Literature DB >> 21354390

Are assumptions about the model type necessary in reaction-diffusion modeling? A FRAP application.

Juliane Mai1, Saskia Trump, Rizwan Ali, R Louis Schiltz, Gordon Hager, Thomas Hanke, Irina Lehmann, Sabine Attinger.   

Abstract

At present, fluorescence recovery after photobleaching (FRAP) data are interpreted using various types of reaction-diffusion (RD) models: the model type is usually fixed first, and corresponding model parameters are inferred subsequently. In this article, we describe what we believe to be a novel approach for RD modeling without using any assumptions of model type or parameters. To the best of our knowledge, this is the first attempt to address both model-type and parameter uncertainties in inverting FRAP data. We start from the most general RD model, which accounts for a flexible number of molecular fractions, all mobile, with different diffusion coefficients. The maximal number of possible binding partners is identified and optimal parameter sets for these models are determined in a global search of the parameter-space using the Simulated Annealing strategy. The numerical performance of the described techniques was assessed using artificial and experimental FRAP data. Our general RD model outperformed the standard RD models used previously in modeling FRAP measurements and showed that intracellular molecular mobility can only be described adequately by allowing for multiple RD processes. Therefore, it is important to search not only for the optimal parameter set but also for the optimal model type.
Copyright © 2011 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Mesh:

Year:  2011        PMID: 21354390      PMCID: PMC3043225          DOI: 10.1016/j.bpj.2011.01.041

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  38 in total

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Journal:  Mol Pharmacol       Date:  1997-08       Impact factor: 4.436

3.  Fluorescence recovery after photobleaching (FRAP) methods for visualizing protein dynamics in living mammalian cell nuclei.

Authors:  Diana A Stavreva; James G McNally
Journal:  Methods Enzymol       Date:  2004       Impact factor: 1.600

4.  A class of exact solutions for biomacromolecule diffusion-reaction in live cells.

Authors:  Kouroush Sadegh Zadeh; Hubert J Montas
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5.  Analysis of binding at a single spatially localized cluster of binding sites by fluorescence recovery after photobleaching.

Authors:  Brian L Sprague; Florian Müller; Robert L Pego; Peter M Bungay; Diana A Stavreva; James G McNally
Journal:  Biophys J       Date:  2006-05-05       Impact factor: 4.033

6.  A reaction-diffusion model to study RNA motion by quantitative fluorescence recovery after photobleaching.

Authors:  José Braga; James G McNally; Maria Carmo-Fonseca
Journal:  Biophys J       Date:  2007-01-26       Impact factor: 4.033

7.  Protein mobility in the cytoplasm of Escherichia coli.

Authors:  M B Elowitz; M G Surette; P E Wolf; J B Stock; S Leibler
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8.  Theoretical analysis of fluorescence photobleaching recovery experiments.

Authors:  D M Soumpasis
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  6 in total

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Authors:  Juliane Mai; Saskia Trump; Irina Lehmann; Sabine Attinger
Journal:  Biophys J       Date:  2013-05-07       Impact factor: 4.033

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Authors:  Patrick M Boyle; Jinzhu Yu; Aleksandra Klimas; John C Williams; Natalia A Trayanova; Emilia Entcheva
Journal:  Sci Rep       Date:  2021-04-29       Impact factor: 4.996

5.  Dissection of cell cycle-dependent dynamics of Dnmt1 by FRAP and diffusion-coupled modeling.

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Journal:  Nucleic Acids Res       Date:  2013-03-27       Impact factor: 16.971

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  6 in total

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