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Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation
This work seeks to remedy two deficiencies in the current nucleic acid nanotechnology software environment: the lack of both a fast and user-friendly visualization tool and a standard for structural analyses of simulated systems. We introduce here oxView, a web browser-based visualizer that can load...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337935/ https://www.ncbi.nlm.nih.gov/pubmed/32449920 http://dx.doi.org/10.1093/nar/gkaa417 |
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author | Poppleton, Erik Bohlin, Joakim Matthies, Michael Sharma, Shuchi Zhang, Fei Šulc, Petr |
author_facet | Poppleton, Erik Bohlin, Joakim Matthies, Michael Sharma, Shuchi Zhang, Fei Šulc, Petr |
author_sort | Poppleton, Erik |
collection | PubMed |
description | This work seeks to remedy two deficiencies in the current nucleic acid nanotechnology software environment: the lack of both a fast and user-friendly visualization tool and a standard for structural analyses of simulated systems. We introduce here oxView, a web browser-based visualizer that can load structures with over 1 million nucleotides, create videos from simulation trajectories, and allow users to perform basic edits to DNA and RNA designs. We additionally introduce open-source software tools for extracting common structural parameters to characterize large DNA/RNA nanostructures simulated using the coarse-grained modeling tool, oxDNA, which has grown in popularity in recent years and is frequently used to prototype new nucleic acid nanostructural designs, model biophysics of DNA/RNA processes, and rationalize experimental results. The newly introduced software tools facilitate the computational characterization of DNA/RNA designs by providing multiple analysis scripts, including mean structures and structure flexibility characterization, hydrogen bond fraying, and interduplex angles. The output of these tools can be loaded into oxView, allowing users to interact with the simulated structure in a 3D graphical environment and modify the structures to achieve the required properties. We demonstrate these newly developed tools by applying them to design and analysis of a range of DNA/RNA nanostructures. |
format | Online Article Text |
id | pubmed-7337935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73379352020-07-13 Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation Poppleton, Erik Bohlin, Joakim Matthies, Michael Sharma, Shuchi Zhang, Fei Šulc, Petr Nucleic Acids Res Methods Online This work seeks to remedy two deficiencies in the current nucleic acid nanotechnology software environment: the lack of both a fast and user-friendly visualization tool and a standard for structural analyses of simulated systems. We introduce here oxView, a web browser-based visualizer that can load structures with over 1 million nucleotides, create videos from simulation trajectories, and allow users to perform basic edits to DNA and RNA designs. We additionally introduce open-source software tools for extracting common structural parameters to characterize large DNA/RNA nanostructures simulated using the coarse-grained modeling tool, oxDNA, which has grown in popularity in recent years and is frequently used to prototype new nucleic acid nanostructural designs, model biophysics of DNA/RNA processes, and rationalize experimental results. The newly introduced software tools facilitate the computational characterization of DNA/RNA designs by providing multiple analysis scripts, including mean structures and structure flexibility characterization, hydrogen bond fraying, and interduplex angles. The output of these tools can be loaded into oxView, allowing users to interact with the simulated structure in a 3D graphical environment and modify the structures to achieve the required properties. We demonstrate these newly developed tools by applying them to design and analysis of a range of DNA/RNA nanostructures. Oxford University Press 2020-07-09 2020-05-25 /pmc/articles/PMC7337935/ /pubmed/32449920 http://dx.doi.org/10.1093/nar/gkaa417 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Poppleton, Erik Bohlin, Joakim Matthies, Michael Sharma, Shuchi Zhang, Fei Šulc, Petr Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation |
title | Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation |
title_full | Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation |
title_fullStr | Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation |
title_full_unstemmed | Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation |
title_short | Design, optimization and analysis of large DNA and RNA nanostructures through interactive visualization, editing and molecular simulation |
title_sort | design, optimization and analysis of large dna and rna nanostructures through interactive visualization, editing and molecular simulation |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337935/ https://www.ncbi.nlm.nih.gov/pubmed/32449920 http://dx.doi.org/10.1093/nar/gkaa417 |
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