Membrane surface charge is critical for the transient, yet specific recruitment of proteins with polybasic regions to certain organelles. In eukaryotes, the plasma membrane (PM) is the most electronegative compartment of the cell, which specifies its identity. As such, membrane electrostatics is a central parameter in signaling, intracellular trafficking, and polarity. Here, we explore which are the lipids that control membrane electrostatics using plants as a model. We show that phosphatidylinositol-4-phosphate (PI4P), phosphatidic acidic (PA), and phosphatidylserine (PS) are separately required to generate the electrostatic signature of the plant PM. In addition, we reveal the existence of an electrostatic territory that is organized as a gradient along the endocytic pathway and is controlled by PS/PI4P combination. Altogether, we propose that combinatorial lipid composition of the cytosolic leaflet of organelles not only defines the electrostatic territory but also distinguishes different functional compartments within this territory by specifying their varying surface charges.

Institut Jacques Monod CNRS UMR 7592 Université Paris Diderot Sorbonne Paris Cité Paris 75013 France

Institute of Experimental Botany Czech Academy of Sciences 16502 Prague 6 Lysolaje Czech Republic

Laboratoire Reproduction et Développement des Plantes Université de Lyon ENS de Lyon UCB Lyon 1 CNRS INRA Lyon 69342 France

UMR 5200 Membrane Biogenesis Laboratory CNRS University of Bordeaux Bâtiment A3 INRA Bordeaux Aquitaine 71 Avenue Edouard Bourlaux CS 20032 Villenave d'Ornon 33140 France

UMR 5200 Membrane Biogenesis Laboratory CNRS University of Bordeaux Bâtiment A3 INRA Bordeaux Aquitaine 71 Avenue Edouard Bourlaux CS 20032 Villenave d'Ornon 33140 France; Bordeaux Imaging Center UMS 3420 CNRS US4 INSERM University of Bordeaux Bordeaux 33000 France

UMR 5200 Membrane Biogenesis Laboratory CNRS University of Bordeaux Bâtiment A3 INRA Bordeaux Aquitaine 71 Avenue Edouard Bourlaux CS 20032 Villenave d'Ornon 33140 France; Metabolome Lipidome Facility of Bordeaux Functional Genomics Center Villenave d'Ornon France

Citace poskytuje Crossref.org

Exploring lipid-protein interactions in plant membranes

Biomolecular condensation orchestrates clathrin-mediated endocytosis in plants

DIACYLGLYCEROL KINASE 5 participates in flagellin-induced signaling in Arabidopsis

Phosphatidic Acid in Plant Hormonal Signaling: From Target Proteins to Membrane Conformations

A nanodomain-anchored scaffolding complex is required for the function and localization of phosphatidylinositol 4-kinase alpha in plants

Plasma membrane phospholipid signature recruits the plant exocyst complex via the EXO70A1 subunit

Distinct EH domains of the endocytic TPLATE complex confer lipid and protein binding

Molecular architecture of the endocytic TPLATE complex

Redundant and Diversified Roles Among Selected Arabidopsis thaliana EXO70 Paralogs During Biotic Stress Responses

Arabidopsis Flippases Cooperate with ARF GTPase Exchange Factors to Regulate the Trafficking and Polarity of PIN Auxin Transporters

Arabidopsis Trichome Contains Two Plasma Membrane Domains with Different Lipid Compositions Which Attract Distinct EXO70 Subunits