| Literature DB >> 12860205 |
Biao-Xin Chai1, Richard R Neubig, Glenn L Millhauser, Darren A Thompson, Pilgrim J Jackson, Gregory S Barsh, Chris J Dickinson, Ji-Yao Li, Yu-Mei Lai, Ira Gantz.
Abstract
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 125I-AgRP (86-132) versus radiolabeled agonist 125I-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.Entities:
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Year: 2003 PMID: 12860205 DOI: 10.1016/s0196-9781(03)00104-9
Source DB: PubMed Journal: Peptides ISSN: 0196-9781 Impact factor: 3.750