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Specific removal of protein using protein imprinted polydopamine shells on modified amino-functionalized magnetic nanoparticles

机译:使用蛋白质印迹的聚多巴胺壳在修饰的氨基官能化磁性纳米粒子上特异性去除蛋白质

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摘要

Thin imprinted shells over functionalized magnetic nanoparticles is an effective solution to weaken mass transfer resistance, achieve high binding capacity, and attain rapid separation. In this work, a simple, green, and effective approach was developed to imprint bovine serum albumin (BSA) on the surface of amino-modified Fe3O4 nanoparticles (Fe3O4@NH2) using dopamine as monomer through a two-step immobilized template strategy. The results of X-ray diffraction and vibrating sample magnetometry indicated that the as-synthesized nanomaterials exhibited high crystallinity and satisfactory superparamagnetic properties. Transmission electron microscopy and Fourier transform infrared spectroscopy of the products showed that polydopamine shells successfully attached onto Fe3O4@NH2. The polydopamine shells with a thickness of about 10 nm enable the template recognition sites to be accessed easily, and exhibit fast kinetics and high adsorption capacity in aqueous solution. Meanwhile, an excellent selectivity towards BSA has been presented when bovine hemoglobin (BHb), transferrin, and immunoglobulin G (IgG) were employed as competitive proteins. Good recovery after a reasonably mild elution and successful capture of the target protein from a real sample of bovine blood suggests its potential value in practical applications. In addition, the resultant polymers were stable and had no obvious deterioration after six adsorption-regeneration cycles. The versatility of the proposed method has also been verified by choosing four other proteins with different isoelectric points as the templates.
机译:功能化磁性纳米颗粒上的薄压印外壳是降低传质阻力,实现高结合能力并实现快速分离的有效解决方案。在这项工作中,开发了一种简单,绿色且有效的方法,以多巴胺为单体,通过两步固定模板策略,将牛血清白蛋白(BSA)印在氨基修饰的Fe3O4纳米颗粒(Fe3O4 @ NH2)的表面上。 X射线衍射和振动样品磁测定的结果表明,所合成的纳米材料具有高结晶度和令人满意的超顺磁性能。产品的透射电子显微镜和傅里叶变换红外光谱表明,聚多巴胺壳成功地附着在Fe3O4 @ NH2上。厚度约为10 nm的聚多巴胺壳使模板识别位点易于进入,并在水溶液中具有快速的动力学和高吸附能力。同时,当牛血红蛋白(BHb),转铁蛋白和免疫球蛋白G(IgG)被用作竞争蛋白时,对BSA的选择性很好。经过适当温和的洗脱并从牛血的真实样品中成功捕获目标蛋白后,良好的回收率表明了其在实际应用中的潜在价值。另外,在六个吸附-再生循环之后,所得聚合物是稳定的并且没有明显的劣化。还通过选择其他四种具有不同等电点的蛋白质作为模板来验证了该方法的多功能性。

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