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Proteomic Characterization of Human Plasma Protein Adsorption onto Biomimetic Glycocalyx Surfaces

机译:人血浆蛋白吸附在仿生颗粒表面上的蛋白质组学表征

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Protein adsorption is fundamental to understand thrombosis and to design biocompatible materials for medical implants, devices, biosensors and drug delivery. We report a proteomic approach to characterize multiple human plasma proteins adsorbed onto four different types of model surfaces (silicon oxide, dextranized silicon, polyester-based polyurethane, and dextranized polyurethane) using two-dimensional electrophoresis and mass spectroscopy. The surfaces of silicon wafers and polyurethane were chemically modified with covalent attachment of dextran to the substrate to mimic the endothelial cell glycocalyx surface of a blood vessel lumen. Surface properties such as topography and hydrophobicity/hydrophilicity were determined and analyzed using atomic force microscopy and contact angle measurement. We show that dextranization of both silicon and polyurethane surfaces inhibits protein adsorption. These results suggest that dextran coatings for blood-contacting biomedical applications provide a promising approach for reducing inflammatory and thrombotic responses.
机译:蛋白质吸附是了解血栓形成和设计用于医疗植入物,装置,生物传感器和药物递送的生物相容性材料的基础。我们报告一个蛋白质组学的方法来表征吸附到使用二维电泳和质谱分析四种不同类型的模型的表面(氧化硅,硅dextranized,基于聚酯的聚氨酯和聚氨酯dextranized)多种人血浆蛋白。将硅晶片和聚氨酯的表面与葡聚糖的共价连接到基材上的化学改性以模拟血管腔的内皮细胞糖钙表面。使用原子力显微镜和接触角测量确定和分析地形和疏水性/亲水性的表面性质。我们表明硅和聚氨酯表面的含红细胞抑制蛋白质吸附。这些结果表明,用于血液接触生物医学应用的葡聚糖涂层提供了减少炎症和血栓抑制的有希望的方法。

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