Interaction between cytochrome P450 2B1 and cytochrome bs: inhibition by synthetic peptides indicates a role for P450 residues Lys-122 and Arg-125

Biochem Biophys Res Commun. 1994 Jun 30;201(3):1090-5. doi: 10.1006/bbrc.1994.1817.

Abstract

Binding of cytochrome b5 to rat cytochrome P450 2B1 was inhibited (by 75%) by a synthetic peptide corresponding to P450 residues 116-134. The role of Lys-122 and Arg-125 were evaluated using peptides in which one or both of these basic residues were replaced with Glu. The Lys-122 substitution nearly abolished while the Arg-125 replacement decreased (by 20%) the inhibitory potential of the peptide. Substitution of both residues resulted in a peptide with no inhibitory activity. These results thus indicate a role for a specific P450 region as well as two basic residues within this region in the cytochrome P450-cytochrome b5 interaction.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Arginine / chemistry
  • Aryl Hydrocarbon Hydroxylases*
  • Cytochrome P-450 Enzyme System / chemistry
  • Cytochrome P-450 Enzyme System / metabolism*
  • Cytochromes b5 / metabolism*
  • Lysine / chemistry
  • Male
  • Microsomes, Liver / metabolism
  • Molecular Sequence Data
  • Peptides / chemistry
  • Protein Binding
  • Rats
  • Rats, Sprague-Dawley
  • Steroid Hydroxylases / chemistry
  • Steroid Hydroxylases / metabolism*

Substances

  • Peptides
  • Cytochromes b5
  • Cytochrome P-450 Enzyme System
  • Arginine
  • Steroid Hydroxylases
  • Aryl Hydrocarbon Hydroxylases
  • steroid 16-beta-hydroxylase
  • Lysine