BayesTICS:荧光成像中扩散稀疏估计的局部时间图像相关光谱和贝叶斯模拟技术

Biological imaging Pub Date : 2023-02-27 eCollection Date: 2023-01-01 DOI:10.1017/S2633903X23000041
Anca Caranfil, Yann Le Cunff, Charles Kervrann
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引用次数: 0

摘要

胞吐过程中囊泡的动力学和融合在细胞生物学中尚未得到很好的证实。一个悬而未决的问题是质膜上扩散过程的表征。全内反射荧光显微镜(TIRFM)已经成功地用于分析参与这一机制的蛋白质的协调。它能够以高帧率和合理的信噪比值捕获蛋白质的动态。然而,在细胞内单个扩散点的尺度上,可以分析和估计局部小区域扩散的方法学方法仍然缺乏。为了解决这个问题,我们提出了一种新的基于相关性的局部扩散估计方法。作为起点,我们考虑菲克第二扩散定律,它将扩散通量与浓度梯度联系起来。然后,我们推导了一个显式参数模型,该模型进一步拟合了从包含单个点的感兴趣区域(ROI)计算的时间相关信号。我们的建模和贝叶斯估计框架非常适合于表示孤立的扩散事件,并且对噪声、ROI大小和ROI中的点定位具有鲁棒性。BayesTICS的性能显示在合成和真实的TIRFM图像上,描绘了转铁蛋白受体蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BayesTICS: Local temporal image correlation spectroscopy and Bayesian simulation technique for sparse estimation of diffusion in fluorescence imaging.

The dynamics and fusion of vesicles during the last steps of exocytosis are not well established yet in cell biology. An open issue is the characterization of the diffusion process at the plasma membrane. Total internal reflection fluorescence microscopy (TIRFM) has been successfully used to analyze the coordination of proteins involved in this mechanism. It enables to capture dynamics of proteins with high frame rate and reasonable signal-to-noise values. Nevertheless, methodological approaches that can analyze and estimate diffusion in local small areas at the scale of a single diffusing spot within cells, are still lacking. To address this issue, we propose a novel correlation-based method for local diffusion estimation. As a starting point, we consider Fick's second law of diffusion that relates the diffusive flux to the gradient of the concentration. Then, we derive an explicit parametric model which is further fitted to time-correlation signals computed from regions of interest (ROI) containing individual spots. Our modeling and Bayesian estimation framework are well appropriate to represent isolated diffusion events and are robust to noise, ROI sizes, and localization of spots in ROIs. The performance of BayesTICS is shown on both synthetic and real TIRFM images depicting Transferrin Receptor proteins.

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