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二棕榈酰磷脂酰胆碱双层膜的界面区域受到促融性两亲分子的干扰。

The interfacial region of dipalmitoylphosphatidylcholine bilayers is perturbed by fusogenic amphipaths.

作者信息

Lentz B R, Wu J R, Zheng L, Prevrátil J

机构信息

Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill 27599-7260, USA.

出版信息

Biophys J. 1996 Dec;71(6):3302-10. doi: 10.1016/S0006-3495(96)79522-X.

Abstract

Several structural methods were used to probe the influence of three fusogenic and four nonfusogenic amphipaths on large, unilamellar dipalmitoylphosphatidylcholine (DPPC) vesicles. For four of these structural measurements there was a correlation observed between the ability of an amphipath to favor poly(ethylene glycol) (PEG)-induced fusion and the structural perturbation reported by each method. First, the fluorescence anisotropy of 1-[4-(trimethylamino)phenyl]-6-phenyhexa-1,3,5-triene (TMA-DPH), which probes the upper region of the bilayer, decreased in the range of PEG concentrations previously found to cause fusion of membranes containing fusogenic amphipaths. For nonfusogenic amphipaths, the anisotropy increased monotonically with PEG concentration. The properties of similar probes that locate in the hydrophobic core of the bilayer showed no correlation with fusogenicity, nor did the properties of probes purported to sense the aqueous surface of the membrane. Second, the frequency of the C=O stretch increased and then decreased dramatically as fusogenic but not nonfusogenic membranes were heated through their phase transition. Third, there was a dramatic increase in the frequency of the C-O-C ester stretch at the membrane order/disorder phase transition for membranes containing fusogenic amphipaths, twice the increase observed for nonfusogenic amphipaths. The spectral characteristics of phosphate, choline, and acyl chain motions showed no such correlation with fusogenicity. Finally, calorimetric measurements showed that low levels of fusogenic amphipaths eliminated the "pretransition" (L beta-->P beta) in DPPC membranes, whereas other amphipaths shifted but did not eliminate this transition. Taken together, these results indicate that fusogenic amphipaths perturb the interface or "backbone" region of the bilayer rather than the hydrophobic core, the headgroup, or the water interface regions of DPPC bilayers.

摘要

采用了几种结构方法来探究三种促融合性两亲分子和四种非促融合性两亲分子对大单层二棕榈酰磷脂酰胆碱(DPPC)囊泡的影响。在这些结构测量中的四项中,观察到两亲分子促进聚乙二醇(PEG)诱导融合的能力与每种方法所报告的结构扰动之间存在相关性。首先,1-[4-(三甲基氨基)苯基]-6-苯基己-1,3,5-三烯(TMA-DPH)的荧光各向异性用于探测双层膜的上层区域,在先前发现会导致含有促融合性两亲分子的膜发生融合的PEG浓度范围内降低。对于非促融合性两亲分子,各向异性随PEG浓度单调增加。位于双层膜疏水核心中的类似探针的性质与促融合性无关,据称能感知膜水表面的探针性质也无关。其次,当促融合性而非非促融合性膜通过其相变加热时,C=O伸缩振动的频率先增加然后急剧下降。第三,对于含有促融合性两亲分子的膜,在膜的有序/无序相变处C-O-C酯伸缩振动的频率急剧增加,是非促融合性两亲分子观察到的增加量的两倍。磷酸盐、胆碱和酰基链运动的光谱特征与促融合性没有这种相关性。最后,量热测量表明,低水平的促融合性两亲分子消除了DPPC膜中的“预转变”(Lβ→Pβ),而其他两亲分子使这种转变发生了移动但并未消除。综上所述,这些结果表明,促融合性两亲分子扰乱了双层膜的界面或“主链”区域,而不是DPPC双层膜的疏水核心、头部基团或水界面区域。

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