Membrane Lipid Nanodomains

被引:150
作者
Cebecauer, Marek [1 ]
Amaro, Mariana [1 ]
Jurkiewicz, Piotr [1 ]
Sarmento, Maria Joao [1 ]
Sachl, Radek [1 ]
Cwiklik, Lukasz [1 ]
Hof, Martin [1 ]
机构
[1] Czech Acad Sci, J Heyrovsky Inst Phys Chem, Dolejskova 3, Prague 18223 8, Czech Republic
关键词
ATOMIC-FORCE MICROSCOPY; FLUORESCENCE CORRELATION SPECTROSCOPY; FATTY-ACID CHAIN; GIANT UNILAMELLAR VESICLES; GPI-ANCHORED PROTEINS; C-KINASE SUBSTRATE; MOLECULAR-DYNAMICS SIMULATIONS; THERMOTROPIC PHASE-BEHAVIOR; CERAMIDE-ENRICHED DOMAINS; RESONANCE ENERGY-TRANSFER;
D O I
10.1021/acs.chemrev.8b00322
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lipid membranes can spontaneously organize their components into domains of different sizes and properties. The organization of membrane lipids into nanodomains might potentially play a role in vital functions of cells and organisms. Model membranes represent attractive systems to study lipid nanodomains, which cannot be directly addressed in living cells with the currently available methods. This review summarizes the knowledge on lipid nanodomains in model membranes and exposes how their specific character contrasts with large-scale phase separation. The overview on lipid nanodomains in membranes composed of diverse lipids (e.g., zwitterionic and anionic glycerophospholipids, ceramides, glycosphingolipids) and cholesterol aims to evidence the impact of chemical, electrostatic, and geometric properties of lipids on nanodomain formation. Furthermore, the effects of curvature, asymmetry, and ions on membrane nanodomains are shown to be highly relevant aspects that may also modulate lipid nanodomains in cellular membranes. Potential mechanisms responsible for the formation and dynamics of nanodomains are discussed with support from available theories and computational studies. A brief description of current fluorescence techniques and analytical tools that enabled progress in lipid nanodomain studies is also included. Further directions are proposed to successfully extend this research to cells.
引用
收藏
页码:11259 / 11297
页数:39
相关论文
共 393 条
  • [1] Abbe E., 1873, ARCH MIKROSK ANAT, V9, P413, DOI [DOI 10.1007/BF02956173, 10.1007/BF02956173]
  • [2] Interactions of the EGFR juxtamembrane domain with PIP2-containing lipid bilayers: Insights from multiscale molecular dynamics simulations
    Abd Halim, Khairul Bariyyah
    Koldso, Heidi
    Sansom, Mark S. P.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2015, 1850 (05): : 1017 - 1025
  • [3] Central nervous system myelin: structure, synthesis and assembly
    Aggarwal, Shweta
    Yurlova, Larisa
    Simons, Mikael
    [J]. TRENDS IN CELL BIOLOGY, 2011, 21 (10) : 585 - 593
  • [4] Monte Carlo Simulation of Protein-Induced Lipid Demixing in a Membrane with Interactions Derived from Experiment
    Almeida, Paulo F.
    Best, Alexis
    Hinderliter, Anne
    [J]. BIOPHYSICAL JOURNAL, 2011, 101 (08) : 1930 - 1937
  • [5] GM1 Ganglioside Inhibits β-Amyloid Oligomerization Induced by Sphingomyelin
    Amaro, Mariana
    Sachl, Radek
    Aydogan, Gokcan
    Mikhalyov, Ilya I.
    Vacha, Robert
    Hof, Martin
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (32) : 9411 - 9415
  • [6] Lattice simulations of phase morphology on lipid bilayers: Renormalization, membrane shape, and electrostatic dipole interactions
    Amazon, Jonathan J.
    Feigenson, Gerald W.
    [J]. PHYSICAL REVIEW E, 2014, 89 (02):
  • [7] Cell biology - A role for lipid shells in targeting proteins to caveolae, rafts, and other lipid domains
    Anderson, RGW
    Jacobson, K
    [J]. SCIENCE, 2002, 296 (5574) : 1821 - 1825
  • [8] [Anonymous], 1999, Monte Carlo Methods in Statistical Physics
  • [9] Interaction between inclusions embedded in membranes
    ArandaEspinoza, H
    Berman, A
    Dan, N
    Pincus, P
    Safran, S
    [J]. BIOPHYSICAL JOURNAL, 1996, 71 (02) : 648 - 656
  • [10] Label-Free, All-Optical Detection, Imaging, and Tracking of a Single Protein
    Arroyo, J. Ortega
    Andrecka, J.
    Spillane, K. M.
    Billington, N.
    Takagi, Y.
    Sellers, J. R.
    Kukura, P.
    [J]. NANO LETTERS, 2014, 14 (04) : 2065 - 2070