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Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature

Although structures of vitrified supramolecular complexes have been determined at near-atomic resolution, elucidating in situ molecular structure in living cells remains a challenge. Here, we report a straightforward liquid cell technique, originally developed for real-time visualization of dynamics...

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Autores principales: Kong, Lingli, Liu, Jianfang, Zhang, Meng, Lu, Zhuoyang, Xue, Han, Ren, Amy, Liu, Jiankang, Li, Jinping, Ling, Wai Li, Ren, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499825/
https://www.ncbi.nlm.nih.gov/pubmed/37704637
http://dx.doi.org/10.1038/s41467-023-41266-x
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author Kong, Lingli
Liu, Jianfang
Zhang, Meng
Lu, Zhuoyang
Xue, Han
Ren, Amy
Liu, Jiankang
Li, Jinping
Ling, Wai Li
Ren, Gang
author_facet Kong, Lingli
Liu, Jianfang
Zhang, Meng
Lu, Zhuoyang
Xue, Han
Ren, Amy
Liu, Jiankang
Li, Jinping
Ling, Wai Li
Ren, Gang
author_sort Kong, Lingli
collection PubMed
description Although structures of vitrified supramolecular complexes have been determined at near-atomic resolution, elucidating in situ molecular structure in living cells remains a challenge. Here, we report a straightforward liquid cell technique, originally developed for real-time visualization of dynamics at a liquid-gas interface using transmission electron microscopy, to image wet biological samples. Due to the scattering effects from the liquid phase, the micrographs display an amplitude contrast comparable to that observed in negatively stained samples. We succeed in resolving subunits within the protein complex GroEL imaged in a buffer solution at room temperature. Additionally, we capture various stages of virus cell entry, a process for which only sparse structural data exists due to their transient nature. To scrutinize the morphological details further, we used individual particle electron tomography for 3D reconstruction of each virus. These findings showcase this approach potential as an efficient, cost-effective complement to other microscopy technique in addressing biological questions at the molecular level.
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spelling pubmed-104998252023-09-15 Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature Kong, Lingli Liu, Jianfang Zhang, Meng Lu, Zhuoyang Xue, Han Ren, Amy Liu, Jiankang Li, Jinping Ling, Wai Li Ren, Gang Nat Commun Article Although structures of vitrified supramolecular complexes have been determined at near-atomic resolution, elucidating in situ molecular structure in living cells remains a challenge. Here, we report a straightforward liquid cell technique, originally developed for real-time visualization of dynamics at a liquid-gas interface using transmission electron microscopy, to image wet biological samples. Due to the scattering effects from the liquid phase, the micrographs display an amplitude contrast comparable to that observed in negatively stained samples. We succeed in resolving subunits within the protein complex GroEL imaged in a buffer solution at room temperature. Additionally, we capture various stages of virus cell entry, a process for which only sparse structural data exists due to their transient nature. To scrutinize the morphological details further, we used individual particle electron tomography for 3D reconstruction of each virus. These findings showcase this approach potential as an efficient, cost-effective complement to other microscopy technique in addressing biological questions at the molecular level. Nature Publishing Group UK 2023-09-13 /pmc/articles/PMC10499825/ /pubmed/37704637 http://dx.doi.org/10.1038/s41467-023-41266-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’ Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kong, Lingli
Liu, Jianfang
Zhang, Meng
Lu, Zhuoyang
Xue, Han
Ren, Amy
Liu, Jiankang
Li, Jinping
Ling, Wai Li
Ren, Gang
Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature
title Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature
title_full Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature
title_fullStr Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature
title_full_unstemmed Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature
title_short Facile hermetic TEM grid preparation for molecular imaging of hydrated biological samples at room temperature
title_sort facile hermetic tem grid preparation for molecular imaging of hydrated biological samples at room temperature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499825/
https://www.ncbi.nlm.nih.gov/pubmed/37704637
http://dx.doi.org/10.1038/s41467-023-41266-x
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