Improving 3D MA-TIRF Reconstruction with Deconvolution and Background Estimation

Emmanuel Soubies, L. Blanc-Féraud, S. Schaub, E. Obberghen-Schilling
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引用次数: 2

Abstract

Total internal reflection fluorescence microscopy (TIRF) produces 2D images of the fluorescent activity integrated over a very thin layer adjacent to the glass coverslip. By varying the illumination angle (multi-angle TIRF), a stack of 2D images is acquired from which it is possible to estimate the axial position of the observed biological structures. Due to its unique optical sectioning capability, this technique is ideal to observe and study biological processes at the vicinity of the cell membrane. In this paper, we propose an efficient reconstruction algorithm for multi-angle TIRF microscopy which accounts for both the PSF of the acquisition system (diffraction) and the background signal (e.g., autofluorescence). It jointly performs volume reconstruction, deconvolution, and background estimation. This algorithm, based on the simultaneous-direction method of multipliers (SDMM), relies on a suitable splitting of the optimization problem which allows to obtain closed form solutions at each step of the algorithm. Finally, numerical experiments reveal the importance of considering the background signal into the reconstruction process, which reinforces the relevance of the proposed approach.
基于反卷积和背景估计的三维MA-TIRF重建方法
全内反射荧光显微镜(TIRF)产生二维图像的荧光活性集成在一个非常薄的层相邻的玻璃盖。通过改变照明角度(多角度TIRF),可以获得一堆二维图像,从中可以估计观察到的生物结构的轴向位置。由于其独特的光学切片能力,该技术非常适合观察和研究细胞膜附近的生物过程。在本文中,我们提出了一种高效的多角度TIRF显微镜重建算法,该算法同时考虑了采集系统的PSF(衍射)和背景信号(如自体荧光)。它联合进行体积重建、反褶积和背景估计。该算法基于同时方向乘法器方法(SDMM),依赖于优化问题的适当拆分,使得算法的每一步都能得到封闭形式的解。最后,数值实验揭示了在重建过程中考虑背景信号的重要性,从而增强了所提方法的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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