Synthesis and biological evaluation of α-MSH analogues substituted with alanine

Ulrike G. Sahm, George W J Olivier, Sarah K. Branch, Stephen H. Moss, Colin W. Pouton

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Abstract

The influence of single amino acid replacements by alanine on the binding affinity and biological activity of α-MSH in B16 murine melanoma cells has been studied systematically. α-MSH analogues were synthesized by solid-phase peptide synthesis and their binding affinities to the melanocortin receptor expressed by B16 mouse melanoma cells were determined using a radioreceptor assay. Biological activity of the analogues was determined by measuring tyrosinase stimulation. Relative activity and affinity data were generally in agreement with earlier results using terminal deletion fragments of α-MSH, but the alanine scan revealed important new insights into the role of individual residues. The three terminal amino acids at either end were not necessary for binding or activity, with amino acids 4-9 forming a core sequence required for receptor binding and triggering of the biological response. It was observed that replacement of the glutamic acid residue in position 5 was possible without loss of affinity or activity, whereas replacement of Met4 resulted in a 100-fold loss of binding affinity and biological activity. Each residue within the conserved melanocortin sequence His-Phe-Arg-Trp was shown to be essential with Phe7, Arg8, and Trp9 being the most sensitive to replacement by alanine. Generally, there was a rank correlation between binding affinity and tyrosinase stimulation within the group of analogues studied. Tyrosinase activity was less affected by alanine substitution than binding affinity, which suggests that full receptor binding is not required for maximum biological response.

Original languageEnglish
Pages (from-to)1297-1302
Number of pages6
JournalPeptides
Volume15
Issue number7
DOIs
Publication statusPublished - 1 Jan 1994

Keywords

  • Alanine substitution
  • B16 murine melanoma cells
  • Binding affinity
  • Structure-activity relationships
  • Tyrosinase activity
  • α-Melanocyte-stimulating hormone

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