GPI-anchored proteins do not reside in ordered domains in the live cell plasma membrane

• Published in: Nature communications Vol. 6; no. 1; p. 6969
• Main Authors: Sevcsik, Eva, Brameshuber, Mario, Fölser, Martin, Weghuber, Julian, Honigmann, Alf, Schütz, Gerhard J.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 21.04.2015; Nature Publishing Group
• Subjects: 14/34; 14/35; 14/63; 631/57/2265; 631/57/2271; Carcinoma - metabolism; CD59 Antigens - chemistry; CD59 Antigens - metabolism; Cell Line, Tumor; Cell Membrane - metabolism; Domains; Glycosylphosphatidylinositol; Glycosylphosphatidylinositols - chemistry; Glycosylphosphatidylinositols - metabolism; Green Fluorescent Proteins; Humanities and Social Sciences; Humans; Immunoglobulin Fab Fragments; Lipid rafts; Lipid-Linked Proteins - chemistry; Lipid-Linked Proteins - metabolism; Lipids; Membranes; Micropatterning; multidisciplinary; Plasma; Protein interaction; Protein Structure, Tertiary; Proteins; Rafts; Science; Science (multidisciplinary)
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/ncomms7969

The organization of proteins and lipids in the plasma membrane has been the subject of a long-lasting debate. Membrane rafts of higher lipid chain order were proposed to mediate protein interactions, but have thus far not been directly observed. Here we use protein micropatterning combined with single-molecule tracking to put current models to the test: we rearranged lipid-anchored raft proteins (glycosylphosphatidylinositol(GPI)-anchored-mGFP) directly in the live cell plasma membrane and measured the effect on the local membrane environment. Intriguingly, this treatment does neither nucleate the formation of an ordered membrane phase nor result in any enrichment of nanoscopic-ordered domains within the micropatterned regions. In contrast, we find that immobilized mGFP-GPIs behave as inert obstacles to the diffusion of other membrane constituents without influencing their membrane environment over distances beyond their physical size. Our results indicate that phase partitioning is not a fundamental element of protein organization in the plasma membrane. The existence of membrane rafts of higher lipid order in living cells is subject to ongoing debate. Here, Sevcsik et al . use a micropatterning approach to show that glycosylphosphatidylinositol-anchored proteins, typical raft constituents, do not influence their membrane nanoenvironment to promote raft phase formation.