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Label-free in-flow detection of receptor recognition motifs on the biomolecular corona of nanoparticles

机译:Label-free子检测受体识别生物分子电晕的图案纳米粒子

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摘要

Nanomedicine, nanotargeting and nanotherapeutics have in the last few years faced several difficulties in translating the promising results obtained in vitro to an in vivo scenario. The origin of this discrepancy might be found in the lack of a detailed and realistic characterization of the biological surface of nanoparticles. Despite the capability to engineer nanomaterials with a great variety and a precise control of the surface functionalization, the targeting capability is lost when the nanoparticles are embedded in complex biological media, due to the formation of a biological layer (biomolecular corona). This biological layer represents the ultimate nanoparticle surface, likely to interact with the cell machinery. Therefore, in addition to traditional nanoparticle characterization techniques, a more insightful investigation of the biomolecular corona is needed, including the capability to assess the orientation and functionality of specific key molecular features. Here we present a method for the rapid screening of exposed protein recognition motifs on the surface of nanoparticles exploiting quartz crystal microbalance (QCM). We quantify accessible functional epitopes of transferrin-coated nanoparticles and correlate them to differences in nanoparticle size and functionalization. The target recognition occurs label free in flow, thereby pushing our investigation into a more in vivo-like scenario. Our method is applicable to a wide array of nanoparticles and therefore holds the potential to become an advanced technique for the classification of all kinds of nanobioconstructs based on their biological external functionality.
机译:纳米医学,nanotargeting和纳米疗法在过去的几年里面临几个吗翻译的困难有前途的结果获得体外到体内的场景。这种差异的起源可能会发现的缺乏详细的和现实的特征的生物纳米粒子表面。尽管纳米材料工程师的能力各种和精确的控制表面功能化,瞄准功能是当纳米粒子嵌入在复杂生物媒体,由于一个生物层(生物分子的形成电晕)。最终的纳米颗粒表面,可能会相互作用与细胞机械。传统的纳米表征技术,更为深刻的调查生物分子电晕是必要的,包括评估取向和能力特定的关键分子的功能特性。在这里,我们提出一个快速筛选方法暴露出蛋白质的识别上的图案纳米粒子表面利用石英水晶微量天平(药物)。访问功能抗原表位transferrin-coated纳米颗粒和关联纳米颗粒大小和差异功能化。标签中自由流动,从而推动我们调查在vivo-like场景中。我们的方法适用于广泛的纳米粒子,因此有潜力成为一个先进的技术分类各种nanobioconstructs基于生物外部功能。

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