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1.
Protein & Cell ; (12): 211-220, 2015.
Article in English | WPRIM | ID: wpr-757600

ABSTRACT

Super-resolution microscopy techniques have overcome the limit of optical diffraction. Recently, the Bayesian analysis of Bleaching and Blinking data (3B) method has emerged as an important tool to obtain super-resolution fluorescence images. 3B uses the change in information caused by adding or removing fluorophores in the cell to fit the data. When adding a new fluorophore, 3B selects a random initial position, optimizes this position and then determines its reliability. However, the fluorophores are not evenly distributed in the entire image region, and the fluorescence intensity at a given position positively correlates with the probability of observing a fluorophore at this position. In this paper, we present a Bayesian analysis of Bleaching and Blinking microscopy method based on fluorescence intensity distribution (FID3B). We utilize the intensity distribution to select more reliable positions as the initial positions of fluorophores. This approach can improve the reconstruction results and significantly reduce the computational time. We validate the performance of our method using both simulated data and experimental data from cellular structures. The results confirm the effectiveness of our method.


Subject(s)
Animals , Bayes Theorem , COS Cells , Chlorocebus aethiops , Computer Simulation , Green Fluorescent Proteins , Metabolism , Microscopy, Fluorescence , Methods , Molecular Imaging , Methods
2.
Protein & Cell ; (12): 598-606, 2013.
Article in English | WPRIM | ID: wpr-757785

ABSTRACT

The resolution of single molecule localization imaging techniques largely depends on the precision of localization algorithms. However, the commonly used Gaussian function is not appropriate for anisotropic dipoles because it is not the true point spread function. We derived the theoretical point spread function of tilted dipoles with restricted mobility and developed an algorithm based on an artificial neural network for estimating the localization, orientation and mobility of individual dipoles. Compared with fitting-based methods, our algorithm demonstrated ultrafast speed and higher accuracy, reduced sensitivity to defocusing, strong robustness and adaptability, making it an optimal choice for both two-dimensional and three-dimensional super-resolution imaging analysis.


Subject(s)
Animals , Humans , Alcohol Oxidoreductases , Genetics , Metabolism , Algorithms , COS Cells , Chlorocebus aethiops , Cytochrome P-450 Enzyme System , Genetics , Metabolism , HeLa Cells , Imaging, Three-Dimensional , Microscopy, Fluorescence , Normal Distribution , Plasmids , Metabolism
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