Stubbs G W, Litman B J
Biochemistry. 1976 Jun 29;15(13):2766-72. doi: 10.1021/bi00658a009.
The microviscosity of the hydrocarbon region of the bovine retinal rod outer segment disk membrane was determined by measuring the anisotropy of fluorescence from the probe 1,6-diphenyl-1,3,5-hexatriene. The microviscosity ranged from 1.4 P at 40 degreeC to 15 P at O degree C, and no phase transition was observed in this temperature range. Bleaching of rhodopsin in the disk membrane produced no change in the microviscosity within the limits of error of our measurement (not equal to 5%). The presence of retinal in the disk membrane caused string quenching of the probe fluorescence. Removal of retinal from bleached disks produced a threefold increase in total fluorescence intensity and only a 10% drop in fluorescnece anisotropy, suggesting that large lateral gradients in microviscosity do not exist in the disk membrane. Bilayers prepared from extracted disk lipids had a microviscosity which was about one-fourth that of the intact disk membrane, demonstrating that rhodopsin hinders the mobility of the hydrocarbon chains of the disk phospholipids or egg phosphatidylcholine had identical microviscosities despite the much higher degree of unsaturation of the disk phospholipids.
通过测量探针1,6 - 二苯基 - 1,3,5 - 己三烯荧光的各向异性,测定了牛视网膜视杆细胞外段盘膜碳氢化合物区域的微粘度。微粘度范围从40℃时的1.4泊到0℃时的15泊,在此温度范围内未观察到相变。在我们测量误差范围内(±5%),盘膜中视紫红质的漂白未引起微粘度的变化。盘膜中视黄醛的存在导致探针荧光的串淬灭。从漂白的盘膜中去除视黄醛使总荧光强度增加了三倍,而荧光各向异性仅下降了10%,这表明盘膜中不存在大的微粘度横向梯度。由提取的盘膜脂质制备的双层膜的微粘度约为完整盘膜微粘度的四分之一,这表明视紫红质阻碍了盘膜磷脂烃链的流动性,或者尽管盘膜磷脂的不饱和程度高得多,但与卵磷脂具有相同的微粘度。