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Molecule-specific darkfield and multiphoton imaging using gold nanocages

机译:使用金纳米笼的分子特定暗场和多光子成像

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Due to their robust optical properties, biological inertness, and readily adjustable surface chemistry, gold nanostructures have been demonstrated as contrast agents in a variety of biomedical imaging applications. One application is dynamic imaging of live cells using bioconjugated gold nanoparticles to monitor molecule trafficking mechanisms within cells; for instance, the regulatory pathway of epidermal growth factor receptor (EGFR) undergoing endocytosis. In this paper, we have demonstrated a method to track endocytosis of EGFR in MDA-MB-468 breast adenocarcinoma cells using bioconjugated gold nanocages (AuNCs) and multiphoton microscopy. Dynamic imaging was performed using a time series capture of 4 images every minute for 1 hour. Specific binding and internalization of the bioconjugated AuNCs was observed while the two control groups showed non-specific binding at fewer surface sites, leading to fewer bound AuNCs and no internalization.
机译:由于其强大的光学性能,生物惰性和易于调节的表面化学性质,金纳米结构已在各种生物医学成像应用中被证明是造影剂。一种应用是使用生物共轭金纳米粒子对活细胞进行动态成像,以监测细胞内的分子运输机制。例如,表皮生长因子受体(EGFR)经历胞吞作用的调节途径。在本文中,我们已经证明了使用生物共轭金纳米笼(AuNCs)和多光子显微镜在MDA-MB-468乳腺腺癌细胞中追踪EGFR内吞的方法。使用每分钟4张图像的时间序列捕获进行1小时的动态成像。观察到生物结合的AuNCs的特异性结合和内在化,而两个对照组在更少的表面位点显示出非特异性结合,导致更少的结合的AuNCs并且没有内在化。

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