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Influence of the Preparation Route on the Supramolecular Organization of Lipids in a Vesicular System

机译:制备途径对囊泡系统脂质超分子组织的影响

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摘要

A confocal fluorescence microscopy-based assay was used for studying the influence of the preparation route on the supramolecular organization of lipids in a vesicular system. In this work, vesicles composed of cholesterol and CTAB (l/l mol %) or cholesterol and DOPC (2/8 mol %) and incorporating two membrane dyes were prepared by either a compressed fluid (CF)-based method (DELOS-susp) or a conventional film hydration procedure. They were subsequently immobilized and imaged individually using a confocal fluorescence microscope. Two integrated fluorescence intensities, I_(dye1) and I_(dye2), were assigned to each tracked vesicle, and their ratio, I_(dye1)/I_(dye2)was used for quantifying the degree of membrane inhomogeneity between individual vesicles within each sample. A distribution of I_(dye1)/I_(dye2) values was obtained for all the studied vesicular systems, indicating intrasample heterogeneity. The degree of inhomogeneity (DI) was similar for Chol/DOPC vesicles prepared by both procedures. In contrast, DI was more than double for the hydration method compared to the CF-based method in the case of Chol/CTAB vesicles, which can suffer from lipid demixing during film formation. These findings reveal a more homogeneous vesicle formation path by CFs, which warranted good homogeneity of the vesicular system, independently of the lipid mixture used.
机译:基于共聚焦荧光显微镜的测定法用于研究制备途径对囊泡系统中脂质的超分子组织的影响。在这项工作中,通过基于压缩流体(CF)的方法(DELOS-susp)制备了由胆固醇和CTAB(1 / l mol%)或胆固醇和DOPC(2/8 mol%)组成并掺入两种膜染料的囊泡。 )或传统的薄膜水化程序。随后将它们固定并使用共聚焦荧光显微镜分别成像。将两个积分荧光强度I_(dye1)和I_(dye2)分配给每个跟踪的囊泡,并将它们的比率I_(dye1)/ I_(dye2)用于量化每个样品中各个囊泡之间的膜不均匀程度。 。对于所有研究的囊泡系统,均获得了I_(dye1)/ I_(dye2)值的分布,表明样品内存在异质性。通过两种方法制备的Chol / DOPC囊泡的不均匀度(DI)相似。相比之下,在Chol / CTAB囊泡的情况下,与基于CF的方法相比,水合方法的DI超过两倍,后者在成膜过程中可能会发生脂质分解。这些发现揭示了CFs更均匀的囊泡形成途径,其保证了囊泡系统的良好均质性,而与所使用的脂质混合物无关。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第4期|p.1918-1921|共4页
  • 作者单位

    Department of Molecular Nanoscience and Organic Materials (ICMAB-CSIC), Bellaterra, 08193, Spain,CIBER de Bioingenieria, Biomateriales y Nanomedicina (CIBER-BBN), Bellaterra, 08193, Spain;

    Bio-Nanotechnology Laboratory, Department of Neuroscience and Pharmacology, University of Copenhagen, 2100 Copenhagen, Denmark,Nano-Science Center, University of Copenhagen, 2100 Copenhagen, Denmark,Lundbeck Foundation Center Biomembranes in Nanomedicine, University of Copenhagen, 2100 Copenhagen, Denmark;

    Bio-Nanotechnology Laboratory, Department of Neuroscience and Pharmacology, University of Copenhagen, 2100 Copenhagen, Denmark,Nano-Science Center, University of Copenhagen, 2100 Copenhagen, Denmark,Lundbeck Foundation Center Biomembranes in Nanomedicine, University of Copenhagen, 2100 Copenhagen, Denmark;

    Department of Molecular Nanoscience and Organic Materials (ICMAB-CSIC), Bellaterra, 08193, Spain,CIBER de Bioingenieria, Biomateriales y Nanomedicina (CIBER-BBN), Bellaterra, 08193, Spain;

    Nano-Science Center, University of Copenhagen, 2100 Copenhagen, Denmark,Department of Chemistry, University of Copenhagen, 2100 Copenhagen, Denmark;

    Department of Molecular Nanoscience and Organic Materials (ICMAB-CSIC), Bellaterra, 08193, Spain,CIBER de Bioingenieria, Biomateriales y Nanomedicina (CIBER-BBN), Bellaterra, 08193, Spain;

    Bio-Nanotechnology Laboratory, Department of Neuroscience and Pharmacology, University of Copenhagen, 2100 Copenhagen, Denmark,Nano-Science Center, University of Copenhagen, 2100 Copenhagen, Denmark,Lundbeck Foundation Center Biomembranes in Nanomedicine, University of Copenhagen, 2100 Copenhagen, Denmark;

    Department of Molecular Nanoscience and Organic Materials (ICMAB-CSIC), Bellaterra, 08193, Spain,CIBER de Bioingenieria, Biomateriales y Nanomedicina (CIBER-BBN), Bellaterra, 08193, Spain;

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