Fraser D M, Louro S R, Horváath L I, Miller K W, Watts A
Department of Biochemistry, University of Oxford, U.K.
Biochemistry. 1990 Mar 20;29(11):2664-9. doi: 10.1021/bi00463a007.
Stearic acid, phosphatidylcholine, and phosphatidylglycerol nitroxide spin-labels were used to probe the effect of 1-hexanol, urethane, diethyl ether, and ethanol on lipid-protein interactions in nicotinic acetylcholine receptor (nAcChoR) rich membranes from Torpedo nobiliana. For stearic acid spin-labeled at the C-14 position of the sn-1 acyl chain, 1-hexanol induced little change (over a wide concentration range, 0-16.7 mM) in either the ESR line shape or the proportion of motionally restricted spectral component from labels probing the protein interface. The main effect of 1-hexanol was limited to an increase in the mobility of stearic acid spin-labels probing the non-protein-associated environment. In contrast, for C-14 phosphatidylcholine spin-label, 1-hexanol decreased the fraction of spin-labels motionally restricted at the protein interface from 0.33 without 1-hexanol to 0.20 with 16.7 mM 1-hexanol, with no change in the line shape of the spectral component of these labels. The ESR spectral line shape of the fluid component due to phosphatidylcholine labels in sites away from the protein interface displayed a gradual decrease in spectral anisotropy on addition of increasing amounts of 1-hexanol. At a concentration of 1-hexanol that desensitizes half the receptors, the fraction of motionally restricted phosphatidylcholine spin-label is reduced by approximately 15%. The effect of 1-hexanol on phosphatidylglycerol spin-labels was intermediate between these two cases. Similar effects were measured with other general anesthetics, including urethane, diethyl ether, and ethanol.(ABSTRACT TRUNCATED AT 250 WORDS)
硬脂酸、磷脂酰胆碱和磷脂酰甘油氮氧自由基自旋标记物被用于探究1-己醇、氨基甲酸乙酯、乙醚和乙醇对来自电鳐富含烟碱型乙酰胆碱受体(nAcChoR)的膜中脂质-蛋白质相互作用的影响。对于在sn-1酰基链的C-14位置自旋标记的硬脂酸,在较宽浓度范围(0-16.7 mM)内,1-己醇对ESR谱线形状或探测蛋白质界面的标记物的运动受限光谱成分比例几乎没有影响。1-己醇的主要作用仅限于增加探测非蛋白质相关环境的硬脂酸自旋标记物的流动性。相比之下,对于C-14磷脂酰胆碱自旋标记物,1-己醇使在蛋白质界面运动受限的自旋标记物比例从无1-己醇时的0.33降至含16.7 mM 1-己醇时的0.20,而这些标记物光谱成分的谱线形状没有变化。远离蛋白质界面位点的磷脂酰胆碱标记物产生的流体成分的ESR光谱谱线形状在加入越来越多的1-己醇后显示出光谱各向异性逐渐降低。在使一半受体脱敏的1-己醇浓度下,运动受限的磷脂酰胆碱自旋标记物比例降低约15%。1-己醇对磷脂酰甘油自旋标记物的影响介于这两种情况之间。用其他全身麻醉剂(包括氨基甲酸乙酯、乙醚和乙醇)也测得类似效果。(摘要截短于250词)