New Insights into the Opening of the Occluded Ligand-Binding Pocket of Sigma1 Receptor: Binding of a Novel Bivalent RC-33 Derivative

Rossino G.; Orellana I.; Caballero J.; Schepmann D.; Wünsch B.; Rui M.; Rossi D.; González-Avendaño M.; Collina, S; Vergara-Jaque A.

Abstract

Significant progresses have been made to understand the molecular basis of the Sigmal receptor (S1R) operating in normal and pathological conditions. S1R is a transmembrane protein that participates in a wide variety of processes at the central nervous system; hence, its function has been associated with mental and neurological disorders. Several ligands have been proposed to regulate the function of S1R revealing a high plasticity of the ligand-binding pocket. Previous drug-design studies have been mainly based on pharmacophore models; however, the recently revealed crystal structure of S1R provides an excellent opportunity for verifying previous predictions and for evaluating the binding of novel compounds. Interestingly, the crystal structure shows that the binding pocket of S1R is highly occluded from solvent; therefore, it is not clear how ligands access this site. In the present work, we applied steered molecular dynamics (SMD) simulations to open the occluded ligand-binding pocket in the S1R crystal structure and to determine the preferred ligand pathway to enter and exit the binding site. The intracellular surface of the beta-barrel ligand-binding region was found the most favorable route to accommodate ligands. This route supports the binding of RC-33 (our in-house-developed S1R modulator) and a new bivalent derivative that constitutes the first divalent structure shown to interact with SIR Free energy calculations of these compounds associated with S1R agree with experimental K-i values and provide molecular insights of the binding mode of modulators that could access the S1R ligand-binding pocket through the cytoplasmic region.

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Título según WOS: New Insights into the Opening of the Occluded Ligand-Binding Pocket of Sigma1 Receptor: Binding of a Novel Bivalent RC-33 Derivative
Título según SCOPUS: New Insights into the Opening of the Occluded Ligand-Binding Pocket of Sigma1 Receptor: Binding of a Novel Bivalent RC-33 Derivative
Título de la Revista: Journal of Chemical Information and Modeling
Volumen: 60
Número: 2
Editorial: AMER CHEMICAL SOC
Fecha de publicación: 2020
Página de inicio: 756
Página final: 765
Idioma: English
DOI:

10.1021/acs.jcim.9b00649

Notas: ISI, SCOPUS