Skip to main navigation Skip to search Skip to main content

Design of new small cyclic melanocortin receptor-binding peptides using molecular modelling: Role of the His residue in the melanocortin peptide core

  • Peteris Prusis
  • , Ruta Muceniece
  • , Ilze Mutule
  • , Felikss Mutulis
  • , Jarl E.S. Wikberg*
  • *Corresponding author for this work
  • Uppsala University

Research output: Contribution to journal › Article › peer-review

22 Citations (Scopus)

Abstract

The conserved core of melanocyte stimulating hormones (MSH), His-Phe-Arg-Trp, was probed by comparing a cyclic pentapeptide containing His-DPhe-Arg-Trp, with three structurally similar cyclic peptides, that lacked the His residue. All three peptides bound to the MC1, MC3, MC4 and MC5 receptors with similar affinities. Molecular modelling indicated that the 3D structure of the DPhe-Arg-Trp of all three peptides were closely similar. The data indicate that the His residue of the small rigid cyclic MSH core peptides does not participate in binding with the melanocortin receptors.

Original languageEnglish
Pages (from-to)137-146
Number of pages10
JournalEuropean Journal of Medicinal Chemistry
Volume36
Issue number2
DOIs
Publication statusPublished - 1 Feb 2001
Externally publishedYes

Keywords

  • Melanocortin receptors
  • Melanocyte stimulating hormone
  • Molecular modelling
  • Radioligand binding

Fingerprint

Dive into the research topics of 'Design of new small cyclic melanocortin receptor-binding peptides using molecular modelling: Role of the His residue in the melanocortin peptide core'. Together they form a unique fingerprint.

Cite this