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苯甲醇诱导脂质交错相潜在因素的热力学和荧光研究

Thermodynamic and fluorescence studies of the underlying factors in benzyl alcohol-induced lipid interdigitated phase.

作者信息

Chen C H, Hoye K, Roth L G

机构信息

Wadsworth Center, New York State Department of Health, Albany, USA.

出版信息

Arch Biochem Biophys. 1996 Sep 15;333(2):401-6. doi: 10.1006/abbi.1996.0407.

Abstract

To further investigate factors contributing to the action of alcohol in the solute-induced lipid interdigitation phase, thermodynamic and fluorescence polarization measurements were carried out to study the interaction of benzyl alcohol with dipalmitoyl phosphatidylcholine bilayer vesicles. The obtained results were compared with those previously reported for ethanol and cyclohexanol (L. G. Roth and C-H. Chen, Arch. Biochem. Biophys. 296, 207, 1992). Similar to ethanol, benzyl alcohol was found to exhibit a biphasic effect on the enthalpy (delta Hm) and the temperature (tm) of the lipid-phase transition and the steady-state fluorescence polarization (P) monitored by 1,6-diphenyl-1,3,5-hexatriene. At a total concentration of benzyl alcohol < 30 mg/ml (the alcohol concentration in lipid phase < 21 mg/ml), benzyl alcohol was found to exhibit large increases in delta Hm and P, which were correlated with the formation of a lipid interdigitated phase, as evidenced by reported X-ray diffraction data. Combining the results with benzyl alcohol and ethanol suggested that simultaneously large changes in delta Hm and P can be used as an indication of the occurrence of a solute-induced lipid interdigitated phase. The overall interacting force in the formation of this lipid phase, as derived from the interactions of the hydroxyl portion of an alcohol with the lipid phosphate head group and the hydrophobic portion of an alcohol with the lipid hydrocarbon chains, may or may not be dominated by hydrophobic interaction. Although lipid/water partition coefficients and the contribution of hydrophobic interaction to the overall interacting force were comparable between benzyl alcohol and cyclohexanol, benzyl alcohol induced lipid interdigitated phase, but not for cyclohexanol. This was due to the ability of benzyl alcohol to be more effective than cyclohexanol in simultaneously interacting with the phosphate head group and the hydrocarbon chains of lipid.

摘要

为了进一步研究导致酒精在溶质诱导的脂质交叉指状相起作用的因素,进行了热力学和荧光偏振测量,以研究苯甲醇与二棕榈酰磷脂酰胆碱双层囊泡的相互作用。将所得结果与先前报道的乙醇和环己醇的结果进行了比较(L.G.罗斯和陈C-H,《生物化学与生物物理学报》296, 207, 1992)。与乙醇相似,发现苯甲醇对脂质相变的焓(ΔHm)和温度(tm)以及由1,6-二苯基-1,3,5-己三烯监测的稳态荧光偏振(P)呈现双相效应。当苯甲醇的总浓度<30mg/ml(脂质相中的酒精浓度<21mg/ml)时,发现苯甲醇的ΔHm和P大幅增加,这与脂质交叉指状相的形成相关,如报道的X射线衍射数据所证明。将苯甲醇和乙醇的结果相结合表明,ΔHm和P同时发生的大幅变化可作为溶质诱导的脂质交叉指状相出现的指示。由醇的羟基部分与脂质磷酸头部基团的相互作用以及醇的疏水部分与脂质烃链的相互作用产生的形成该脂质相的整体相互作用力,可能由疏水相互作用主导,也可能不由其主导。尽管苯甲醇和环己醇之间的脂质/水分配系数以及疏水相互作用对整体相互作用力的贡献相当,但苯甲醇能诱导脂质交叉指状相,而环己醇则不能。这是因为苯甲醇比环己醇更能有效地同时与脂质的磷酸头部基团和烃链相互作用。

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