Unique Interaction Pattern for a Functionally Biased Ghrelin Receptor Agonist

作者：Sivertsen Bjorn; Lang Manja; Frimurer Thomas M; Holliday Nicholas D; Bach Anders; Els Sylvia; Engelstoft Maja S; Petersen Pia S; Madsen Andreas N; Schwartz Thue W; Beck Sickinger Annette G; Holst Birgitte^*

来源：JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286(23): 20845-20860.

DOI：10.1074/jbc.M110.173237

Based on the conformationally constrained D-Trp-Phe-D-Trp (wFw) core of the prototype inverse agonist [D-Arg(1), D-Phe(5), D-Trp(7,9), Leu(11)] substance P, a series of novel, small, peptide-mimetic agonists for the ghrelin receptor were generated. By using various simple, ring-constrained spacers connecting the D-Trp-Phe-D-Trp motif with the important C-terminal carboxyamide group, 40 nM agonism potency was obtained and also in one case (wFw-Isn-NH(2), where Isn is isonipecotic acid) similar to 80% efficacy. However, in contrast to all previously reported ghrelin receptor agonists, the piperidine-constrained wFw-Isn-NH(2) was found to be a functionally biased agonist. Thus, wFw-Isn-NH(2) mediated potent and efficacious signaling through the G alpha(q) and ERK1/2 signaling pathways, but in contrast to all previous ghrelin receptor agonists it did not signal through the serum response element, conceivably the G alpha(12/13) pathway. The recognition pattern of wFw-Isn-NH(2) with the ghrelin receptor also differed significantly from that of all previously characterized unbiased agonists. Most importantly, wFw-Isn-NH(2) was not dependent on GluIII:09 (Glu3.33), which otherwise is an obligatory TM III anchor point residue for ghrelin agonists. Molecular modeling and docking experiments indicated that wFw-Isn-NH(2) binds in the classical agonist binding site between the extracellular segments of TMs III, VI, and VII, interacting closely with the aromatic cluster between TMs VI and VII, but that it does so in an opposite orientation as compared with, for example, the wFw peptide agonists. It is concluded that the novel peptide-mimetic ligand wFw-Isn-NH(2) is a biased ghrelin receptor agonist and that the selective signaling pattern presumably is due to its unique receptor recognition pattern lacking interaction with key residues especially in TM III.

• 出版日期2011-6-10