Plásek J, Jarolím P
Department of Biophysics, Charles University, Prague, Czechoslovakia.
Gen Physiol Biophys. 1987 Oct;6(5):425-37.
The relationship between the conditions of membrane labelling by the fluorescent probe 1,6-diphenyl-1,3,5-hexatriene (DPH) and its fluorescence parameters was investigated. In the labelling solutions prepared by the usual method, the presence of DPH microcrystals was revealed which led to the lower resultant fluorescence anisotropy values. Lower labelling efficiency was observed with DPH solutions in tetrahydrofuran when compared with solutions in acetone. Modifications of the labelling procedure are proposed which give better reproducibility of the results. There modified method involves the preparation of a 2 X 10(-4) mol. 1(-1) DPH stock solution in acetone, a 100-fold dilution in an appropriate buffer, subsequent bubbling through with nitrogen for 30 min and mixing the resulting solution with cell/membrane suspension in a 1:1 (v/v) ratio. Changes in intensity, anisotropy and spectra of DPH fluorescence in the course of membrane labelling were studied. A two-stage model of the incorporation of DPH into membranes was proposed, according to which DPH molecules first quickly adhere to the membrane surface and then are slowly translocated to the apolar regions of the membrane.
研究了荧光探针1,6 - 二苯基 - 1,3,5 - 己三烯(DPH)对膜的标记条件与其荧光参数之间的关系。在用常规方法制备的标记溶液中,发现存在DPH微晶,这导致最终的荧光各向异性值较低。与丙酮溶液相比,在四氢呋喃中的DPH溶液观察到较低的标记效率。提出了标记程序的改进方法,可使结果具有更好的重现性。改进后的方法包括在丙酮中制备2×10⁻⁴mol·L⁻¹的DPH储备溶液,在适当的缓冲液中稀释100倍,随后用氮气鼓泡30分钟,并将所得溶液与细胞/膜悬浮液按1:1(v/v)比例混合。研究了膜标记过程中DPH荧光强度、各向异性和光谱的变化。提出了DPH掺入膜的两阶段模型,根据该模型,DPH分子首先快速附着于膜表面,然后缓慢转移至膜的非极性区域。