Mekler V M, Kotel'nikov A I, Likhtenshteĭn G I, Berkovich M A
Biofizika. 1982 Jul-Aug;27(4):641-5.
Possibility of using phosphorescent probes for membrane investigations was analysed on lecithin liposomes and rat liver microsomes taken as an example. It was shown that one quencher molecule on 10(4) lecithin molecules is sufficient for experimental registration of diffusion-controlled quenching of erythrosine phosphorescence by stable nitroxide radicals. It is possible to study the diffusion processes with D = 10(-5) divided by 10(-9) cm2s-1. Application of quenchers of different polarity allows to make a conclusion that the phosphorescent probe erythrosine is localized in liposomes in the region of polar heads of phosphatidyl choline. It was determined from the rate of phosphorescence quenching by radicals that the membrane microviscosity in this region at 20 degrees C equals approximately 1 puas. The coefficient of erythrosine lateral diffusion in liposomes estimated from their self-quenching equals 1,1 x 10(-8) cm2s-1. In the microsome erythrosine is localized in hydrophobic parts of proteins and is not accessible for the quencher molecules.
以卵磷脂脂质体和大鼠肝脏微粒体为例,分析了使用磷光探针进行膜研究的可能性。结果表明,每10⁴个卵磷脂分子中有一个猝灭剂分子就足以通过稳定的氮氧化物自由基对赤藓红磷光进行扩散控制猝灭的实验记录。可以研究扩散系数D = 10⁻⁵至10⁻⁹ cm²/s的扩散过程。应用不同极性的猝灭剂可以得出结论,磷光探针赤藓红位于脂质体中磷脂酰胆碱极性头部区域。根据自由基猝灭磷光的速率确定,该区域在20℃时的膜微粘度约为1泊。根据脂质体的自猝灭估算,赤藓红在脂质体中的横向扩散系数为1.1×10⁻⁸ cm²/s。在微粒体中,赤藓红位于蛋白质的疏水部分,猝灭剂分子无法接近。