The role of electron irradiation history in liquid cell transmission electron microscopy

Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
American Association for the Advancement of Science (AAAS)
Published 2018
Publication Date:
2018-04-21
Publisher:
American Association for the Advancement of Science (AAAS)
Electronic ISSN:
2375-2548
Topics:
Natural Sciences in General
Published by:
_version_ 1836398905634324480
autor Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
beschreibung 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.
citation_standardnr 6242002
datenlieferant ipn_articles
feed_id 228416
feed_publisher American Association for the Advancement of Science (AAAS)
feed_publisher_url http://www.aaas.org/
insertion_date 2018-04-21
journaleissn 2375-2548
publikationsjahr_anzeige 2018
publikationsjahr_facette 2018
publikationsjahr_intervall 7984:2015-2019
publikationsjahr_sort 2018
publisher American Association for the Advancement of Science (AAAS)
quelle Science Advances
relation http://advances.sciencemag.org/cgi/content/short/4/4/eaaq1202?rss=1
search_space articles
shingle_author_1 Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
shingle_author_2 Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
shingle_author_3 Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
shingle_author_4 Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
shingle_catch_all_1 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 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.
Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
American Association for the Advancement of Science (AAAS)
2375-2548
23752548
shingle_catch_all_2 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 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.
Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
American Association for the Advancement of Science (AAAS)
2375-2548
23752548
shingle_catch_all_3 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 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.
Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
American Association for the Advancement of Science (AAAS)
2375-2548
23752548
shingle_catch_all_4 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 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.
Moser, T. H., Mehta, H., Park, C., Kelly, R. T., Shokuhfar, T., Evans, J. E.
American Association for the Advancement of Science (AAAS)
2375-2548
23752548
shingle_title_1 The role of electron irradiation history in liquid cell transmission electron microscopy
shingle_title_2 The role of electron irradiation history in liquid cell transmission electron microscopy
shingle_title_3 The role of electron irradiation history in liquid cell transmission electron microscopy
shingle_title_4 The role of electron irradiation history in liquid cell transmission electron microscopy
timestamp 2025-06-30T23:34:30.739Z
titel The role of electron irradiation history in liquid cell transmission electron microscopy
titel_suche The role of electron irradiation history in liquid cell transmission electron microscopy
topic TA-TD
uid ipn_articles_6242002