Sassaroli M, Vauhkonen M, Perry D, Eisinger J
Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York 10029.
Biophys J. 1990 Feb;57(2):281-90. doi: 10.1016/S0006-3495(90)82530-3.
The lateral mobility of pyrenyl phospholipid probes in dimyristoylphosphatidylcholine (DMPC) vesicles was determined from the dependence of the pyrene monomeric and excimeric fluorescence yields on the molar probe ratio. The analysis of the experimental data makes use of the milling crowd model for two-dimensional diffusivity and the computer simulated random walks of probes in an array of lipids. The fluorescence yields for 1-palmitoyl-2-(1'-pyrenedecanoyl)phosphatidylcholine (py10PC) in DMPC bilayers are well fitted by the model both below and above the fluid-gel phase transition temperature (Tc) and permit the evaluation of the probe diffusion rate (f), which is the frequency with which probes take random steps of length L, the host membrane lipid-lipid spacing. The lateral diffusion coefficient is then obtained from the relationship D = fL2/4. In passing through the fluid-gel phase transition of DMPC (Tc = 24 degrees C), the lateral mobility of py10PC determined in this way decrease only moderately, while D measured by fluorescence photobleaching recovery (FPR) experiments is lowered by two or more orders of magnitude in gel phase. This difference in gel phase diffusivities is discussed and considered to be related either to (a) the diffusion length in FPR experiments being about a micrometer or over 100 times greater than that of excimeric probes (approximately 1 nm), or (b) to nonrandomicity in the distribution of the pyrenyl probes in gel phase DMPC. At 35 degrees C, in fluid DMPC vesicles, the diffusion rate is f = 1.8 x 10(8) s-1, corresponding to D = 29 microns2 s-1, which is about three times larger than the value obtained in FPR experiments. The activation energy for lateral diffusion in fluid DMPC was determined to be 8.0 kcal/mol.
通过芘单体和准分子荧光产率对摩尔探针比例的依赖性,测定了芘基磷脂探针在二肉豆蔻酰磷脂酰胆碱(DMPC)囊泡中的横向流动性。实验数据分析采用二维扩散的研磨群体模型以及脂质阵列中探针的计算机模拟随机游走。该模型对DMPC双层膜中1-棕榈酰-2-(1'-芘癸酰)磷脂酰胆碱(py10PC)在低于和高于流体-凝胶相转变温度(Tc)时的荧光产率均拟合良好,并允许评估探针扩散速率(f),即探针以主膜脂质-脂质间距L为步长进行随机步移的频率。然后根据关系式D = fL2/4获得横向扩散系数。在DMPC的流体-凝胶相转变(Tc = 24℃)过程中,通过这种方式测定的py10PC的横向流动性仅适度降低,而通过荧光漂白恢复(FPR)实验测得的D在凝胶相中降低了两个或更多数量级。讨论了凝胶相扩散率的这种差异,并认为其与以下因素有关:(a)FPR实验中的扩散长度约为1微米,比准分子探针的扩散长度(约1纳米)大100倍以上;或(b)芘基探针在凝胶相DMPC中的分布不具有随机性。在35℃时,在流体DMPC囊泡中,扩散速率为f = 1.8×10(8) s-1,对应D = 29微米2 s-1,约为FPR实验所得值的三倍。流体DMPC中横向扩散的活化能测定为8.0千卡/摩尔。