How to determine diffusion coefficients in planar phospholipid systems by confocal fluorescence correlation spectroscopy

被引:194
作者
Benda, A
Benes, M
Marecek, V
Lhotsky, A
Hermens, WT
Hof, M
机构
[1] Acad Sci Czech Republ, J Heyrovsky Inst Phys Chem, CR-18223 Prague, Czech Republic
[2] Maastricht Univ, Res Ctr Complex Mol Syst & Biomol, NL-6200 MD Maastricht, Netherlands
[3] Maastricht Univ, Cardiovasc Res Inst Maastricht, NL-6200 MD Maastricht, Netherlands
关键词
D O I
10.1021/la0270136
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Confocal fluorescence correlation spectroscopy (FCS) allows for the determination of lateral diffusion coefficients and surface densities in planar phospholipid systems. The determination of the vertical (z-) position of the laser focus relative to the phospholipid surface plane is of crucial importance for the accuracy of the confocal FCS experiment. In this work we determine for the first time this vertical (z-) position of the laser focus by a so-called "Z-scan", which is based on the determination of diffusion times and particle numbers in 0.2 mum steps along the vertical (z-) axis. Experiments on supported phospholipid bilayers composed of dioleoylphosphatidylcholine (DOPC) and small amounts of Rhodamine Red-X 1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine, triethylammonium salt (Rhodamine Red-X DHPE) adsorbed onto atomically flat mica and borosilicate glass demonstrate that results obtained by the Z-scan approach are significantly more precise than those results obtained when the fluorescence intensity maximum is used as an indicator in the determination of the vertical (z-) position of the sample. In addition to this basic contribution for the investigation of planar bilayer systems by confocal FCS, the lateral diffusion coefficients of Rhodamine Red-X DHPE in supported phospholipid bilayers composed of DOPC and cholesterol as well as in DOPC or dipalmitoylphosphatidylcholine (DPPC) monolayers adsorbed at a liquid-liquid interface were determined.
引用
收藏
页码:4120 / 4126
页数:7
相关论文
共 32 条
  • [21] Formation of supported phospholipid bilayers from unilamellar vesicles investigated by atomic force microscopy
    Reviakine, I
    Brisson, A
    [J]. LANGMUIR, 2000, 16 (04) : 1806 - 1815
  • [22] Supported membranes: Scientific and practical applications
    Sackmann, E
    [J]. SCIENCE, 1996, 271 (5245) : 43 - 48
  • [23] ASSEMBLY AND MOLECULAR-ORGANIZATION OF SELF-ASSEMBLED LIPID BILAYERS ON SOLID SUBSTRATES MONITORED BY SURFACE-PLASMON RESONANCE SPECTROSCOPY
    SALAMON, Z
    WANG, Y
    TOLLIN, G
    MACLEOD, HA
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1195 (02): : 267 - 275
  • [24] Quantitative hybridization kinetics of DNA probes to RNA in solution followed by diffusional fluorescence correlation analysis
    Schwille, P
    Oehlenschlager, F
    Walter, NG
    [J]. BIOCHEMISTRY, 1996, 35 (31) : 10182 - 10193
  • [25] Schwille P, 1999, CYTOMETRY, V36, P176, DOI 10.1002/(SICI)1097-0320(19990701)36:3<176::AID-CYTO5>3.0.CO
  • [26] 2-F
  • [27] Critical micelle concentrations and stirring are rate-limiting in the loss of lipid mass during membrane degradation by phospholipase A(2)
    Speijer, H
    Giesen, PLA
    Zwaal, RFA
    Hack, CE
    Hermens, WT
    [J]. BIOPHYSICAL JOURNAL, 1996, 70 (05) : 2239 - 2247
  • [28] STANLEY M, 1980, REV SCI INSTRUM, V51, P98
  • [29] Impedance analysis of supported lipid bilayer membranes: A scrutiny of different preparation techniques
    Steinem, C
    Janshoff, A
    Ulrich, WP
    Sieber, M
    Galla, HJ
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1996, 1279 (02): : 169 - 180
  • [30] Thompson N.L., 1991, TOPICS FLUORESCENCE, V1, P337