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脂筏相互作用的力。

Interaction Forces between Lipid Rafts.

机构信息

Department of Chemical Engineering, ‡Department of Chemistry, and §Department of Biomedical Engineering, University of California , Davis 95616, United States.

出版信息

Langmuir. 2017 Jan 10;33(1):382-387. doi: 10.1021/acs.langmuir.6b03717. Epub 2016 Dec 21.

Abstract

Cellular membranes containing sphingolipids and cholesterol have been shown to self-organize into lipid rafts-specialized domains that host integral membrane proteins and modulate the bioactivity of cells. In this work, force-distance profiles between raft membranes in the liquid-ordered phase consisting of singly unsaturated 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), a complex mixture of brain sphingomyelin (BSM), and cholesterol were measured using the surface force apparatus (SFA). Two distinct force profiles were detected corresponding to uniform raft membranes and raft membranes with a higher level of topological membrane defects (heterogeneous) as corroborated by atomic force microscopy (AFM) scans. In all cases a weak, long-range electrostatic repulsion was observed with some variation in the surface charge density. The variation in electrostatic repulsion was attributed to charged lipid species primarily from the constituent lipids in the BSM mixture. The adhesion between the uniform raft membranes was comparable to our previous work with pure component, liquid-ordered POPC-DPPC (1,2-dipalmitoyl-sn-glycero-3-phosphocholine)-cholesterol membranes. Raft membranes with more topological defects adhered more strongly owing to hydrophobic attraction between exposed acyl chains. Even though the rafts were in the liquid-ordered phase and membrane defects were present in the contact region, the raft membranes were stable, and no structural rearrangement was observed throughout the measurements. Our findings demonstrate that liquid-ordered membranes are stable to mechanical loading and not particularly sensitive to compositional variation.

摘要

含有神经鞘脂和胆固醇的细胞膜已被证明能够自组织成脂筏——一种特殊的域,其中包含整合膜蛋白并调节细胞的生物活性。在这项工作中,使用表面力仪(SFA)测量了由单一不饱和 1-棕榈酰基-2-油酰基-sn-甘油-3-磷酸胆碱(POPC)、脑鞘磷脂(BSM)的复杂混合物和胆固醇组成的有序相中的脂筏膜之间的力-距离曲线。检测到两种不同的力曲线,分别对应于均匀的脂筏膜和具有更高拓扑膜缺陷水平(异质)的脂筏膜,原子力显微镜(AFM)扫描结果对此进行了证实。在所有情况下,都观察到了微弱的长程静电排斥,表面电荷密度略有变化。静电排斥的变化归因于带电荷的脂质物种,主要来自 BSM 混合物中的组成脂质。均匀脂筏膜之间的粘附力与我们之前使用纯成分、有序相 POPC-DPPC(1,2-二棕榈酰基-sn-甘油-3-磷酸胆碱)-胆固醇膜的工作相当。由于暴露的酰基链之间的疏水吸引力,具有更多拓扑缺陷的脂筏膜粘附力更强。尽管脂筏处于有序相且在接触区域存在膜缺陷,但脂筏膜是稳定的,在整个测量过程中没有观察到结构重排。我们的研究结果表明,有序相膜能够承受机械加载,并且对组成变化不太敏感。

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