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流体磷脂酰胆碱/磷脂酰乙醇胺双层中超晶格排列的证据。

Evidence for superlattice arrangements in fluid phosphatidylcholine/phosphatidylethanolamine bilayers.

作者信息

Cheng K H, Ruonala M, Virtanen J, Somerharju P

机构信息

Department of Physics, Texas Tech University, Lubbock 79409, USA.

出版信息

Biophys J. 1997 Oct;73(4):1967-76. doi: 10.1016/S0006-3495(97)78227-4.

Abstract

Recently, evidence for cholesterol and phosphatidylcholine (PC) molecules to adapt superlattice arrangements in fluid lipid bilayers has been presented. Whether superlattice arrangements exist in other biologically relevant lipid membranes, such as phosphatidylethanolamine (PE)/PC, is still speculative. In this study, we have examined the physical properties of fluid 1-palmitoyl-2-oleoyl-PC (POPC) and 1-palmitoyl-2-oleoyl-PE (POPE) binary mixtures as a function of the POPE mole fraction (X(PE)) using fluorescence and Fourier transform infrared spectroscopy. At 30 degrees C, i.e., above the Tm of POPE and POPC, deviations, or dips, as well as local data scattering in the excimer-to-monomer fluorescence intensity ratio of intramolecular excimer forming dipyrenylphosphatidylcholine probe in POPE/POPC mixtures were detected at X(PE) approximately 0.04, 0.11, 0.16, 0.26, 0.33, 0.51, 0.66, 0.75, 0.82, 0.91, and 0.94. The above critical values of X(PE) coincide (within +/-0.03) with the critical mole fractions X(HX,PE) or X(R,PE) predicted by a headgroup superlattice model, which assumes that the lipid headgroups form hexagonal or rectangular superlattice, respectively, in the bilayer. Other spectroscopic data, generalized polarization of Laurdan and infrared carbonyl and phosphate stretching frequency, were also collected. Similar agreements between some of the observed critical values of X(PE) from these data and the X(HX,PE) or X(R,PE) values were also found. However, all techniques yielded critical values of X(PE) (e.g., 0.42 and 0.58) that cannot be explained by the present headgroup superlattice model. The effective cross-sectional area of the PE headgroup is smaller than that of the acyl chains. Hence, the relief of "packing frustration" of PE in the presence of PC (larger headgroup than PE) may be one of the major mechanisms in driving the PE and PC components to superlattice-like lateral distributions in the bilayer. We propose that headgroup superlattices may play a significant role in the regulation of membrane lipid compositions in cells.

摘要

最近,有证据表明胆固醇和磷脂酰胆碱(PC)分子可在流体脂质双层中形成超晶格排列。超晶格排列是否存在于其他生物学相关的脂质膜中,如磷脂酰乙醇胺(PE)/PC膜,仍有待推测。在本研究中,我们使用荧光和傅里叶变换红外光谱,研究了流体1-棕榈酰-2-油酰基-PC(POPC)和1-棕榈酰-2-油酰基-PE(POPE)二元混合物的物理性质随POPE摩尔分数(X(PE))的变化。在30摄氏度时,即高于POPE和POPC的熔点,在POPE/POPC混合物中,当X(PE)约为0.04、0.11、0.16、0.26、0.33、0.51、0.66、0.75、0.82、0.91和0.94时,检测到分子内准分子形成二芘磷脂酰胆碱探针的准分子与单体荧光强度比出现偏差或下降,以及局部数据散射。上述X(PE)的临界值与头基超晶格模型预测的临界摩尔分数X(HX,PE)或X(R,PE)相符(误差在±0.03以内),该模型假设脂质头基在双层中分别形成六边形或矩形超晶格。还收集了其他光谱数据,如劳丹的广义极化以及红外羰基和磷酸盐伸缩频率。从这些数据中观察到的一些X(PE)临界值与X(HX,PE)或X(R,PE)值之间也发现了类似的一致性。然而,所有技术都得出了目前头基超晶格模型无法解释的X(PE)临界值(例如0.42和0.58)。PE头基的有效横截面积小于酰基链的横截面积。因此,在PC(头基比PE大)存在的情况下,缓解PE的“堆积受挫”可能是驱动PE和PC组分在双层中形成类似超晶格横向分布的主要机制之一。我们提出,头基超晶格可能在细胞内膜脂质组成的调节中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a1a/1181097/3761dc56561e/biophysj00031-0277-a.jpg

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