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Direct measurements of protein-stabilized gold nanoparticle interactions

机译:直接测量蛋白质稳定的金纳米粒子的相互作用

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We report integrated video and total internal reflection microscopy measurements of protein stabilized 110 nm Au nanoparticles confined in 280 nm gaps in physiological media. Measured potential energy profiles display quantitative agreement with Brownian dynamic simulations that include hydrodynamic interactions and camera exposure time and noise effects. Our results demonstrate agreement between measured nonspecific van der Waals and adsorbed protein interactions with theoretical potentials. Confined, lateral nanoparticle diffusivity measurements also display excellent agreement with predictions. These findings provide a basis to interrogate specific biomacromolecular interactions in similar experimental configurations and to design future improved measurement methods.
机译:我们报告集成的视频和全内反射显微镜测量的蛋白质稳定的110 nm Au纳米颗粒限制在生理介质中的280 nm的差距。测得的势能曲线与布朗动力学模拟显示出定量的一致性,其中包括流体动力学相互作用以及照相机暴露时间和噪声影响。我们的结果表明,测得的非特异性范德华力与吸附的蛋白相互作用具有理论潜力。受限的横向纳米颗粒扩散率测量也显示出与预测的极好的一致性。这些发现为在类似的实验配置中研究特定的生物大分子相互作用提供了基础,并为将来设计改进的测量方法提供了依据。

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