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Probing the ethanol-induced chain interdigitations in gel-state bilayers of mixed-chain phosphatidylcholines.

机译:在混合链磷脂酰胆碱的凝胶态双层中探测乙醇诱导的链交叉。

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摘要

Using high-resolution differential scanning calorimetry (DSC), we have studied the effects of ethanol concentrations, [EtOH], on the main phase transition temperatures (T[m]) of the following mixed-chain phosphatidylcholines (PCs): C(15):C(17)PC, C(17):C(15)PC, and C(12):C(20)PC. These lipids have a common molecular weight; however, their apparent acyl chain-length differences between the sn-1 and sn-2 acyl chains, delta C, are distinctively different. The delta C values for these three mixed-chain PCs are, respectively, 0.5, 3.5, and 6.5 C-C bond lengths. DSC results show that the T(m) profiles for C(15):C(17)PC and C(17):C(15)PC bilayers in the plot of T(m) versus [EtOH] are V-shaped biphasic curves, with the minimum T(m) occurring at 50 and 73 mg/ml of ethanol, respectively. In contrast, the C(12):C(20)PC bilayer exhibits a nearly linear decrease in T(m) with increasing [EtOH]. In addition, x-ray diffraction experiments were also performed to assess the structural changes of these three mixed-chain PCs in the gel-state bilayers, at 20 degrees C, in response to high concentrations of ethanol. X-ray diffraction data indicate that, in the absence of ethanol, these three lamellar lipids are all packed in the normal (L beta') gel phase in aqueous media. In the presence of 120 mg/ml of ethanol, however, the C(15):C(17)PC and C(17):C(15)PC lamellae are packed in the fully interdigitated (L beta[I]) gel phase. The V-shaped T(m) curves detected calorimetrically for these two lipids in response to [EtOH] can thus be explained by the ethanol-induced L beta' --> L beta[I] isothermal phase transition. Interestingly, the results of x-ray diffraction study reveal, for the first time, that an ethanol-induced L beta' --> L(MI) (mixed interdigitated phase) isothermal phase transition occurs in the gel-state bilayer of highly asymmetrical C(12):C(20)PC. Therefore, the chain asymmetry is recognized to play an important role in the ethanol-induced chain interdigitation at T < T(m).
机译:使用高分辨率差示扫描量热法(DSC),我们研究了乙醇浓度[EtOH]对以下混合链磷脂酰胆碱(PCs)主相转变温度(T [m])的影响:C(15 ):C(17)PC,C(17):C(15)PC和C(12):C(20)PC。这些脂质具有共同的分子量。但是,它们在sn-1和sn-2酰基链之间的表观酰基链长度差异δC明显不同。这三个混合链PC的delta C值分别为0.5、3.5和6.5 C-C键长。 DSC结果表明,在T(m)与[EtOH]的图中,C(15):C(17)PC和C(17):C(15)PC双层的T(m)轮廓呈V形双相曲线,最小T(m)分别出现在50和73 mg / ml乙醇中。相反,随着[EtOH]的增加,C(12):C(20)PC双层膜的T(m)呈线性下降。此外,还进行了X射线衍射实验,以评估在20摄氏度时,响应于高浓度乙醇,这三种混合链PC在凝胶态双层中的结构变化。 X射线衍射数据表明,在没有乙醇的情况下,这三种层状脂质都被包装在水性介质中的正常(Lβ')凝胶相中。但是,在存在120 mg / ml乙醇的情况下,C(15):C(17)PC和C(17):C(15)PC薄片被填充在完全相互交叉的(L beta [I])凝胶中相。因此可以通过乙醇诱导的L beta'-> L beta [I]等温相变来解释对这两种脂质响应[EtOH]量热而测得的V形T(m)曲线。有趣的是,X射线衍射研究的结果首次揭示了乙醇诱导的Lβ'-> L(MI)(混合叉指相)等温相变发生在高度不对称的凝胶态双层中C(12):C(20)PC。因此,在T

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