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 language | English |
|---|---|
| Pages (from-to) | 137-146 |
| Number of pages | 10 |
| Journal | European Journal of Medicinal Chemistry |
| Volume | 36 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 1 Feb 2001 |
| Externally published | Yes |
Keywords
- Melanocortin receptors
- Melanocyte stimulating hormone
- Molecular modelling
- Radioligand binding
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