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Quantifying the cellular uptake of antibody-conjugated au nanocages by two-photon microscopy and inductively coupled plasma mass spectrometry

机译:通过双光子显微镜和电感耦合等离子体质谱法定量结合抗体的金纳米笼的细胞摄取

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Gold nanocages with localized surface plasmon resonance peaks in the near-infrared region exhibited a broad two-photon photoluminescence band extending from 450 to 650 nm when excited by a Ti: sapphire laser at 800 nm. The bright luminescence makes it possible to explore the use of Au nanocages as a new class of optical imaging agents for two-photon microscopy. In this work, we have demonstrated the use of twophoton microscopy as a convenient tool to directly examine the uptake of antibody-conjugated and PEGylated Au nanocages by U87MGwtEGFR cells. We have also correlated the results from two-photon microscopy with the data obtained by inductively coupled plasma mass spectrometry. Combined together, these results indicate that the antibody-conjugated Au nanocages were attached to the surface of the cells through antibody-antigen binding and then internalized into the cells via receptor-mediated endocytosis. The cellular uptake process was dependent on a number of parameters, including incubation time, incubation temperature, size of the Au nanocages, and the number of antibodies immobilized on each nanocage.
机译:在800 nm处的Ti:蓝宝石激光器激发时,在近红外区域具有局部表面等离振子共振峰的金纳米笼显示了从450到650 nm的宽双光子光致发光带。明亮的发光使得有可能探索使用Au纳米笼作为两类光子显微镜的新型光学成像剂。在这项工作中,我们已经证明了使用双光子显微镜作为一种便捷的工具,可以直接检查U87MGwtEGFR细胞对抗体偶联和PEG化Au纳米笼的摄取。我们还将两光子显微镜的结果与电感耦合等离子体质谱法获得的数据相关联。结合在一起,这些结果表明结合了抗体的金纳米笼通过抗体-抗原结合而附着于细胞表面,然后通过受体介导的内吞作用而被内化到细胞中。细胞摄取过程取决于许多参数,包括孵育时间,孵育温度,Au纳米笼的大小以及固定在每个纳米笼上的抗体数量。

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