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The role of electron irradiation history in liquid cell transmission electron microscopy
In situ liquid cell transmission electron microscopy (LC-TEM) allows dynamic nanoscale characterization of systems in a hydrated state. Although powerful, this technique remains impaired by issues of repeatability that limit experimental fidelity and hinder the identification and control of some var...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930397/ https://www.ncbi.nlm.nih.gov/pubmed/29725619 http://dx.doi.org/10.1126/sciadv.aaq1202 |
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author | Moser, Trevor H. Mehta, Hardeep Park, Chiwoo Kelly, Ryan T. Shokuhfar, Tolou Evans, James E. |
author_facet | Moser, Trevor H. Mehta, Hardeep Park, Chiwoo Kelly, Ryan T. Shokuhfar, Tolou Evans, James E. |
author_sort | Moser, Trevor H. |
collection | PubMed |
description | In situ liquid cell transmission electron microscopy (LC-TEM) allows dynamic nanoscale characterization of systems in a hydrated state. Although powerful, this technique remains impaired by issues of repeatability that limit experimental fidelity and hinder the identification and control of some variables underlying observed dynamics. We detail new LC-TEM devices that improve experimental reproducibility by expanding available imaging area and providing a platform for investigating electron flux history on the sample. Irradiation history is an important factor influencing LC-TEM results that has, to this point, been largely qualitatively and not quantitatively described. We use these devices to highlight the role of cumulative electron flux history on samples from both nanoparticle growth and biological imaging experiments and demonstrate capture of time zero, low-dose images on beam-sensitive samples. In particular, the ability to capture pristine images of biological samples, where the acquired image is the first time that the cell experiences significant electron flux, allowed us to determine that nanoparticle movement compared to the cell membrane was a function of cell damage and therefore an artifact rather than visualizing cell dynamics in action. These results highlight just a subset of the new science that is accessible with LC-TEM through the new multiwindow devices with patterned focusing aides. |
format | Online Article Text |
id | pubmed-5930397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59303972018-05-03 The role of electron irradiation history in liquid cell transmission electron microscopy Moser, Trevor H. Mehta, Hardeep Park, Chiwoo Kelly, Ryan T. Shokuhfar, Tolou Evans, James E. Sci Adv Research Articles In situ liquid cell transmission electron microscopy (LC-TEM) allows dynamic nanoscale characterization of systems in a hydrated state. Although powerful, this technique remains impaired by issues of repeatability that limit experimental fidelity and hinder the identification and control of some variables underlying observed dynamics. We detail new LC-TEM devices that improve experimental reproducibility by expanding available imaging area and providing a platform for investigating electron flux history on the sample. Irradiation history is an important factor influencing LC-TEM results that has, to this point, been largely qualitatively and not quantitatively described. We use these devices to highlight the role of cumulative electron flux history on samples from both nanoparticle growth and biological imaging experiments and demonstrate capture of time zero, low-dose images on beam-sensitive samples. In particular, the ability to capture pristine images of biological samples, where the acquired image is the first time that the cell experiences significant electron flux, allowed us to determine that nanoparticle movement compared to the cell membrane was a function of cell damage and therefore an artifact rather than visualizing cell dynamics in action. These results highlight just a subset of the new science that is accessible with LC-TEM through the new multiwindow devices with patterned focusing aides. American Association for the Advancement of Science 2018-04-20 /pmc/articles/PMC5930397/ /pubmed/29725619 http://dx.doi.org/10.1126/sciadv.aaq1202 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Moser, Trevor H. Mehta, Hardeep Park, Chiwoo Kelly, Ryan T. Shokuhfar, Tolou Evans, James E. The role of electron irradiation history in liquid cell transmission electron microscopy |
title | The role of electron irradiation history in liquid cell transmission electron microscopy |
title_full | The role of electron irradiation history in liquid cell transmission electron microscopy |
title_fullStr | The role of electron irradiation history in liquid cell transmission electron microscopy |
title_full_unstemmed | The role of electron irradiation history in liquid cell transmission electron microscopy |
title_short | The role of electron irradiation history in liquid cell transmission electron microscopy |
title_sort | role of electron irradiation history in liquid cell transmission electron microscopy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930397/ https://www.ncbi.nlm.nih.gov/pubmed/29725619 http://dx.doi.org/10.1126/sciadv.aaq1202 |
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