Lipid packing frustration in the outer leaflet of the plasma membrane prevents scission of caveolae
Lipid packing is a fundamental characteristic of bilayer membranes. It affects all membrane-associated processes ranging from curvature generation to membrane fission. Yet, we lack detailed mechanistic understanding of how lipid packing directly affects these processes in cellular membranes. Here, we address this by focusing on caveolae, small 0-shaped invaginations of the plasma membrane which serve as key regulators of cellular lipid sorting and mechano-responses. In addition to caveolae coat proteins, the lipid membrane is a core component of caveolae that critically impacts both the biogenesis, morphology and stability of such membrane invaginations. We show that the small compound Dyngo-4a adsorbs and inserts into the membrane, resulting in a dramatic dynamin-independent inhibition of caveola dynamics. Analysis of model membranes in combination with molecular dynamics simulations revealed that a substantial amount of Dyngo-4a was inserted and positioned at the level of cholesterol in the bilayer affecting lipid order in a cholesterol dependent manner. Dyngo-4a-treatment resulted in decreased lipid packing of the plasma membrane. This prevented caveolae internalization and lateral diffusion without affecting their morphology, associated proteins, or the overall cell stiffness. Artificially increasing plasma membrane cholesterol levels was found to counteract the block in caveola dynamics caused by Dyngo-4a-mediated lipid packing frustration. Therefore, we propose that the outer leaflet lipid packing of cholesterol in the the plasma membrane critically contributes to the confinement of caveolae to the plasma membrane. Significance statementLarsson et al., demonstrate that lipid packing critically impacts the stability of small 0-shaped plasma membrane cavities termed caveolae. The plasma membrane (PM) release of caveolae is dynamin independent and halted by PM incorporation of the small compound Dyngo-4a, which leads to decreased lipid packing as characterized by the authors. The block in caveola internalization can be counteracted by increased PM levels of cholesterol which is enriched in caveolae and increases the lipid packing. This proof-of-principle study shows that lipid packing controls membrane budding generating membrane vesicles that remain stably associated with the membrane for an extended period of time.