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1.
Opt Express ; 23(13): 16866-83, 2015 Jun 29.
Artigo em Inglês | MEDLINE | ID: mdl-26191698

RESUMO

The computation of point spread functions, which are typically used to model the image profile of a single molecule, represents a central task in the analysis of single molecule microscopy data. To determine how the accuracy of the computation affects how well a single molecule can be localized, we investigate how the fineness with which the point spread function is integrated over an image pixel impacts the performance of the maximum likelihood location estimator. We consider both the Airy and the two-dimensional Gaussian point spread functions. Our results show that the point spread function needs to be adequately integrated over a pixel to ensure that the estimator closely recovers the true location of the single molecule with an accuracy that is comparable to the best possible accuracy as determined using the Fisher information formalism. Importantly, if integration with an insufficiently fine step size is carried out, the resulting estimates can be significantly different from the true location, particularly when the image data is acquired at relatively low magnifications. We also present a methodology for determining an adequate step size for integrating the point spread function.


Assuntos
Fenômenos Ópticos , Simulação por Computador , Imageamento Tridimensional , Funções Verossimilhança , Distribuição Normal
2.
PLoS One ; 10(7): e0134112, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26218251

RESUMO

The localization of fluorescent microspheres is often employed for drift correction and image registration in single molecule microscopy, and is commonly carried out by fitting a point spread function to the image of the given microsphere. The mismatch between the point spread function and the image of the microsphere, however, calls into question the suitability of this localization approach. To investigate this issue, we subject both simulated and experimental microsphere image data to a maximum likelihood estimator that localizes a microsphere by fitting an Airy pattern to its image, and assess the suitability of the approach by evaluating the ability of the estimator to recover the true location of the microsphere with the best possible accuracy as determined based on the Cramér-Rao lower bound. Assessing against criteria based on the standard errors of the mean and the variance for an ideal estimator of the microsphere's location, we find that microspheres up to 100 nm in diameter can in general be localized using a fixed width Airy pattern, and that microspheres as large as 1 µm in diameter can in general be localized using a floated width Airy pattern.


Assuntos
Algoritmos , Corantes Fluorescentes/química , Imageamento Tridimensional , Microscopia de Fluorescência/métodos , Microesferas , Fenômenos Ópticos , Simulação por Computador , Funções Verossimilhança , Nanotecnologia , Distribuição Normal , Processamento de Sinais Assistido por Computador , Razão Sinal-Ruído
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