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DOE OSTI · 2549461

Highly tail-asymmetric lipids interdigitate and cause bidirectional ordering

Abstract

Phospholipids form structurally and compositionally diverse membranes. A less studied type of compositional diversity involves phospholipid tail variety. Some phospholipids contain two acyl tails which differ in length. These tail-asymmetric lipids are shown to contribute to temperature sensitivity, oxygen adaptability, and membrane fluidity. Membranes of a highly virulent intracellular bacterium, Francisella tularensis, contain highly tail-asymmetric 1-lignoceroyl-2-decanoyl-sn-glycero-3-phosphatidylethanolamine (XJPE) lipids which were previously shown to inhibit inflammatory responses in host cells. XJPE tails have unusually high asymmetry, and how they contribute to membrane properties on a molecular level is unknown. Here, we use small angle X-ray scattering and molecular dynamics simulations to investigate how varying XJPE ratios alters properties of simple membranes. Our results demonstrate that at high concentration they promote liquid-to-gel transition in otherwise liquid membranes, while at low concentration they are tolerated well, minimally altering membrane properties. In liquid membranes, XJPE lipids dynamically adopt two main conformations; with the long tail extended into the opposing leaflet or bent-back residing in its own leaflet. When added to both leaflets XJPE primarily adopts an extended confirmation, while asymmetric addition results in more bent-back orientations. The former increases tail ordering and the latter decreases it. XJPE tails adopt different conformations that induce composition- and leaflet-dependent bidirectional effect on membrane fluidity and this suggests that Francisella tularensis could use tail asymmetry to facilitate vesicle fusion and destabilize host cells. The effect of tail-asymmetric lipids on complex membranes should be further investigated to reveal the regulatory roles of high tail asymmetry.

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BibTeXRIS

Ozturk, Tugba N. [Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)] (ORCID:0000000172259546), Ferron, Thomas J. [Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)] (ORCID:0000000222422648), He, Wei [Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)], Schwarz, Benjamin [National Institutes of Health (NIH), Hamilton, MT (United States)], Weiss, Thomas M. [SLAC National Accelerator Laboratory (SLAC), Menlo Park, CA (United States). Stanford Synchrotron Radiation Lightsource (SSRL)], Fischer, Nicholas O. [Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)] (ORCID:0000000175754390), Rasley, Amy [Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)], Carpenter, Timothy S. [Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)], Bosio, Catharine M. [National Institutes of Health (NIH), Hamilton, MT (United States)], Ingólfsson, Helgi I. [Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)] (ORCID:0000000276139143). 2025-04-04. Highly tail-asymmetric lipids interdigitate and cause bidirectional ordering. https://doi.org/10.1016/j.jlr.2025.100797

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