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Visualization of molecular structures using HoloLens-based augmented reality

Biological molecules and biologically active small molecules are complex three dimensional structures. Current flat screen monitors are limited in their ability to convey the full three dimensional characteristics of these molecules. Augmented reality devices, including the Microsoft HoloLens, offer...

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Detalles Bibliográficos
Autores principales: Hoffman, MA, Provance, JB
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Informatics Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543343/
https://www.ncbi.nlm.nih.gov/pubmed/28815109
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author Hoffman, MA
Provance, JB
author_facet Hoffman, MA
Provance, JB
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description Biological molecules and biologically active small molecules are complex three dimensional structures. Current flat screen monitors are limited in their ability to convey the full three dimensional characteristics of these molecules. Augmented reality devices, including the Microsoft HoloLens, offer an immersive platform to change how we interact with molecular visualizations. We describe a process to incorporate the three dimensional structures of small molecules and complex proteins into the Microsoft HoloLens using aspirin and the human leukocyte antigen (HLA) as examples. Small molecular structures can be introduced into the HoloStudio application, which provides native support for rotating, resizing and performing other interactions with these molecules. Larger molecules can be imported through the Unity gaming development platform and then Microsoft Visual Developer. The processes described here can be modified to import a wide variety of molecular structures into augmented reality systems and improve our comprehension of complex structural features.
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spelling pubmed-55433432017-08-16 Visualization of molecular structures using HoloLens-based augmented reality Hoffman, MA Provance, JB AMIA Jt Summits Transl Sci Proc Articles Biological molecules and biologically active small molecules are complex three dimensional structures. Current flat screen monitors are limited in their ability to convey the full three dimensional characteristics of these molecules. Augmented reality devices, including the Microsoft HoloLens, offer an immersive platform to change how we interact with molecular visualizations. We describe a process to incorporate the three dimensional structures of small molecules and complex proteins into the Microsoft HoloLens using aspirin and the human leukocyte antigen (HLA) as examples. Small molecular structures can be introduced into the HoloStudio application, which provides native support for rotating, resizing and performing other interactions with these molecules. Larger molecules can be imported through the Unity gaming development platform and then Microsoft Visual Developer. The processes described here can be modified to import a wide variety of molecular structures into augmented reality systems and improve our comprehension of complex structural features. American Medical Informatics Association 2017-07-26 /pmc/articles/PMC5543343/ /pubmed/28815109 Text en ©2017 AMIA - All rights reserved. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose
spellingShingle Articles
Hoffman, MA
Provance, JB
Visualization of molecular structures using HoloLens-based augmented reality
title Visualization of molecular structures using HoloLens-based augmented reality
title_full Visualization of molecular structures using HoloLens-based augmented reality
title_fullStr Visualization of molecular structures using HoloLens-based augmented reality
title_full_unstemmed Visualization of molecular structures using HoloLens-based augmented reality
title_short Visualization of molecular structures using HoloLens-based augmented reality
title_sort visualization of molecular structures using hololens-based augmented reality
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543343/
https://www.ncbi.nlm.nih.gov/pubmed/28815109
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