Inverse agonist activity of agouti and agouti-related protein

Agouti and agouti-related protein (AgRP) are endogenous antagonists of the melanocortin receptors (MCxR). Previous data showed that recombinant full-length agouti and a synthetic fragment of AgRP, AgRP (83–132), are inverse agonists at the MC1R and MC4R, respectively. This study demonstrates the sma...

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Veröffentlicht in:Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2003-04, Vol.24 (4), p.603-609
Hauptverfasser: Chai, Biao-Xin, Neubig, Richard R., Millhauser, Glenn L., Thompson, Darren A., Jackson, Pilgrim J., Barsh, Gregory S., Dickinson, Chris J., Li, Ji-Yao, Lai, Yu-Mei, Gantz, Ira
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Sprache:eng
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Zusammenfassung:Agouti and agouti-related protein (AgRP) are endogenous antagonists of the melanocortin receptors (MCxR). Previous data showed that recombinant full-length agouti and a synthetic fragment of AgRP, AgRP (83–132), are inverse agonists at the MC1R and MC4R, respectively. This study demonstrates the smaller analogs AgRP (87–120) and ASIP [90–132 (L89Y)], and short peptides Yc[CRFFNAFC]Y and Qc[CRFFRSAC]S are also MC4R inverse agonists. Furthermore, the relative affinity of the series of MC4R ligands for displacement of radiolabeled antagonist 125 I -AgRP (86–132) versus radiolabeled agonist 125 I -NDP-MSH did not correlate with ligand efficacy, which is more consistent with an induced-fit model than a simple two-state model of MC4R activation. These data shed new light on the determinants and mechanism of inverse agonism at the MC4R.
ISSN:0196-9781
1873-5169
DOI:10.1016/S0196-9781(03)00104-9