Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel
| العنوان: | Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel |
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| المؤلفون: | Giuseppe Brancato, Danilo Di Maio, Balasubramanian Chandramouli |
| المساهمون: | DI MAIO, Danilo, Chandramouli, Balasubramanian, Brancato, Giuseppe |
| المصدر: | PLoS ONE PLoS ONE, Vol 10, Iss 10, p e0140258 (2015) |
| بيانات النشر: | Public Library of Science (PLoS), 2015. |
| سنة النشر: | 2015 |
| مصطلحات موضوعية: | Models, Molecular, Protein Conformation, lcsh:Medicine, Mice, Protein structure, Animals, Ion, lcsh:Science, Glycine receptor, Ion transporter, Ions, Multidisciplinary, Animal, Chemistry, GABAA receptor, lcsh:R, Biological Transport, Light-gated ion channel, Transmembrane domain, Biochemistry, Mutation, Biophysics, Ligand-gated ion channel, lcsh:Q, Receptors, Serotonin, 5-HT3, Signal transduction, Signal Transduction, Research Article |
| الوصف: | Pentameric ligand gated ion channels (pLGICs) are ionotropic receptors that mediate fast intercellular communications at synaptic level and include either cation selective (e.g., nAChR and 5-HT3) or anion selective (e.g., GlyR, GABAA and GluCl) membrane channels. Among others, 5-HT3 is one of the most studied members, since its first cloning back in 1991, and a large number of studies have successfully pinpointed protein residues critical for its activation and channel gating. In addition, 5-HT3 is also the target of a few pharmacological treatments due to the demonstrated benefits of its modulation in clinical trials. Nonetheless, a detailed molecular analysis of important protein features, such as the origin of its ion selectivity and the rather low conductance as compared to other channel homologues, has been unfeasible until the recent crystallization of the mouse 5-HT3A receptor. Here, we present extended molecular dynamics simulations and free energy calculations of the whole 5-HT3A protein with the aim of better understanding its ion transport properties, such as the pathways for ion permeation into the receptor body and the complex nature of the selectivity filter. Our investigation unravels previously unpredicted structural features of the 5-HT3A receptor, such as the existence of alternative intersubunit pathways for ion translocation at the interface between the extracellular and the transmembrane domains, in addition to the one along the channel main axis. Moreover, our study offers a molecular interpretation of the role played by an arginine triplet located in the intracellular domain on determining the characteristic low conductance of the 5-HT3A receptor, as evidenced in previous experiments. In view of these results, possible implications on other members of the superfamily are suggested. |
| تدمد: | 1932-6203 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f599a9171d0d9fb24a8a06b4b7e01deTest https://doi.org/10.1371/journal.pone.0140258Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....7f599a9171d0d9fb24a8a06b4b7e01de |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 19326203 |
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