An active insect kinin analog with 4-aminopyroglutamate, a novel cis-peptide bond, type VI beta-turn motif

Biopolymers. 2004 Dec 5;75(5):412-9. doi: 10.1002/bip.20155.

Abstract

The insect kinins are potent diuretic peptides that preferentially form a cis-Pro, type VI beta-turn. An insect kinin analog containing (2S,4S)-4-aminopyroglutamate, a novel cis-peptide bond, type VI beta-turn motif, demonstrates significant activity in the physiological range in a cricket diuretic assay. This is the first instance of a 4-aminopyroglutamate analog of a peptide with a preference for a type VI turn that demonstrates significant bioactivity. The results provide further confirmatory evidence for the active conformation of the insect kinins, and a new scaffold with which to design biostable, peptidomimetic analogs capable of disrupting critical insect kinin-regulated processes in insects.

Publication types

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

MeSH terms

  • Animals
  • Diuretics / chemistry
  • Diuretics / pharmacology
  • Gryllidae / drug effects
  • Insect Proteins / chemistry*
  • Insect Proteins / pharmacology
  • Kinins / chemistry*
  • Kinins / pharmacology
  • Magnetic Resonance Spectroscopy
  • Oligopeptides / chemistry*
  • Oligopeptides / pharmacology
  • Protein Structure, Secondary
  • Pyrrolidonecarboxylic Acid / analogs & derivatives*
  • Pyrrolidonecarboxylic Acid / chemistry*

Substances

  • 4-aminopyroglutamate
  • Diuretics
  • Insect Proteins
  • Kinins
  • Oligopeptides
  • Pyrrolidonecarboxylic Acid