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Biodegradable Tethered Lipid Bilayer–Microsphere Systems with Membrane-Integrated α-Helical Peptide Anchors

机译:具有膜整合的α-螺旋肽锚的可生物降解的栓系的脂质双层-微球系统

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摘要

Supported lipid bilayers (SLBs) are ideally suited for the study of biomembrane–biomembrane interactions and for the biomimicry of cell-to-cell communication, allowing for surface ligand displays that contain laterally mobile elements. However, the SLB paradigm does not include three-dimensionality and bio-compatibility. As a way to bypass these limitations, we have developed a biodegradable form of microsphere SLBs, also known as proteolipobeads (PLBs), using PLGA microspheres. Microspheres were synthesized using solvent evaporation and size selected with fluorescence activated cell sorting (FACS). Biomembranes were covalently tethered upon fusion to microsphere supports via short-chain PEG spacers connecting membrane-integrated α-helical peptides and the microsphere surface, affecting membrane diffusivity and mobility as indicated by confocal FRAP analysis. Membrane heterogeneities, which are attributed to PLGA hydrophobicity and rough surface topography, are curtailed by the addition of PEG tethers. This method allows for the presentation of tethered, laterally mobile biomembranes in three dimensions with functionally embedded attachment peptides for mobile ligand displays.
机译:支持的脂质双层(SLB)非常适合研究生物膜与生物膜的相互作用以及细胞与细胞之间的通信仿生,从而允许表面配体展示包含横向可移动的元素。但是,SLB范例不包括三维和生物相容性。作为绕过这些限制的一种方法,我们使用PLGA微球开发了可生物降解形式的微球SLB,也称为蛋白脂珠(PLB)。使用溶剂蒸发合成微球,并通过荧光激活细胞分选(FACS)选择大小。生物膜通过连接膜整合的α-螺旋肽和微球表面的短链PEG间隔子与微球载体融合后共价束缚,如共聚焦FRAP分析所示,影响膜的扩散性和迁移率。膜异质性归因于PLGA疏水性和粗糙的表面形貌,可通过添加PEG系链来减少。该方法允许在三维上呈现具有功能嵌入的附着肽的可横向束缚的横向移动生物膜,用于移动配体展示。

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