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Simple method for sub-diffraction resolution imaging of cellular structures on standard confocal microscopes by three-photon absorption of quantum dots.

机译:通过共聚焦显微镜的三光子吸收,在标准共聚焦显微镜上对细胞结构进行亚衍射分辨率成像的简单方法。

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摘要

This study describes a simple technique that improves a recently developed 3D sub-diffraction imaging method based on three-photon absorption of commercially available quantum dots. The method combines imaging of biological samples via tri-exciton generation in quantum dots with deconvolution and spectral multiplexing, resulting in a novel approach for multi-color imaging of even thick biological samples at a 1.4 to 1.9-fold better spatial resolution. This approach is realized on a conventional confocal microscope equipped with standard continuous-wave lasers. We demonstrate the potential of multi-color tri-exciton imaging of quantum dots combined with deconvolution on viral vesicles in lentivirally transduced cells as well as intermediate filaments in three-dimensional clusters of mouse-derived neural stem cells (neurospheres) and dense microtubuli arrays in myotubes formed by stacks of differentiated C2C12 myoblasts.
机译:这项研究描述了一种简单的技术,该技术改进了最近开发的基于市售量子点的三光子吸收的3D亚衍射成像方法。该方法结合了在量子点中通过三激子产生对生物样本进行的成像与去卷积和光谱多路复用,从而产生了一种新颖的方法,可以对厚的生物样本进行多色成像,其空间分辨率提高了1.4到1.9倍。这种方法是在配备有标准连续波激光器的常规共聚焦显微镜上实现的。我们证明了量子点的多色三激子成像与慢病毒转导细胞中的病毒小泡以及小鼠衍生的神经干细胞(神经球)和密集的微管阵列的三维簇中的中间细丝结合的反卷积的潜力由分化的C2C12成肌细胞堆叠形成的肌管。

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