0.36 and 0.47, respectively) of the tryptophan fluorescence of both HH-Histag-BDH and GST-CTBDH with effective Stern-Volmer quenching constants, (K(Q))(eff), of 11 and 9.3 (%)(-)(1), respectively (half-maximal quenching at approximately 0.1% pyrenyl-PC). Maximal quenching by pyrenyl-PC obtains at approximately stoichiometric pyrenyl-PC to protein ratios, reflecting high-affinity interaction of pyrenyl-PC with both HH-Histag-BDH and GST-CTBDH. The analogous pyrenyl-PE effects a similar maximal quenching of tryptophan fluorescence for both proteins but with approximately 15-fold lower (K(Q))(eff) (half-maximal quenching at approximately 1.5% pyrenyl-PE) referable to nonspecific interaction of pyrenyl-PE with HH-Histag-BDH or GST-CTBDH. Thus, the 103-residue CTBDH constitutes a PC-selective lipid binding domain of the PC-requiring BDH.

Publication types

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

MeSH terms

  • Fluorescent Dyes / chemistry
  • Glutathione Transferase / genetics
  • Histidine / genetics
  • Humans
  • Hydrolysis
  • Hydroxybutyrate Dehydrogenase / chemistry*
  • Hydroxybutyrate Dehydrogenase / genetics
  • Lipid Bilayers / chemistry
  • Myocardium / enzymology
  • Peptide Fragments / chemistry*
  • Peptide Fragments / genetics
  • Peptide Fragments / isolation & purification
  • Phosphatidylcholines / chemistry*
  • Phosphatidylcholines / genetics
  • Protein Binding / genetics
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / isolation & purification
  • Spectrometry, Fluorescence
  • Thrombin / chemistry
  • Tryptophan

Substances

  • Fluorescent Dyes
  • Lipid Bilayers
  • Peptide Fragments
  • Phosphatidylcholines
  • Recombinant Fusion Proteins
  • Histidine
  • 1-palmitoyl-2-pyrenedecanoylphosphatidylcholine
  • Tryptophan
  • Hydroxybutyrate Dehydrogenase
  • Glutathione Transferase
  • Thrombin