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Light scattering microscopy measurements of single nuclei compared with GPU-accelerated FDTD simulations

机译:与GPU加速的FDTD仿真相比,单核的光散射显微镜测量

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摘要

Single cell nuclei were investigated using two-dimensional angularly and spectrally resolved scattering microscopy. We show that even for a qualitative comparison of experimental and theoretical data, the standard Mie model of a homogeneous sphere proves to be insufficient. Hence, an accelerated finite-difference time-domain method using a graphics processor unit and domain decomposition was implemented to analyze the experimental scattering patterns. The measured cell nuclei were modeled as single spheres with randomly distributed spherical inclusions of different size and refractive index representing the nucleoli and clumps of chromatin. Taking into account the nuclear heterogeneity of a large number of inclusions yields a qualitative agreement between experimental and theoretical spectra and illustrates the impact of the nuclear micro- and nanostructure on the scattering patterns.
机译:使用二维角度和光谱分辨散射显微镜研究单细胞核。我们表明,即使对实验和理论数据进行定性比较,均质球的标准Mie模型也被证明是不足的。因此,实现了使用图形处理器单元和域分解的加速有限差分时域方法,以分析实验散射图案。测得的细胞核被建模为单个球体,具有随机分布的球形包裹体,其大小和折射率分别代表染色质的核仁和团块。考虑到大量夹杂物的核不均一性,在实验光谱和理论光谱之间产生了定性一致性,并说明了核微结构和纳米结构对散射图的影响。

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