Abstract

Conventional analysis of fluorescence recovery after photobleaching (FRAP) data for diffusion coefficient estimation typically involves fitting an analytical or numerical FRAP model to the recovery curve data using non‐linear least squares. Depending on the model, this can be time consuming, especially for batch analysis of large numbers of data sets and if multiple initial guesses for the parameter vector are used to ensure convergence. In this work, we develop a completely new approach, DeepFRAP, utilizing machine learning for parameter estimation in FRAP. From a numerical FRAP model developed in previous work, we generate a very large set of simulated recovery curve data with realistic noise levels. The data are used for training different deep neural network regression models for prediction of several parameters, most importantly the diffusion coefficient. The neural networks are extremely fast and can estimate the parameters orders of magnitude faster than least squares. The performance of the neural network estimation framework is compared to conventional least squares estimation on simulated data, and found to be strikingly similar. Also, a simple experimental validation is performed, demonstrating excellent agreement between the two methods. We make the data and code used publicly available to facilitate further development of machine learning‐based estimation in FRAP.Lay descriptionFluorescence recovery after photobleaching (FRAP) is one of the most frequently used methods for microscopy‐based diffusion measurements and broadly used in materials science, pharmaceutics, food science and cell biology. In a FRAP experiment, a laser is used to photobleach fluorescent particles in a region. By analysing the recovery of the fluorescence intensity due to the diffusion of still fluorescent particles, the diffusion coefficient and other parameters can be estimated. Typically, a confocal laser scanning microscope (CLSM) is used to image the time evolution of the recovery, and a model is fit using least squares to obtain parameter estimates. In this work, we introduce a new, fast and accurate method for analysis of data from FRAP. The new method is based on using artificial neural networks to predict parameter values, such as the diffusion coefficient, effectively circumventing classical least squares fitting. This leads to a dramatic speed‐up, especially noticeable when analysing large numbers of FRAP data sets, while still producing results in excellent agreement with least squares. Further, the neural network estimates can be used as very good initial guesses for least squares estimation in order to make the least squares optimization convergence much faster than it otherwise would. This provides for obtaining, for example, diffusion coefficients as soon as possible, spending minimal time on data analysis. In this fashion, the proposed method facilitates efficient use of the experimentalist's time which is the main motivation to our approach. The concept is demonstrated on pure diffusion. However, the concept can easily be extended to the diffusion and binding case. The concept is likely to be useful in all application areas of FRAP, including diffusion in cells, gels and solutions.

Highlights

  • Fluorescence recovery after photobleaching (FRAP) is a powerful technique for characterization of different diffusion processes and is used on a regular basis in materials science, pharmaceutics, food science and cell biology.[1]

  • We develop a completely new approach for FRAP analysis based on machine learning for parameter estimation, that we refer to as DeepFRAP

  • Using the numerical FRAP model developed in Ref. 35, we generate a very large set of simulated recovery curves with realistic noise levels covering a broad range of diffusion coefficients, image intensities, amounts of bleaching and noise levels

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Summary

Introduction

Fluorescence recovery after photobleaching (FRAP) is a powerful technique for characterization of different diffusion processes and is used on a regular basis in materials science, pharmaceutics, food science and cell biology.[1]. In a typical FRAP experiment, fluorescent particles are photobleached by a high-intensity laser in a bleach region ( referred to as region of interest, ROI) that is typically either circular or rectangular. Unbleached particles will move into the bleach region, leading to a recovery of the fluorescence intensity within the bleach region. Under the assumption that all particles are mobile and that the fraction of bleached particles in the whole sample is negligible, the fluorescence will eventually recover to the prebleach intensity. In most FRAP experiments today, a confocal laser scanning microscope (CLSM) is used to image the time evolution of the recovery, using a far lower laser intensity for the imaging than for the bleaching. Quantitative information is obtained by fitting a model for the fluorescence intensity as a function of time, and possibly of space, to the experimental data

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