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3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries

Recent advances in electron microscopy have enabled the imaging of single cells in 3D at nanometer length scale resolutions. An uncharted frontier for in silico biology is the ability to simulate cellular processes using these observed geometries. Enabling such simulations requires watertight meshin...

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Autores principales: Lee, Christopher T., Laughlin, Justin G., Angliviel de La Beaumelle, Nils, Amaro, Rommie E., McCammon, J. Andrew, Ramamoorthi, Ravi, Holst, Michael, Rangamani, Padmini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162555/
https://www.ncbi.nlm.nih.gov/pubmed/32251448
http://dx.doi.org/10.1371/journal.pcbi.1007756
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author Lee, Christopher T.
Laughlin, Justin G.
Angliviel de La Beaumelle, Nils
Amaro, Rommie E.
McCammon, J. Andrew
Ramamoorthi, Ravi
Holst, Michael
Rangamani, Padmini
author_facet Lee, Christopher T.
Laughlin, Justin G.
Angliviel de La Beaumelle, Nils
Amaro, Rommie E.
McCammon, J. Andrew
Ramamoorthi, Ravi
Holst, Michael
Rangamani, Padmini
author_sort Lee, Christopher T.
collection PubMed
description Recent advances in electron microscopy have enabled the imaging of single cells in 3D at nanometer length scale resolutions. An uncharted frontier for in silico biology is the ability to simulate cellular processes using these observed geometries. Enabling such simulations requires watertight meshing of electron micrograph images into 3D volume meshes, which can then form the basis of computer simulations of such processes using numerical techniques such as the finite element method. In this paper, we describe the use of our recently rewritten mesh processing software, GAMer 2, to bridge the gap between poorly conditioned meshes generated from segmented micrographs and boundary marked tetrahedral meshes which are compatible with simulation. We demonstrate the application of a workflow using GAMer 2 to a series of electron micrographs of neuronal dendrite morphology explored at three different length scales and show that the resulting meshes are suitable for finite element simulations. This work is an important step towards making physical simulations of biological processes in realistic geometries routine. Innovations in algorithms to reconstruct and simulate cellular length scale phenomena based on emerging structural data will enable realistic physical models and advance discovery at the interface of geometry and cellular processes. We posit that a new frontier at the intersection of computational technologies and single cell biology is now open.
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spelling pubmed-71625552020-04-24 3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries Lee, Christopher T. Laughlin, Justin G. Angliviel de La Beaumelle, Nils Amaro, Rommie E. McCammon, J. Andrew Ramamoorthi, Ravi Holst, Michael Rangamani, Padmini PLoS Comput Biol Research Article Recent advances in electron microscopy have enabled the imaging of single cells in 3D at nanometer length scale resolutions. An uncharted frontier for in silico biology is the ability to simulate cellular processes using these observed geometries. Enabling such simulations requires watertight meshing of electron micrograph images into 3D volume meshes, which can then form the basis of computer simulations of such processes using numerical techniques such as the finite element method. In this paper, we describe the use of our recently rewritten mesh processing software, GAMer 2, to bridge the gap between poorly conditioned meshes generated from segmented micrographs and boundary marked tetrahedral meshes which are compatible with simulation. We demonstrate the application of a workflow using GAMer 2 to a series of electron micrographs of neuronal dendrite morphology explored at three different length scales and show that the resulting meshes are suitable for finite element simulations. This work is an important step towards making physical simulations of biological processes in realistic geometries routine. Innovations in algorithms to reconstruct and simulate cellular length scale phenomena based on emerging structural data will enable realistic physical models and advance discovery at the interface of geometry and cellular processes. We posit that a new frontier at the intersection of computational technologies and single cell biology is now open. Public Library of Science 2020-04-06 /pmc/articles/PMC7162555/ /pubmed/32251448 http://dx.doi.org/10.1371/journal.pcbi.1007756 Text en © 2020 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lee, Christopher T.
Laughlin, Justin G.
Angliviel de La Beaumelle, Nils
Amaro, Rommie E.
McCammon, J. Andrew
Ramamoorthi, Ravi
Holst, Michael
Rangamani, Padmini
3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries
title 3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries
title_full 3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries
title_fullStr 3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries
title_full_unstemmed 3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries
title_short 3D mesh processing using GAMer 2 to enable reaction-diffusion simulations in realistic cellular geometries
title_sort 3d mesh processing using gamer 2 to enable reaction-diffusion simulations in realistic cellular geometries
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162555/
https://www.ncbi.nlm.nih.gov/pubmed/32251448
http://dx.doi.org/10.1371/journal.pcbi.1007756
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