Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/98895
Author(s): Armenio Moura M Barbosa
Francesca De Rienzo
Maria J Ramos
Maria Cristina Menziani
Title: Computational analysis of ligand recognition sites of homo- and heteropentameric 5-HT3 receptors
Issue Date: 2010
Abstract: Inhibition of the 5-hydroxytryptamine receptor (5-HT3R), a member of the Cys-loop superfamily of Ligand-Gated Ion Channels (LGICs), has been recognized to have important antiemetic effects. With respect to the many other drugs already in use, such as the first generation 5-HT3R antagonist granisetron, palonosetron, a second generation antagonist, clearly demonstrates superior inhibition potency towards the 5-HT(3)Rs. Five different receptor monomers, the 5-HT3R A-E, have been identified although the A and B subunits are the only known to build functional receptors, the homopentameric 5-HT3AR and the heteropentameric 5-HT3B-AR (with BBABA subunit arrangement). At present, however, no three-dimensional structure has been reported for any of the 5-HT3R subunits. To understand the binding properties of agonists and antagonists, models of the extracellular portion of the 5-HT3R A and B subunits are built and assembled into the receptor (homo- and hetero-) pentameric structure on the basis of the known three-dimensional structure of the nicotinic-acetylcholine receptor (nACh-R). The results of docking studies of the natural agonist serotonin and the antagonists palonosetron and granisetron into the modelled homomeric and heteromeric 5-HT3R binding interfaces, provide a possible rationalization both of the higher potency of palonosetron with respect to other antagonists, and of its previously reported allosteric binding and positive cooperativity properties.
Subject: Medicina básica
Basic medicine
Scientific areas: Ciências médicas e da saúde::Medicina básica
Medical and Health sciences::Basic medicine
URI: https://repositorio-aberto.up.pt/handle/10216/98895
Document Type: Artigo em Revista Científica Internacional
Rights: restrictedAccess
Appears in Collections:FCUP - Artigo em Revista Científica Internacional

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