Simple, refined fluorometric method for measuring cystyl-amino peptidase activity

Clin Biochem. 1977 Dec;10(6):193-6. doi: 10.1016/s0009-9120(77)92958-7.

Abstract

Cystyl-amino peptidase (EC 3.4.11.3) activity in serum or plasma was measured fluorometrically using L-cystine-di-beta-naphthylamide in the absence and presence of thiol such as mercaptoethanol. In the presence of thiol, L-cystine-di-beta-naphthylamide is converted to L-cysteine-beta-naphthylamide, and the enzyme activity to hydrolyze L-cysteine-beta-naphthylamide can be measured, while in the absence of thiol, the enzyme activity to hydrolyze L-cystine-di-beta-naphthylamide is determined. Thiol added did not affect various aminopeptidase activities. The present method is able to measure the enzyme activity hydrolyzing L-cystine-di-beta-naphthylamide and L-cysteine-beta-naphthylamide simultaneously and separately using only L-cysteine-di-beta-naphthylamide. This method is simple, sensitive and useful in clinical routine work, assessing placental function for the evaluation of the pregnant status.

MeSH terms

  • Amides / metabolism
  • Aminopeptidases / blood*
  • Cystine / analogs & derivatives
  • Cystine / metabolism
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Mercaptoethanol / pharmacology
  • Pregnancy
  • Spectrometry, Fluorescence

Substances

  • Amides
  • cystine-di-beta-naphthylamide
  • Cystine
  • Mercaptoethanol
  • Aminopeptidases