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

机译:开发用于同时分析多种细胞内运输活动的双色同步单分子成像系统

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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:细胞内运输是细胞生理学的关键过程。以前使用生化和分子生物学方法进行的广泛研究已经提供了有关细胞内运输的定性信息,但是由于这些测定的技术局限性,我们几乎没有定量信息。因此,我们开发了一种基于量子点(QD)荧光纳米晶体的单分子成像定量细胞内运输的新方法,并定量描述了一些回收蛋白的运输特性。我们在此首先描述如何用没有细胞通透性的QD标记细胞内分子,以及如何量化细胞内运输,然后我们详细介绍了一种新型实验系统的开发,该系统允许进行多色同时单分子成像以分析细胞内运输活动的关系。在具有不同运输特性的多个分子中。最后,我们记录了我们如何通过同时分析两种循环蛋白GLUT4葡萄糖转运蛋白和转铁蛋白受体的细胞内运动来确认系统的可靠性。由于细胞内运输的损害在诸如2型糖尿病等各种迟发性疾病中具有关键的病因作用,因此我们新颖的成像系统可能是开发下一代生物医学设备的强大工具,用于基于细胞内运输的诊断和医学治疗。

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