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活细胞中不闪烁“巨型”量子点的三维追踪

3-Dimensional Tracking of Non-blinking 'Giant' Quantum Dots in Live Cells.

作者信息

Keller Aaron M, Ghosh Yagnaseni, DeVore Matthew S, Phipps Mary E, Stewart Michael H, Wilson Bridget S, Lidke Diane S, Hollingsworth Jennifer A, Werner James H

机构信息

Center for Integrated Nanotechnologies, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA.

Optical Sciences Division, Code 5600, US Naval Research Laboratory, Washington, D.C. 20375, USA.

出版信息

Adv Funct Mater. 2014 Aug 13;24(30):4796-4803. doi: 10.1002/adfm.201400349.

Abstract

While semiconductor quantum dots (QDs) have been used successfully in numerous single particle tracking (SPT) studies due to their high photoluminescence efficiency, photostability, and broad palette of emission colors, conventional QDs exhibit fluorescence intermittency or 'blinking,' which causes ambiguity in particle trajectory analysis and limits tracking duration. Here, non-blinking 'giant' quantum dots (gQDs) are exploited to study IgE-FcRI receptor dynamics in live cells using a confocal-based 3D SPT microscope. There is a 7-fold increase in the probability of observing IgE-FcRI for longer than 1 min using the gQDs compared to commercially available QDs. A time-gated photon-pair correlation analysis is implemented to verify that selected SPT trajectories are definitively from individual gQDs and not aggregates. The increase in tracking duration for the gQDs allows the observation of multiple changes in diffusion rates of individual IgE-FcRI receptors occurring on long (>1 min) time scales, which are quantified using a time-dependent diffusion coefficient and hidden Markov modeling. Non-blinking gQDs should become an important tool in future live cell 2D and 3D SPT studies, especially in cases where changes in cellular dynamics are occurring on the time scale of several minutes.

摘要

虽然半导体量子点(QDs)因其高光致发光效率、光稳定性和广泛的发射颜色调色板而成功应用于众多单粒子跟踪(SPT)研究中,但传统量子点表现出荧光间歇性或“闪烁”,这在粒子轨迹分析中会导致模糊性并限制跟踪持续时间。在此,利用不闪烁的“巨型”量子点(gQDs),使用基于共聚焦的3D SPT显微镜研究活细胞中的IgE-FcRI受体动力学。与市售量子点相比,使用gQDs观察IgE-FcRI超过1分钟的概率增加了7倍。实施时间门控光子对相关性分析以验证所选的SPT轨迹确实来自单个gQDs而非聚集体。gQDs跟踪持续时间的增加使得能够观察到单个IgE-FcRI受体在长(>1分钟)时间尺度上发生的扩散速率的多种变化,这些变化使用时间相关扩散系数和隐马尔可夫模型进行量化。不闪烁的gQDs应成为未来活细胞二维和三维SPT研究中的重要工具,特别是在细胞动力学变化发生在几分钟时间尺度的情况下。

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