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Multi-color quantum dot stochastic optical reconstruction microscopy (qSTORM)

机译:多色量子点随机光学重建显微镜(qSTORM)

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Although Single Molecule Localization (SML) techniques have pushed the resolution of fluorescence microscopy beyond the diffraction limit, the accuracy of SML has been limited by the brightness of the fluorophores. The introduction of Quantum Dots (QD) for SML promises to overcome this barrier, and the QD Blueing technique provides a novel approach to SML microscopy. QDs have a higher quantum yield and absorption cross-section, making them brighter, thereby providing a higher accuracy of localization. The blueing technique is also faster and more quantitative than other SML techniques such as dSTORM. The initial bleaching step required by dSTORM is not necessary and each QD is imaged only once as its emission spectrum moves through the blueing window in contrast to dSTORM where the same molecule might be imaged multiple times. Single color QD Blueing has been demonstrated. However in biological imaging, multi-color imaging is essential for understanding the samples under study. Here we introduce two color super-resolution microscopy using QD Blueing on biological samples. We demonstrate simultaneous imaging of microtubules and mitochondria in HepG2 cells with a localization accuracy of 40nm. We further show how QD Blueing can be optimized through the control of the sample mounting medium.
机译:尽管单分子定位(SML)技术已将荧光显微镜的分辨率推到了衍射极限之外,但SML的准确性受到荧光团亮度的限制。用于SML的量子点(QD)的引入有望克服这一障碍,而QD蓝化技术为SML显微镜提供了一种新颖的方法。量子点具有更高的量子产率和吸收截面,使其更亮,从而提供更高的定位精度。与其他SML技术(例如dSTORM)相比,蓝化技术也更快,更定量。 dSTORM不需要初始的漂白步骤,并且每个QD的发射光谱穿过蓝色窗口时仅成像一次,而dSTORM则可能对同一分子进行多次成像。已证明单色QD蓝变。但是,在生物成像中,多色成像对于了解正在研究的样品至关重要。在这里,我们介绍对生物样品使用QD蓝化的两种颜色的超分辨率显微镜。我们展示了HepG2细胞中的微管和线粒体的同步成像,定位精度为40nm。我们进一步展示了如何通过样品安装介质的控制来优化QD Blueing。

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