Dehydration triggers anomalous subdiffusion in biomimetic cell membranes

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Abstract

Lipid diffusion plays a central role in shaping the structural organization of cell membranes, maintaining lipid homeostasis, and facilitating cellular transport and signaling. The lateral mobility of phospholipids in membranes depends heavily on their hydration state. Furthermore, the activation energy of diffusion increases in conditions of reduced membrane hydration, suggesting that the underlying diffusion mechanism changes upon dehydration. Using two variants of fluorescence correlation spectroscopy (point FCS and scanning FCS) and two membrane reporters, we demonstrate that mild dehydration of phase-separated biomimetic cell membranes alters the lipid diffusion mechanism, resulting in anomalous subdiffusion rather than free Brownian motion. Importantly, the anomalous diffusion parameter, α, decreases significantly upon the initial reduction of the membrane hydration layer, and the effect is fully reversible upon rehydration. These observations strongly indicate the reversible shift in lipid diffusion mode rather than irreversible membrane damage. We propose that this anomalous subdiffusion is caused by the formation of temporarily immobile lipid pockets in the membrane upon dehydration. These results therefore provide important insights into the mechanism of lipid diffusion in membranes undergoing local and transient dehydration, which is an important intermediate step in various biological processes associated with membrane fusion, such as neurotransmission, fertilization, and viral entry.

Why it matters

Many biochemical processes, such as cell fusion, neurotransmission, viral entry, and fertilization, involve local, transient membrane dehydration. Therefore, understanding lipid behavior under perturbed hydration conditions is crucial. In this study, we found that phosphatidylcholine lipids undergo a striking transition from free diffusion under fully hydrated conditions to anomalous subdiffusion upon dehydration, which reverses upon rehydration. Our findings reveal that changes in membrane hydration affect not only the rate of lipid diffusion but also the nature of the diffusion process itself. These findings provide new mechanistic insight into the relationship between membrane interfacial hydration and nanoscale lipid mobility. More broadly, our study establishes hydration-controlled supported lipid bilayers as a well-defined experimental platform for investigating anomalous and obstructed diffusion in membrane systems.

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