Gordon L M, Looney F D, Curtain C C
J Membr Biol. 1985;84(1):81-95. doi: 10.1007/BF01871650.
A model has been developed for 5-nitroxide stearate, I(12,3), distribution in human erythrocyte ghosts which accurately predicts ESR spectral alterations observed with increased probe/total lipid (P/L) at 37 degrees C. This spin probe occupies a class of high-affinity, noninteracting sites at low loading. Saturation occurs with increasing probe concentration, and, at higher loading, the probe inserts itself at initially dilute sites to form membrane-bound clusters of variable size. No 'low' probe remains at high P/L where all I(12,3) clusters in a 'concentrated' phase. This model allows determination of the dilute/clustered probe ratio, and shows that I(12,3) segregates in erythrocytes at what might otherwise be considered low P/L (e.g., 1/359). These findings validate the earlier use of empirical parameters to estimate probe sequestration in biological membranes.
已开发出一种用于5-硬脂酰氧基氮氧化物I(12,3)在人红细胞膜空壳中分布的模型,该模型能准确预测在37℃下随着探针/总脂质(P/L)增加所观察到的电子自旋共振(ESR)光谱变化。在低负载时,这种自旋探针占据一类高亲和力、不相互作用的位点。随着探针浓度增加会出现饱和现象,并且在较高负载时,探针会插入最初稀释的位点以形成大小可变的膜结合簇。在高P/L时没有“低”探针残留,此时所有I(12,3)簇处于“浓缩”相。该模型允许确定稀释/聚集探针的比例,并表明I(12,3)在红细胞中以可能被认为是低P/L(例如,1/359)的比例分离。这些发现证实了早期使用经验参数来估计生物膜中探针隔离情况的做法。