An aromatic region to induce a switch between agonism and inverse agonism at the ghrelin receptor
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An aromatic region to induce a switch between agonism and inverse agonism at the ghrelin receptor. / Els, Sylvia; Schild, Enrico; Petersen, Pia Steen; Kilian, Tom-Marten; Mokrosinski, Jacek; Frimurer, Thomas M; Chollet, Constance; Schwartz, Thue W; Holst, Birgitte; Beck-Sickinger, Annette G.
I: Journal of Medicinal Chemistry, Bind 55, Nr. 17, 13.09.2012, s. 7437-49.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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T1 - An aromatic region to induce a switch between agonism and inverse agonism at the ghrelin receptor
AU - Els, Sylvia
AU - Schild, Enrico
AU - Petersen, Pia Steen
AU - Kilian, Tom-Marten
AU - Mokrosinski, Jacek
AU - Frimurer, Thomas M
AU - Chollet, Constance
AU - Schwartz, Thue W
AU - Holst, Birgitte
AU - Beck-Sickinger, Annette G
PY - 2012/9/13
Y1 - 2012/9/13
N2 - The ghrelin receptor displays a high constitutive activity suggested to be involved in the regulation of appetite and food intake. Here, we have created peptides with small changes in the core binding motif -wFw- of the hexapeptide KwFwLL-NH(2) that can swap the peptide behavior from inverse agonism to agonism, indicating the importance of this sequence. Introduction of β-(3-benzothienyl)-d-alanine (d-Bth), 3,3-diphenyl-d-alanine (d-Dip) and 1-naphthyl-d-alanine (d-1-Nal) at position 2 resulted in highly potent and efficient inverse agonists, whereas the substitution of d-tryptophane at position 4 with 1-naphthyl-d-alanine (d-1-Nal) and 2-naphthyl-d-alanine (d-2-Nal) induces agonism in functional assays. Competitive binding studies showed a high affinity of the inverse agonist K-(d-1-Nal)-FwLL-NH(2) at the ghrelin receptor. Moreover, mutagenesis studies of the receptor revealed key positions for the switch between inverse agonist and agonist response. Hence, only minor changes in the peptide sequence can decide between agonism and inverse agonism and have a major impact on the biological activity.
AB - The ghrelin receptor displays a high constitutive activity suggested to be involved in the regulation of appetite and food intake. Here, we have created peptides with small changes in the core binding motif -wFw- of the hexapeptide KwFwLL-NH(2) that can swap the peptide behavior from inverse agonism to agonism, indicating the importance of this sequence. Introduction of β-(3-benzothienyl)-d-alanine (d-Bth), 3,3-diphenyl-d-alanine (d-Dip) and 1-naphthyl-d-alanine (d-1-Nal) at position 2 resulted in highly potent and efficient inverse agonists, whereas the substitution of d-tryptophane at position 4 with 1-naphthyl-d-alanine (d-1-Nal) and 2-naphthyl-d-alanine (d-2-Nal) induces agonism in functional assays. Competitive binding studies showed a high affinity of the inverse agonist K-(d-1-Nal)-FwLL-NH(2) at the ghrelin receptor. Moreover, mutagenesis studies of the receptor revealed key positions for the switch between inverse agonist and agonist response. Hence, only minor changes in the peptide sequence can decide between agonism and inverse agonism and have a major impact on the biological activity.
KW - Animals
KW - COS Cells
KW - Cercopithecus aethiops
KW - Feeding Behavior
KW - Humans
KW - Models, Molecular
KW - Mutagenesis
KW - Oligopeptides
KW - Rats
KW - Receptors, Ghrelin
U2 - 10.1021/jm300414b
DO - 10.1021/jm300414b
M3 - Journal article
C2 - 22920150
VL - 55
SP - 7437
EP - 7449
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
SN - 0022-2623
IS - 17
ER -
ID: 47525561