Isolation and characterization of a novel bradykinin potentiating peptide (BPP) from the skin secretion of Phyllomedusa hypochondrialis

Peptides. 2007 Mar;28(3):515-23. doi: 10.1016/j.peptides.2006.10.002. Epub 2006 Nov 13.

Abstract

Bradykinin potentiating peptides (BPPs) from Bothrops jararaca venom were first described in the middle of 1960s and were the first natural inhibitors of the angiotensin-converting enzyme (ACE). BPPs present a classical motif and can be recognized by their typical pyroglutamyl (Pyr)/proline rich sequences presenting, invariably, a proline residue at the C-terminus. In the present study, we describe the isolation and biological characterization of a novel BPP isolated from the skin secretion of the Brazilian tree-frog Phyllomedusa hypochondrialis. This new BPP, named Phypo Xa presents the sequence Pyr-Phe-Arg-Pro-Ser-Tyr-Gln-Ile-Pro-Pro and is able to potentiate bradykinin activities in vivo and in vitro, as well as efficiently and competitively inhibit ACE. This is the first canonical BPP (i.e. Pyr-Aaa(n)-Gln-Ile-Pro-Pro) to be found not only in the frog skin but also in any other natural source other than the snake venoms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Angiotensin-Converting Enzyme Inhibitors / isolation & purification
  • Angiotensin-Converting Enzyme Inhibitors / metabolism
  • Angiotensin-Converting Enzyme Inhibitors / pharmacology
  • Animals
  • Anura / genetics
  • Anura / metabolism*
  • Blood Pressure / drug effects
  • Bradykinin / metabolism*
  • Bradykinin / pharmacology
  • Drug Synergism
  • Female
  • Guinea Pigs
  • Ileum / drug effects
  • In Vitro Techniques
  • Male
  • Oligopeptides / genetics
  • Oligopeptides / isolation & purification*
  • Oligopeptides / metabolism
  • Oligopeptides / pharmacology
  • Rats
  • Rats, Wistar
  • Skin / metabolism

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Oligopeptides
  • bradykinin potentiating factors
  • Bradykinin