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Comparison of the Density of Proteins and Peptides Grafted on Silane Layers and Polyelectrolyte Multilayers

机译:硅烷层和聚电解质多层膜上嫁接的蛋白质和多肽的密度比较

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摘要

Immobilized proteins or peptides are of critical importance for applications such as biosensing or cell culture. We analyze the structure of layers of a large variety of proteins and peptides, grafted on silicon substrates by different routes differing in the nature of the intermediate layer linking the biomolecules to the substrate, either a silane monolayer, or a polyelectrolyte multilayer made from synthetic or natural polymers. The structural analysis is essentially performed by X-ray reflectometry, which proves to be an efficient methodology not requiring the use of tagged biomolecules, capable of evaluating consistently the amount of grafted biomolecules per surface area with estimated precisions ranging from 10 to 20%. The study provides a quantitative basis for selecting one among a series of well-proofed and sturdy grafting methodologies and underlines the potential of XRR for assessing the amount of grafted biomacromolecules without requiring the expensive tagging of molecules. Our results also show that, for the coupling route resting on synthetic polyelectrolytes, the grafting density is significantly lower than for direct coupling over a silane layer. In contrast, when performed over a cushion based on polysaccharides, the grafting density is well above the values found for a dense layer grafted on a silane monolayer, indicating partial penetration and swelling of the polysaccharide cushion.
机译:固定化的蛋白质或多肽对于诸如生物传感或细胞培养等应用至关重要。我们分析了通过不同途径接枝到硅基质上的各种蛋白质和肽层的结构,这些途径的不同之处在于将生物分子连接到基质的中间层的性质,即硅烷单层或由合成或合成的聚电解质多层天然聚合物。结构分析基本上是通过X射线反射仪进行的,这被证明是一种不需要使用标记生物分子的有效方法,能够以估计的精度从10%到20%不间断地评估每个表面积的接枝生物分子的数量。该研究为在一系列可靠且坚固的移植方法中选择一种提供了定量依据,并强调了XRR在无需昂贵的分子标记的情况下评估移植的生物大分子数量的潜力。我们的结果还表明,对于基于合成聚电解质的偶联途径,接枝密度显着低于在硅烷层上的直接偶联。相反,当在基于多糖的垫子上进行时,接枝密度远高于在硅烷单层上接枝的致密层的值,表明多糖垫子的部分渗透和溶胀。

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