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通过二维空间对交叉相关可视化活细胞中分子扩散的屏障和障碍。

Visualization of barriers and obstacles to molecular diffusion in live cells by spatial pair-cross-correlation in two dimensions.

作者信息

Malacrida Leonel, Hedde Per Niklas, Ranjit Suman, Cardarelli Francesco, Gratton Enrico

机构信息

Laboratory for Fluorescence Dynamics, Department of Biomedical Engineering, University of California, Irvine, USA.

Área de Investigación Respiratoria, Departamento de Fisiopatología, Hospital de Clínicas, Facultad de Medicina, Universidad de la República, Uruguay.

出版信息

Biomed Opt Express. 2017 Dec 20;9(1):303-321. doi: 10.1364/BOE.9.000303. eCollection 2018 Jan 1.

Abstract

Despite recent advances in optical super-resolution, we lack a method that can visualize the path followed by diffusing molecules in the cytoplasm or in the nucleus of cells. Fluorescence correlation spectroscopy (FCS) provides molecular dynamics at the single molecule level by averaging the behavior of many molecules over time at a single spot, thus achieving very good statistics but at only one point in the cell. Earlier image-based methods including raster-scan and spatiotemporal image correlation need spatial averaging over relatively large areas, thus compromising spatial resolution. Here, we use spatial pair-cross-correlation in two dimensions (2D-pCF) to obtain relatively high resolution images of molecular diffusion dynamics and transport in live cells. The 2D-pCF method measures the time for a particle to go from one location to another by cross-correlating the intensity fluctuations at specific points in an image. Hence, a visual map of the average path followed by molecules is created.

摘要

尽管光学超分辨率技术最近取得了进展,但我们仍缺乏一种能够可视化扩散分子在细胞质或细胞核中所遵循路径的方法。荧光相关光谱法(FCS)通过在单个点上对许多分子随时间的行为进行平均,在单分子水平上提供分子动力学信息,从而获得非常好的统计数据,但仅在细胞中的一个点上。早期基于图像的方法,包括光栅扫描和时空图像相关性,需要在相对较大的区域进行空间平均,从而牺牲了空间分辨率。在这里,我们使用二维空间对交叉相关性(2D-pCF)来获得活细胞中分子扩散动力学和运输的相对高分辨率图像。2D-pCF方法通过对图像中特定点的强度波动进行交叉相关来测量粒子从一个位置移动到另一个位置的时间。因此,创建了分子所遵循的平均路径的可视化图谱。

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