Fluorescent Probes for Lipid Rafts: From Model Membranes to Living Cells

被引:405
作者
Klymchenko, Andrey S. [1 ]
Kreder, Remy [1 ]
机构
[1] Univ Strasbourg, Fac Pharm, UMR CNRS 7213, Lab Biophoton & Pharmacol, F-67401 Illkirch Graffenstaden, France
来源
CHEMISTRY & BIOLOGY | 2014年 / 21卷 / 01期
关键词
ION MASS-SPECTROMETRY; DETERGENT-RESISTANT MEMBRANES; GIANT UNILAMELLAR VESICLES; SINGLE-MOLECULE MICROSCOPY; ATOMIC-FORCE MICROSCOPY; PLASMA-MEMBRANE; CORRELATION SPECTROSCOPY; PHASE-SEPARATION; CHOLERA-TOXIN; CONFOCAL FLUORESCENCE;
D O I
10.1016/j.chembiol.2013.11.009
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
Membrane microdomains (rafts) remain one of the controversial issues in biophysics. Fluorescent molecular probes, which make these lipid nanostructures visible through optical techniques, are one of the tools currently used to study lipid rafts. The most common are lipophilic fluorescent probes that partition specifically into liquid ordered or liquid disordered phase. Their partition depends on the lipid composition of a given phase, which complicates their use in cellular membranes. A second class of probes is based on environment-sensitive dyes, which partition into both phases, but stain them by different fluorescence color, intensity, or lifetime. These probes can directly address the properties of each separate phase, but their cellular applications are still limited. The present review focuses on summarizing the current state in the field of developing and applying fluorescent molecular probes to study lipid rafts. We highlight an urgent need to develop new probes, specifically adapted for cell plasma membranes and compatible with modern fluorescence microscopy techniques to push the understanding of membrane microdomains forward.
引用
收藏
页码:97 / 113
页数:17
相关论文
共 127 条
[1]   EXTENSION OF THE PARALLAX ANALYSIS OF MEMBRANE PENETRATION DEPTH TO THE POLAR-REGION OF MODEL MEMBRANES - USE OF FLUORESCENCE QUENCHING BY A SPIN-LABEL ATTACHED TO THE PHOSPHOLIPID POLAR HEADGROUP [J].
ABRAMS, FS ;
LONDON, E .
BIOCHEMISTRY, 1993, 32 (40) :10826-10831
[2]   Fluorescent protein FRET pairs for ratiometric imaging of dual biosensors [J].
Ai, Hui-wang ;
Hazelwood, Kristin L. ;
Davidson, Michael W. ;
Campbell, Robert E. .
NATURE METHODS, 2008, 5 (05) :401-403
[3]   LIPOSOME ELECTROFORMATION [J].
ANGELOVA, MI ;
DIMITROV, DS .
FARADAY DISCUSSIONS, 1986, 81 :303-+
[4]  
[Anonymous], 2011, HDB FLUORESCENCE SPE
[5]   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
[6]   To see or not to see: Lateral organization of biological membranes and fluorescence microscopy [J].
Bagatolli, Luis A. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (10) :1541-1556
[7]   Fluorescence lifetime imaging microscopy: spatial resolution of biochemical processes in the cell [J].
Bastiaens, PIH ;
Squire, A .
TRENDS IN CELL BIOLOGY, 1999, 9 (02) :48-52
[8]   Imaging coexisting fluid domains in biomembrane models coupling curvature and line tension [J].
Baumgart, T ;
Hess, ST ;
Webb, WW .
NATURE, 2003, 425 (6960) :821-824
[9]   Fluorescence probe partitioning between Lo/Ld phases in lipid membranes [J].
Baumgart, Tobias ;
Hunt, Geoff ;
Farkas, Elaine R. ;
Webb, Watt W. ;
Feigenson, Gerald W. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2007, 1768 (09) :2182-2194
[10]   Large-scale fluid/fluid phase separation of proteins and lipids in giant plasma membrane vesicles [J].
Baumgart, Tobias ;
Hammond, Adam T. ;
Sengupta, Prabuddha ;
Hess, Samuel T. ;
Holowka, David A. ;
Baird, Barbara A. ;
Webb, Watt W. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (09) :3165-3170