Boundary Lipids of the Nicotinic Acetylcholine Receptor in Quasi-Native Membranes

Abstract

The nicotinic acetylcholine receptor (nAChR) is a neurotransmitter receptor and pentameric ligand gated ion channel (pLGIC) critical for signaling across synapses, including the neuromuscular junction. In reconstituted membranes, the nAChR function depends heavily on cholesterol, leading to the hypothesis that nAChR will partition into cholesterol-enriched liquid-ordered domains ("rafts”). Native nAChR membranes are rich in lipids with saturated fatty acid (like palmitic acid) or polyunsaturated fatty acid (PUFA) acyl chains (like docosahexaenoic acid (DHA)). Using coarse-grained molecular dynamics simulations we characterized preferential lipid interactions and partitioning behavior of nAChR in binary membranes (cholesterol and lipids with two palmitic acid acyl chains) ternary membranes (cholesterol, a lipid with two palmitic acid acyl chains, and lipids with either two chains composed of the long-chain omega-3 PUFA DHA or of the omega-6 PUFA linoleic acid). We quantify occupation of non-annular and annular regions by cholesterol and saturated and polyunsaturated lipids. In the absence of PUFAs, cholesterol is enriched in the nAChR annulus in a concentration-dependent manner. Cholesterol is also distributed throughout the non-annular (embedded) sites, while palmatic acyl chains persistently occupy only one interface between the beta and alpha subunits. When lipids containing long-chain PUFA acyl chains are introduced, they displace cholesterol from two additional interfaces. Contrary to expectations, in domain-forming membranes containing PUFAs, the nAChR is observed to consistently partition into PUFA-rich, cholesterol-poor domains. Saturated lipids with either phosphatidylcholine and phosphatidylethanolamine head groups are significantly depleted in such systems, although the extent of depletion is reduced for phosphatidylethanolamine. While nAChR consistently partitions into the cholesterol poor domain, alpha-gamma and delta-beta faces interact more than other faces with the cholesterol-rich domains. We extend this approach to more complex membranes of interest, including more realistic synaptic membranes and the Xenopus oocyte membranes used for electrophysiology.