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二油酰磷脂酰胆碱双层膜的结构、弯曲刚度和双层相互作用的温度依赖性。

Temperature dependence of structure, bending rigidity, and bilayer interactions of dioleoylphosphatidylcholine bilayers.

作者信息

Pan Jianjun, Tristram-Nagle Stephanie, Kucerka Norbert, Nagle John F

机构信息

Department of Physics, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, USA.

出版信息

Biophys J. 2008 Jan 1;94(1):117-24. doi: 10.1529/biophysj.107.115691. Epub 2007 Sep 7.

Abstract

X-ray diffuse scattering was measured from oriented stacks and unilamellar vesicles of dioleoylphosphatidylcholine lipid bilayers to obtain the temperature dependence of the structure and of the material properties. The area/molecule, A, was 75.5 A(2) at 45 degrees C, 72.4 A(2) at 30 degrees C, and 69.1 A(2) at 15 degrees C, which gives the area expansivity alpha(A) = 0.0029/deg at 30 degrees C, and we show that this value is in excellent agreement with the polymer brush theory. The bilayer becomes thinner with increasing temperature; the contractivity of the hydrocarbon portion was alpha(Dc) = 0.0019/deg; the difference between alpha(A) and alpha(Dc) is consistent with the previously measured volume expansivity alpha(Vc) = 0.0010/deg. The bending modulus K(C) decreased as exp(455/T) with increasing T (K). Our area compressibility modulus K(A) decreased with increasing temperature by 5%, the same as the surface tension of dodecane/water, in agreement again with the polymer brush theory. Regarding interactions between bilayers, the compression modulus B as a function of interbilayer water spacing D'(W) was found to be nearly independent of temperature. The repulsive fluctuation pressure calculated from B and K(C) increased with temperature, and the Hamaker parameter for the van der Waals interaction was nearly independent of temperature; this explains why the fully hydrated water spacing, D'(W), that we obtain from our structural results increases with temperature.

摘要

对二油酰磷脂酰胆碱脂质双层的定向堆叠和单层囊泡进行了X射线漫散射测量,以获得结构和材料特性的温度依赖性。在45℃时,每个分子的面积A为75.5 Ų,在30℃时为72.4 Ų,在15℃时为69.1 Ų,由此得出在30℃时面积膨胀系数α(A)=0.0029/℃,并且我们表明该值与聚合物刷理论非常吻合。随着温度升高,双层变薄;烃部分的收缩率为α(Dc)=0.0019/℃;α(A)和α(Dc)之间的差异与先前测量的体积膨胀系数α(Vc)=0.0010/℃一致。弯曲模量K(C)随着温度T(开尔文)升高按exp(455/T)下降。我们的面积压缩模量K(A)随着温度升高下降了5%,与十二烷/水的表面张力相同,这再次与聚合物刷理论一致。关于双层之间的相互作用,发现压缩模量B作为双层间水间距D'(W)的函数几乎与温度无关。由B和K(C)计算出的排斥波动压力随温度升高而增加,范德华相互作用的哈梅克参数几乎与温度无关;这解释了我们从结构结果中得到的完全水合水间距D'(W)为何随温度升高。

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