Determination of the Membrane Environment of CD59 in Living Cells

被引:7
作者
Fueloep, Gergo [1 ]
Brameshuber, Mario [1 ]
Arnold, Andreas M. [1 ]
Schuetz, Gerhard J. [1 ]
Sevcsik, Eva [1 ]
机构
[1] TU Wien, Inst Appl Phys, Wiedner Hauptstr 8-10, A-1040 Vienna, Austria
基金
奥地利科学基金会;
关键词
plasma membrane; CD59; lipid; diffusion; micropatterning; GPI-anchored protein; membrane rafts; COMPLEMENT REGULATORY PROTEIN; LIPID-ANCHORED PROTEINS; PLASMA-MEMBRANE; T-LYMPHOCYTES; RAFTS; TRACKING; DIFFUSION; MODEL; CHOLESTEROL; MICROSCOPY;
D O I
10.3390/biom8020028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The organization and dynamics of proteins and lipids in the plasma membrane, and their role in membrane functionality, have been subject of a long-lasting debate. Specifically, it is unclear to what extent membrane proteins are affected by their immediate lipid environment and vice versa. Studies on model membranes and plasma membrane vesicles indicated preferences of proteins for lipid phases characterized by different acyl chain order; however, whether such phases do indeed exist in live cells is still not known. Here, we refine a previously developed micropatterning approach combined with single molecule tracking to quantify the influence of the glycosylphosphatidylinositol-anchored (GPI-anchored) protein CD59 on its molecular environment directly in the live cell plasma membrane. We find that locally enriched and immobilized CD59 presents obstacles to the diffusion of fluorescently labeled lipids with a different phase-partitioning behavior independent of cell cholesterol levels and type of lipid. Our results give no evidence for either specific binding of the lipids to CD59 or the existence of nanoscopic ordered membrane regions associated with CD59.
引用
收藏
页数:13
相关论文
共 45 条
[1]   Monte Carlo simulations of protein micropatterning in biomembranes: effects of immobile sticky obstacles [J].
Arnold, Andreas M. ;
Sevcsik, Eva ;
Schuetz, Gerhard J. .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2016, 49 (36)
[2]   Fluorescence correlation spectroscopy relates rafts in model and native membranes [J].
Bacia, K ;
Scherfeld, D ;
Kahya, N ;
Schwille, P .
BIOPHYSICAL JOURNAL, 2004, 87 (02) :1034-1043
[3]   Flory theory for polymers [J].
Bhattacharjee, Somendra M. ;
Giacometti, Achille ;
Maritan, Amos .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2013, 25 (50)
[4]   Imaging of Mobile Long-lived Nanoplatforms in the Live Cell Plasma Membrane [J].
Brameshuber, Mario ;
Weghuber, Julian ;
Ruprecht, Verena ;
Gombos, Imre ;
Horvath, Ibolya ;
Vigh, Laszlo ;
Eckerstorfer, Paul ;
Kiss, Endre ;
Stockinger, Hannes ;
Schuetz, Gerhard J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (53) :41765-41771
[5]   Diffusion dynamics of glycine receptors revealed by single-quantum dot tracking [J].
Dahan, M ;
Lévi, S ;
Luccardini, C ;
Rostaing, P ;
Riveau, B ;
Triller, A .
SCIENCE, 2003, 302 (5644) :442-445
[6]   Comment to the article by Michael J.!Saxton:: A biological interpretation of transient anomalous subdiffusion.: I.: Qualitative model [J].
Destainville, Nicolas ;
Sauliere, Aude ;
Salome, Laurence .
BIOPHYSICAL JOURNAL, 2008, 95 (07) :3117-3119
[7]   Relationship of lipid rafts to transient confinement zones detected by single particle tracking [J].
Dietrich, C ;
Yang, B ;
Fujiwara, T ;
Kusumi, A ;
Jacobson, K .
BIOPHYSICAL JOURNAL, 2002, 82 (01) :274-284
[8]   Accurate detection and complete tracking of large populations of features in three dimensions [J].
Gao, Yongxiang ;
Kilfoil, Maria L. .
OPTICS EXPRESS, 2009, 17 (06) :4685-4704
[9]   Visualizing lipid structure and raft domains in living cells with two-photon microscopy [J].
Gaus, K ;
Gratton, E ;
Kable, EPW ;
Jones, AS ;
Gelissen, I ;
Kritharides, L ;
Jessup, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (26) :15554-15559
[10]   Lipid raft proteins have a random distribution during localized activation of the T-cell receptor [J].
Glebov, OO ;
Nichols, BJ .
NATURE CELL BIOLOGY, 2004, 6 (03) :238-243