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首页> 外文期刊>Acta biomaterialia >Protein interactions with layers of TiO2 nanotube and nanopore arrays: Morphology and surface charge influence
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Protein interactions with layers of TiO2 nanotube and nanopore arrays: Morphology and surface charge influence

机译:蛋白质与TiO2纳米管和纳米孔阵列的相互作用:形态和表面电荷的影响

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In the present work we investigate the key factors involved in the interaction of small-sized charged proteins with TiO2 nanostructures, i.e. albumin (negatively charged), histone (positively charged). We examine anodic nanotubes with specific morphology (simultaneous control over diameter and length, e.g. diameter 15, 50 or 100 nm, length 250 nm up to 10 mu m) and nanopores. The nanostructures surface area has a direct influence on the amount of bound protein, nonetheless the protein physical properties as electric charge and size (in relation to nanotopography and biomaterial's electric charge) are crucial too. The highest quantity of adsorbed protein is registered for histone, for 100 nm diameter nanotubes (10 mu m length) while higher values are registered for 15 nm diameter nanotubes when normalizing protein adsorption to nanostructures' surface unit area (evaluated from dye desorption measurements) consistent with theoretical considerations. The proteins presence on the nanostructures is evaluated by XPS and ToF-SIMS; additionally, we qualitatively assess their presence along the nanostructures length by ToF-S1MS depth profiles, with decreasing concentration towards the bottom.
机译:在当前的工作中,我们研究了与TiO2纳米结构(即白蛋白(带负电),组蛋白(带正电))相互作用的小电荷蛋白的关键因素。我们研究了具有特定形态的阳极纳米管(同时控制直径和长度,例如直径15、50或100 nm,长度250 nm至10μm)和纳米孔。纳米结构的表面积直接影响结合蛋白质的数量,但是蛋白质的物理性质也很重要,因为电荷和大小(与纳米形貌和生物材料的电荷有关)至关重要。对于组蛋白,直径为100 nm的纳米管(长度为10μm),组蛋白的吸附量最高;当对纳米结构的表面积单位面积进行归一化(根据染料解吸测量评估)时,对于直径为15 nm的纳米管,则具有更高的值。有理论上的考虑。通过XPS和ToF-SIMS评估纳米结构上蛋白质的存在;此外,我们通过ToF-S1MS深度剖面定性评估它们在纳米结构长度上的存在,并逐渐降低其浓度。

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