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Unusual Robustness of Neurotransmitter Vesicle Membranes against Serotonin-Induced Perturbations

Ankur Gupta, Paweł Krupa, Oskar Engberg, Magdalena A. Krupa, Ankur Chaudhary, Mai Suan Li, Daniel Huster, Sudipta Maiti

2023The Journal of Physical Chemistry B12 citationsDOI

Abstract

Nature confines hundreds of millimolar of amphiphilic neurotransmitters, such as serotonin, in synaptic vesicles. This appears to be a puzzle, as the mechanical properties of lipid bilayer membranes of individual major polar lipid constituents of synaptic vesicles [phosphatidylcholine (PC), phosphatidylethanolamine (PE), and phosphatidylserine (PS)] are significantly affected by serotonin, sometimes even at few millimolar concentrations. These properties are measured by atomic force microscopy, and their results are corroborated by molecular dynamics simulations. Complementary 2 H solid-state NMR measurements also show that the lipid acyl chain order parameters are strongly affected by serotonin. The resolution of the puzzle lies in the remarkably different properties displayed by the mixture of these lipids, at molar ratios mimicking those of natural vesicles (PC:PE:PS:Cholesterol = 3:5:2:5). Bilayers constituting of these lipids are minimally perturbed by serotonin, and show only a graded response at physiological concentrations (>100 mM). Significantly, the cholesterol (up to 33% molar ratio) plays only a minor role in dictating these mechanical perturbations, with PC:PE:PS:Cholesterol = 3:5:2:5 and 3:5:2:0 showing similar perturbations. We infer that nature uses an emergent mechanical property of a specific mixture of lipids, all individually vulnerable to serotonin, to appropriately respond to physiological serotonin levels.

Topics & Concepts

VesiclePhosphatidylethanolaminePhosphatidylcholineSerotoninBiophysicsBilayerNeurotransmitterChemistryPhosphatidylserineMembraneSynaptic vesicleLipid bilayerAmphiphileBiochemistryPhospholipidBiologyOrganic chemistryPolymerReceptorCopolymerLipid Membrane Structure and BehaviorNeuroscience and Neuropharmacology ResearchCellular transport and secretion
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