Identification of human placental leucine aminopeptidase as oxytocinase

Arch Biochem Biophys. 1992 Feb 1;292(2):388-92. doi: 10.1016/0003-9861(92)90007-j.

Abstract

Human placental leucine aminopeptidase (P-LAP) was purified from retroplacental serum for the first time by serial chromatography on columns of Matrex Blue A, DEAE-Sepharose CL-6B, phenyl-Sepharose 4B, chelating-Sepharose, and Sepharose CL-6B. The purified P-LAP was apparently homogeneous on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the apparent molecular weight (Mr) was estimated to be 210,000. By comparing P-LAP activity with cystine aminopeptidase activity, we concluded that both activities were shared by the same molecule. We also examined the hydrolytic activity of P-LAP using naturally occurring peptide hormones and found that the enzyme hydrolyzed oxytocin, vasopressin, and angiotensin III. These results suggest that P-LAP shows oxytocinase activity and plays an important role in the regulation of the plasma level of these hormones during pregnancy.

MeSH terms

  • Chromatography, Gel
  • Chromatography, Ion Exchange
  • Cystinyl Aminopeptidase / blood*
  • Cystinyl Aminopeptidase / isolation & purification
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Fetal Blood
  • Humans
  • Kinetics
  • Leucyl Aminopeptidase / blood*
  • Leucyl Aminopeptidase / isolation & purification
  • Molecular Weight
  • Placenta
  • Pregnancy
  • Substrate Specificity

Substances

  • Leucyl Aminopeptidase
  • Cystinyl Aminopeptidase