New insight into active muscarinic receptors with the novel radioagonist [³H]iperoxo.
Biochem Pharmacol
; 90(3): 307-19, 2014 Aug 01.
Article
em En
| MEDLINE
| ID: mdl-24863257
ABSTRACT
Activation of G protein-coupled receptors involves major conformational changes of the receptor protein ranging from the extracellular transmitter binding site to the intracellular G protein binding surface. GPCRs such as the muscarinic acetylcholine receptors are commonly probed with radioantagonists rather than radioagonists due to better physicochemical stability, higher affinity, and indifference towards receptor coupling states of the former. Here we introduce tritiated iperoxo, a superagonist at muscarinic M2 receptors with very high affinity. In membrane suspensions of transfected CHO-cells, [³H]iperoxo - unlike the common radioagonists [³H]acetylcholine and [³H]oxotremorine M - allowed labelling of each of the five muscarinic receptor subtypes in radioagonist displacement and saturation binding studies. [³H]iperoxo revealed considerable differences in affinity between the even- and the odd-numbered muscarinic receptor subtypes with affinities for the M2 and M4 receptor in the picomolar range. Probing ternary complex formation on the M2 receptor, [³H]iperoxo dissociation was not influenced by an archetypal allosteric inverse agonist, reflecting activation-related rearrangement of the extracellular loop region. At the inner side of M2, the preferred Gi protein acted as a positive allosteric modulator of [³H]iperoxo binding, whereas Gs and Gq were neutral in spite of their robust coupling to the activated receptor. In intact CHO-hM2 cells, endogenous guanylnucleotides promoted receptor/G protein-dissociation resulting in low-affinity agonist binding which, nevertheless, was still reported by [³H]iperoxo. Taken together, the muscarinic superagonist [³H]iperoxo is the best tool currently available for direct probing activation-related conformational transitions of muscarinic receptors.
Palavras-chave
Acetylcholine; Allosteric modulation; Atropine; Cholera toxin (CTX); G protein-coupled receptor; Guanosine triphosphate (GTP); Iperoxo; Muscarinic acetylcholine receptor; N-methylscopolamine (NMS); Pertussis toxin (PTX); Pilocarpine; Superagonism; W84 (3-(1,3-dioxoisoindol-2-yl)propyl-[6-[3-(1,3-dioxoisoindol-2-yl)propyl-dimethylazaniumyl]hexyl]-dimethylazanium); [(3)H]iperoxo
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Receptores Muscarínicos
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Agonistas Muscarínicos
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Compostos de Amônio Quaternário
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Isoxazóis
/
Modelos Biológicos
Idioma:
En
Revista:
Biochem Pharmacol
Ano de publicação:
2014
Tipo de documento:
Article
País de afiliação:
Alemanha