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Automatic detection of diffusion modes within biological membranes using back-propagation neural network

BACKGROUND: Single particle tracking (SPT) is nowadays one of the most popular technique to probe spatio-temporal dynamics of proteins diffusing within the plasma membrane. Indeed membrane components of eukaryotic cells are very dynamic molecules and can diffuse according to different motion modes....

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Autores principales: Dosset, Patrice, Rassam, Patrice, Fernandez, Laurent, Espenel, Cedric, Rubinstein, Eric, Margeat, Emmanuel, Milhiet, Pierre-Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855490/
https://www.ncbi.nlm.nih.gov/pubmed/27141816
http://dx.doi.org/10.1186/s12859-016-1064-z
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author Dosset, Patrice
Rassam, Patrice
Fernandez, Laurent
Espenel, Cedric
Rubinstein, Eric
Margeat, Emmanuel
Milhiet, Pierre-Emmanuel
author_facet Dosset, Patrice
Rassam, Patrice
Fernandez, Laurent
Espenel, Cedric
Rubinstein, Eric
Margeat, Emmanuel
Milhiet, Pierre-Emmanuel
author_sort Dosset, Patrice
collection PubMed
description BACKGROUND: Single particle tracking (SPT) is nowadays one of the most popular technique to probe spatio-temporal dynamics of proteins diffusing within the plasma membrane. Indeed membrane components of eukaryotic cells are very dynamic molecules and can diffuse according to different motion modes. Trajectories are often reconstructed frame-by-frame and dynamic properties often evaluated using mean square displacement (MSD) analysis. However, to get statistically significant results in tracking experiments, analysis of a large number of trajectories is required and new methods facilitating this analysis are still needed. RESULTS: In this study we developed a new algorithm based on back-propagation neural network (BPNN) and MSD analysis using a sliding window. The neural network was trained and cross validated with short synthetic trajectories. For simulated and experimental data, the algorithm was shown to accurately discriminate between Brownian, confined and directed diffusion modes within one trajectory, the 3 main of diffusion encountered for proteins diffusing within biological membranes. It does not require a minimum number of observed particle displacements within the trajectory to infer the presence of multiple motion states. The size of the sliding window was small enough to measure local behavior and to detect switches between different diffusion modes for segments as short as 20 frames. It also provides quantitative information from each segment of these trajectories. Besides its ability to detect switches between 3 modes of diffusion, this algorithm is able to analyze simultaneously hundreds of trajectories with a short computational time. CONCLUSION: This new algorithm, implemented in powerful and handy software, provides a new conceptual and versatile tool, to accurately analyze the dynamic behavior of membrane components. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1064-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-48554902016-05-16 Automatic detection of diffusion modes within biological membranes using back-propagation neural network Dosset, Patrice Rassam, Patrice Fernandez, Laurent Espenel, Cedric Rubinstein, Eric Margeat, Emmanuel Milhiet, Pierre-Emmanuel BMC Bioinformatics Research Article BACKGROUND: Single particle tracking (SPT) is nowadays one of the most popular technique to probe spatio-temporal dynamics of proteins diffusing within the plasma membrane. Indeed membrane components of eukaryotic cells are very dynamic molecules and can diffuse according to different motion modes. Trajectories are often reconstructed frame-by-frame and dynamic properties often evaluated using mean square displacement (MSD) analysis. However, to get statistically significant results in tracking experiments, analysis of a large number of trajectories is required and new methods facilitating this analysis are still needed. RESULTS: In this study we developed a new algorithm based on back-propagation neural network (BPNN) and MSD analysis using a sliding window. The neural network was trained and cross validated with short synthetic trajectories. For simulated and experimental data, the algorithm was shown to accurately discriminate between Brownian, confined and directed diffusion modes within one trajectory, the 3 main of diffusion encountered for proteins diffusing within biological membranes. It does not require a minimum number of observed particle displacements within the trajectory to infer the presence of multiple motion states. The size of the sliding window was small enough to measure local behavior and to detect switches between different diffusion modes for segments as short as 20 frames. It also provides quantitative information from each segment of these trajectories. Besides its ability to detect switches between 3 modes of diffusion, this algorithm is able to analyze simultaneously hundreds of trajectories with a short computational time. CONCLUSION: This new algorithm, implemented in powerful and handy software, provides a new conceptual and versatile tool, to accurately analyze the dynamic behavior of membrane components. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1064-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-04 /pmc/articles/PMC4855490/ /pubmed/27141816 http://dx.doi.org/10.1186/s12859-016-1064-z Text en © Dosset et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Dosset, Patrice
Rassam, Patrice
Fernandez, Laurent
Espenel, Cedric
Rubinstein, Eric
Margeat, Emmanuel
Milhiet, Pierre-Emmanuel
Automatic detection of diffusion modes within biological membranes using back-propagation neural network
title Automatic detection of diffusion modes within biological membranes using back-propagation neural network
title_full Automatic detection of diffusion modes within biological membranes using back-propagation neural network
title_fullStr Automatic detection of diffusion modes within biological membranes using back-propagation neural network
title_full_unstemmed Automatic detection of diffusion modes within biological membranes using back-propagation neural network
title_short Automatic detection of diffusion modes within biological membranes using back-propagation neural network
title_sort automatic detection of diffusion modes within biological membranes using back-propagation neural network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855490/
https://www.ncbi.nlm.nih.gov/pubmed/27141816
http://dx.doi.org/10.1186/s12859-016-1064-z
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