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Development of dual-color simultaneous single molecule imaging system for analyzing multiple intracellular trafficking activities

机译:双彩同时单分子成像系统的开发分析多种细胞内贩运活动

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Intracellular trafficking is a critical process for cell physiology. Previous extensive studies employing biochemical and molecular biological approaches have provided qualitative information about intracellular trafficking, but we have little quantitative information due to technical limitations of these assays. We therefore developed a novel method for quantifying intracellular trafficking based on single molecule imaging with Quantum dot (QD) fluorescent nanocrystals and quantitatively described the trafficking properties of some recycling proteins. We herein first describe how to label intracellular molecules with QD which has no cell permeability and how to quantify intracellular trafficking, and then we detail the development of a novel experimental system allowing multi-color simultaneous single molecule imaging for analyzing the relationships of intracellular trafficking activities among multiple molecules having distinct trafficking properties. Finally, we document how we confirmed the reliability of our system by simultaneously analyzing the intracellular movements of two recycling protein, GLUT4 glucose transporter and transferrin receptor. Since impairment of intracellular trafficking has critical etiological roles in various late-onset diseases such as type 2 diabetes, our novel imaging system may be a powerful tool for developing next-generation biomedical devices for diagnostics and medical treatment based on intracellular trafficking.
机译:细胞内贩运是细胞生理学的关键过程。以前采用生化和分子生物学方法的广泛研究提供了有关细胞内贩运的定性信息,但由于这些测定的技术限制,我们具有很小的定量信息。因此,我们制定了一种基于单分子成像的量子分子成像与量子点(QD)荧光纳米晶体进行量化的新方法,并定量描述了一些回收蛋白的运输性能。我们首先描述如何用QD标记细胞内分子,所述QD没有细胞渗透性和如何量化细胞内运输,然后详细介绍了一种新型实验系统,允许多色同时单分子成像分析细胞内贩运活动的关系。在具有不同贩运性质的多种分子中。最后,我们通过同时分析两种回收蛋白,无菌4葡萄糖转运蛋白受体的细胞内运动来记录我们如何确认我们系统的可靠性。由于细胞内贩运的损害在各种后期疾病(如2型糖尿病)中具有关键的病因作用,我们的新型成像系统可能是开发基于细胞内运输的诊断和医疗的下一代生物医学装置的强大工具。

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