Hutterer R, Schneider F W, Sprinz H, Hof M
Institute for Physical Chemistry, University of Wuerzburg, Germany.
Biophys Chem. 1996 Oct 30;61(2-3):151-60. doi: 10.1016/s0301-4622(96)02185-0.
The relative location, binding behaviour and the solvent relaxation behaviour of the polarity sensitive membrane probes 6-propionyl-2-(dimethylamino)naphthalene and 6-palmitoyl-2-[[trimethylammoniumethyl]methylamino]naphthalene chloride in vesicles composed of 1,2-dimyristoyl-sn-glycero-3-phosphatidylcholine or egg yolk lecithin have been compared using steady-state and time-resolved fluorescence as well as high resolution NMR measurements. The reconstructed time-resolved emission spectra show unambiguously that the observed spectral shifts in vesicle systems have to be assigned to time-dependent solvent relaxation processes rather than to a probe relocation mechanism. All fluorescence as well as the NMR relaxation data suggest a deeper localization of Patman in the membrane, sensing a less polar and/or more restricted probe environment.
使用稳态和时间分辨荧光以及高分辨率核磁共振测量,比较了极性敏感膜探针6-丙酰基-2-(二甲基氨基)萘和6-棕榈酰基-2-[[三甲基铵乙基]甲基氨基]萘氯化物在由1,2-二肉豆蔻酰基-sn-甘油-3-磷脂酰胆碱或蛋黄卵磷脂组成的囊泡中的相对位置、结合行为和溶剂弛豫行为。重构的时间分辨发射光谱明确表明,在囊泡系统中观察到的光谱位移必须归因于时间依赖性溶剂弛豫过程,而不是探针重新定位机制。所有荧光以及核磁共振弛豫数据表明,帕坦曼在膜中的定位更深,感知到的探针环境极性更小和/或限制更大。