The σ1 receptor is an integral membrane protein that shares no homology with other receptor systems, has no unequivocally identified natural ligands, but appears to play critical roles in a wide variety of cell functions. While the number of reports of the possible functions of the σ1 receptor is increasing, almost no information about the three-dimensional structure of the receptor and/or possible modes of interaction of the σ1 protein with its ligands have been described. Here we performed an in vitro/in silico investigation to analyze the molecular interactions of the σ1 receptor with its prototypical agonist (+)-pentazocine. Accordingly, 23 mutant σ1 isoforms were generated, and their interactions with (+)-pentazocine were determined experimentally. All direct and/or indirect effects exerted by the mutant residues on the receptor-agonist interactions were reproduced and rationalized in silico, thus shining new light on the three-dimensional structure of the σ1 receptor and its ligand binding site.

The Sigma Enigma:In Vitro/in SilicoSite-Directed Mutagenesis Studies Unveil σ1Receptor Ligand Binding / S., Brune; D., Schepmann; K. H., Klempnauer; Marson, Domenico; DAL COL, Valentina; Laurini, Erik; Fermeglia, Maurizio; B., Wünsch; Pricl, Sabrina. - In: BIOCHEMISTRY. - ISSN 0006-2960. - STAMPA. - 53:18(2014), pp. 2993-3003. [10.1021/bi401575g]

The Sigma Enigma:In Vitro/in SilicoSite-Directed Mutagenesis Studies Unveil σ1Receptor Ligand Binding

MARSON, DOMENICO;DAL COL, VALENTINA;LAURINI, ERIK;FERMEGLIA, MAURIZIO;PRICL, SABRINA
2014-01-01

Abstract

The σ1 receptor is an integral membrane protein that shares no homology with other receptor systems, has no unequivocally identified natural ligands, but appears to play critical roles in a wide variety of cell functions. While the number of reports of the possible functions of the σ1 receptor is increasing, almost no information about the three-dimensional structure of the receptor and/or possible modes of interaction of the σ1 protein with its ligands have been described. Here we performed an in vitro/in silico investigation to analyze the molecular interactions of the σ1 receptor with its prototypical agonist (+)-pentazocine. Accordingly, 23 mutant σ1 isoforms were generated, and their interactions with (+)-pentazocine were determined experimentally. All direct and/or indirect effects exerted by the mutant residues on the receptor-agonist interactions were reproduced and rationalized in silico, thus shining new light on the three-dimensional structure of the σ1 receptor and its ligand binding site.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2793724
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