Cholesterol Content in the Membrane Promotes Key Lipid-Protein Interactions in a Pentameric Serotonin-Gated Ion Channel

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Pentameric ligand-gated ion channels (pLGICs), embedded in the lipid membranes of nerve cells, mediate fast synaptic transmission and are major pharmaceutical targets. Because of their complexity and the limited knowledge of their structure, their working mechanisms have still to be fully unravelled at the molecular level. Over the past years, evidence that the lipid membrane may modulate the function of membrane proteins, including pLGICs, has emerged.
Here we investigate, by means of molecular dynamics simulations, the behaviour of the lipid membrane at the interface with the 5-HT_3A receptor (5-HT_3AR), a representative pLGIC which is the target of nausea-suppressant drugs, in a non-conductive state. Three lipid compositions are studied, spanning different concentrations of the phospholipids POPC and POPE and of cholesterol, hence a range of viscosities. A variety of lipid interactions and persistent binding events to different parts of the receptor are revealed in the investigated models, providing snapshots of the dynamical environment at the membrane-receptor interface. Some of these events result in lipid intercalation within the transmembrane domain and others reach out to protein key sections for signal transmission and receptor activation, such as the Cys-loop and the M2-M3 loop. In particular, phospholipids, with their long hydrophobic tails, play an important role role in these interactions, potentially providing a bridge between these two structures. A higher cholesterol content appears to promote lipid persistent binding to the receptor.
Original languageEnglish
Article number061018
Issue number6
Publication statusAccepted/In press - 3 Dec 2020


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