Year: 2026
Type: article
Abstract: Phosphatidylinositol phosphate (PIP) lipids, enriched on the cytoplasmic leaflet of the plasma membrane, are key regulators of diverse cellular processes, often through interactions with partner proteins that regulate actin assembly. Supported lipid bilayers (SLBs) provide a powerful model system to study the interactions of PIP lipids with their partner proteins. However, despite advances in SLB preparation methods, it remains a challenge to robustly obtain fluid SLBs in which PIP lipids are both mobile and asymmetrically distributed. In this study, we report a simple and robust method to generate asymmetric SLBs containing tunable amounts of PI(4,5)P 2 . By dissolving PI(4,5)P 2 below its critical micelle concentration (CMC), we enable its spontaneous insertion into the upper leaflet of SLBs exposed to bulk solution. The mobility of PI(4,5)P 2 is confirmed using fluorescence recovery after photobleaching (FRAP). Furthermore, we demonstrate that PI(4,5)P 2 incorporated using this method retains its functionality, recruiting binding partners, actin-membrane linker ezrin, and myosin 1 motors capable of sliding actin filaments on the SLBs. Our method offers a straightforward strategy to generate asymmetric PI(4,5)P 2 -containing SLBs and is applicable to other lipid species with high CMC values.
Source: Langmuir
Institutions: Centre National de la Recherche Scientifique, Université Paris Sciences et Lettres, Sorbonne Université, Physique des Cellules et Cancers, Institut Curie, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, Université Paris-Saclay, Institut de Biologie Intégrative de la Cellule, Université Paris Cité, Physique et Mécanique des Milieux Hétérogènes, ESPCI Paris, Yale University, École Normale Supérieure - PSL, Laboratoire de Physique de l'ENS de Lyon, Laboratoire de Physique de l'Ecole Normale Supérieure, Chimie Physique et Chimie du Vivant
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Funders: Infrastructures en Biologie Santé et Agronomie, Agence Nationale de la Recherche, Centre National de la Recherche Scientifique, Université de Recherche Paris Sciences et Lettres, Institut Curie, Labex CelTisPhyBio, National Institute of General Medical Sciences, HORIZON EUROPE Marie Sklodowska-Curie Actions
OpenAlex ID: W7140773308
