Inferring diffusion, reaction, and exchange parameters from imperfect FRAP
Enrico LorenzettiiD, Celia Municio-DiaziD, Nicolas MinciD, Arezki BoudaoudiD, Antoine FruleuxiD
Abstract
Fluorescence recovery after photobleaching (FRAP) is broadly used to investigate the dynamics of molecules in cells and tissues, notably to quantify diffusion coefficients. FRAP is based on the spatiotemporal imaging of fluorescent molecules following an initial bleaching of fluorescence in a region of the sample. Although a large number of methods have been developed to infer kinetic parameters from experiments, it is still a challenge to fully characterize molecular dynamics from noisy experiments in which diffusion is coupled to other molecular processes or in which the initial bleaching profile is not perfectly controlled. To address this challenge, we have developed HiFRAP to quantify the reaction-(or exchange-)diffusion kinetic parameters from FRAP under imperfect experimental conditions. HiFRAP is based on a low-rank approximation of a kernel related to the model Greens function and is implemented as an ImageJ/Python macro for (potentially curved) one-dimensional systems and for two-dimensional systems. To the best of our knowledge, HiFRAP offers features that have not been combined together: making no assumption on the initial bleaching profile, which does not need to be known; accounting for the limitation of the optical setup by diffraction; inferring several kinetic parameters from a single experiment; providing errors on parameter estimation; and testing model goodness. In the future, our approach could be applied to other dynamical processes described by linear partial differential equations, which could be useful beyond FRAP, in experiments where the concentration fields are monitored over space and time. SIGNIFICANCEFluorescence recovery after photobleaching (FRAP) is a microscopy approach that is widely used to investigate the diffusion and transport of molecules in life sciences and in material sciences. Numerous methods have been developed to derive kinetic parameters such as diffusion and binding coefficients. However, these methods suffer from limitations associated with experimental constraints, such as technical noise or an imperfectly known initial condition. To circumvent these limitations, we developed a comprehensive approach to estimate several kinetic parameters from a single experiment, to assess the precision of estimation, and to test whether the underlying model is well-suited. We implemented this approach in HiFRAP, an ImageJ/Python macro of broad applicability to one- and two-dimensional systems.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 3
- FWCI
- 1.13
- Field percentile
- top 24%
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Beyond analytic solution: analysis of FRAP experiments by spatial simulation of the forward problem
A. E. Cowan, L. M. Loew·bioRxiv·Mar 5, 2023
- Combined Selective Plane Illumination Microscopy and FRAP maps intranuclear diffusion of NLS-GFP
C. M. Hobson, E. T. O'Brien, … R. Superfine·Biophysical JournalPeer-reviewed·Aug 1, 2020
- Anomalous Diffusion Characterization by Fourier-Transform FRAP with Patterned Illumination
A. C. Geiger, C. J. Smith, … G. J. Simpson·bioRxiv·Mar 13, 2020
- ImpRes: A robust FRAP framework to quantify fast diffusion of cytoplasmic probes
Olivier Destrian, René‐Marc Mège, … Morgan Chabanon·bioRxiv·Aug 19, 2026
- Line-FRAP, a versatile method based on fluorescence recovery after photobleaching to measure diffusion rates in vitro and in vivo
D. Dey, S. Marciano, G. Schreiber·bioRxiv·Jul 1, 2020
- Experimental and simulated FRAP for the quantitative determination of protein diffusion in helical cells
Shariful Sakib, Cécile Fradin·Methods and Applications in FluorescencePeer-reviewed·Aug 18, 2026