Abstract
The melanocortin (MC) receptor subtypes have distinctive characteristic binding profiles. We found that the trout and Fugu MC4 receptors have similar affinity for α-MSH and β-MSH and a much higher affinity for ACTH than does the human MC4 receptor. The Fugu MC1 and the trout and Fugu MC5 receptors also have higher affinity for ACTH-derived peptides than α-, β-, or γ-MSH. It is tempting to speculate that ACTH-derived peptides may have played an important role as "original" ligands at the MC receptors, while the specificity of the different subtypes for the α-, β-, and γ-MSH peptides may have appeared at later stages during vertebrate evolution.
| Original language | English |
|---|---|
| Pages (from-to) | 337-339 |
| Number of pages | 3 |
| Journal | Annals of the New York Academy of Sciences |
| Volume | 1040 |
| DOIs | |
| Publication status | Published - 2005 |
Keywords
- ACTH
- Evolution
- GPCR
- Melanocortin
- MSH
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