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A quantitative analysis of the intracellular transport of quantum dot-peptide in live cells using total internal reflection and confocal microscopy

机译:使用全内反射和共聚焦显微镜对活细胞中量子点肽细胞内传输的定量分析

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For investigatoin of intracellular protein interactions, quantum dots are widely used for fluorescent live cell imaging such as total internal reflection fluorescence (TIRF) microscopy and confocal microscopy. In this paper, we performed a quantitative analysis based on fluorescent intensity. For the measurement, A431 cell lines are imaged live with quantum dots using TIRF microscopy. The distribution of quantum dots is affected by a TATHA2 peptide sequence in live cells. This paper also presents the location change of quantum dots due to a nuclear localization signal in A431 cell lines. Confocal microscopy was used to confirm the relation with fluorescent intensity and quantum dot concentration in live cells.
机译:对于细胞内蛋白质相互作用的研究,量子点广泛用于荧光活细胞成像,例如全内反射荧光(TIRF)显微镜和共聚焦显微镜。 在本文中,我们基于荧光强度进行了定量分析。 对于测量,使用Tirf显微镜,A431细胞系成像与量子点一起生活。 量子点的分布受到活细胞中的酪蛋白肽序列的影响。 本文还提出了由于A431细胞系中的核定位信号引起的量子点的位置变化。 共聚焦显微镜用于确认活细胞中荧光强度和量子点浓度的关系。

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