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Quantum dot labeling based on near-field optical imaging of CD44 molecules

机译:基于CD44分子近场光学成像的量子点标记

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摘要

The lateral organization of membrane proteins and lipids domains has a direct impact on many cellular processes, but generally these domains are too small to be resolved by diffraction-limited resolution of fluorescence microscopy. Here, we use quantum dot (QD) labeling based on near-field optical imaging, to study the nanoscale organization of hyaluronan receptor CD44 molecules of fixed mesenchymal stem cells (MSCs) in air, with a optical resolution down to 50 nm. The photostability and high luminance of QD evidently improve the signal-to-noise ratio and reproducibility of near-field optical data. Importantly, the blinking-intensity analysis was proposed to identify single QD, providing a calibration to relate intensity to numbers of antibody for the first time. Additionally, the fluorescence-topographic imaging enables us to investigate the topographic location pattern. Our results demonstrate that CD44 molecules on MSCs are enriched into nanosized domain and they predominantly locate on the peak of the membrane protrusions, which may contribute to clarify the underlying mechanism of functions ascribed to these molecules.
机译:膜蛋白和脂质结构域的横向组织对许多细胞过程都有直接的影响,但是通常这些结构域太小,无法通过荧光显微镜的衍射极限分辨率来分辨。在这里,我们使用基于近场光学成像的量子点(QD)标记,来研究空气中固定间充质干细胞(MSCs)的透明质酸受体CD44分子的纳米级组织,其光学分辨率低至50 nm。 QD的光稳定性和高亮度明显改善了近场光学数据的信噪比和可再现性。重要的是,提出了闪烁强度分析以鉴定单个QD,首次提供了将强度与抗体数量相关的校准方法。此外,荧光地形图成像使我们能够研究地形图的位置模式。我们的结果表明,MSCs上的CD44分子富集到纳米域中,并且主要位于膜突起的峰上,这可能有助于阐明归因于这些分子的潜在机制。

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