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Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm

Understanding the relationship between intracellular motion and macromolecular structure remains a challenge in biology. Macromolecular structures are assembled from numerous molecules, some of which cannot be labeled. Most techniques to study motion require potentially cytotoxic dyes or transfectio...

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Autores principales: Gladstein, Scott, Almassalha, Luay M., Cherkezyan, Lusik, Chandler, John E., Eshein, Adam, Eid, Aya, Zhang, Di, Wu, Wenli, Bauer, Greta M., Stephens, Andrew D., Morochnik, Simona, Subramanian, Hariharan, Marko, John F., Ameer, Guillermo A., Szleifer, Igal, Backman, Vadim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458150/
https://www.ncbi.nlm.nih.gov/pubmed/30971691
http://dx.doi.org/10.1038/s41467-019-09717-6
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author Gladstein, Scott
Almassalha, Luay M.
Cherkezyan, Lusik
Chandler, John E.
Eshein, Adam
Eid, Aya
Zhang, Di
Wu, Wenli
Bauer, Greta M.
Stephens, Andrew D.
Morochnik, Simona
Subramanian, Hariharan
Marko, John F.
Ameer, Guillermo A.
Szleifer, Igal
Backman, Vadim
author_facet Gladstein, Scott
Almassalha, Luay M.
Cherkezyan, Lusik
Chandler, John E.
Eshein, Adam
Eid, Aya
Zhang, Di
Wu, Wenli
Bauer, Greta M.
Stephens, Andrew D.
Morochnik, Simona
Subramanian, Hariharan
Marko, John F.
Ameer, Guillermo A.
Szleifer, Igal
Backman, Vadim
author_sort Gladstein, Scott
collection PubMed
description Understanding the relationship between intracellular motion and macromolecular structure remains a challenge in biology. Macromolecular structures are assembled from numerous molecules, some of which cannot be labeled. Most techniques to study motion require potentially cytotoxic dyes or transfection, which can alter cellular behavior and are susceptible to photobleaching. Here we present a multimodal label-free imaging platform for measuring intracellular structure and macromolecular dynamics in living cells with a sensitivity to macromolecular structure as small as 20 nm and millisecond temporal resolution. We develop and validate a theory for temporal measurements of light interference. In vitro, we study how higher-order chromatin structure and dynamics change during cell differentiation and ultraviolet (UV) light irradiation. Finally, we discover cellular paroxysms, a near-instantaneous burst of macromolecular motion that occurs during UV induced cell death. With nanoscale sensitive, millisecond resolved capabilities, this platform could address critical questions about macromolecular behavior in live cells.
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spelling pubmed-64581502019-04-12 Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm Gladstein, Scott Almassalha, Luay M. Cherkezyan, Lusik Chandler, John E. Eshein, Adam Eid, Aya Zhang, Di Wu, Wenli Bauer, Greta M. Stephens, Andrew D. Morochnik, Simona Subramanian, Hariharan Marko, John F. Ameer, Guillermo A. Szleifer, Igal Backman, Vadim Nat Commun Article Understanding the relationship between intracellular motion and macromolecular structure remains a challenge in biology. Macromolecular structures are assembled from numerous molecules, some of which cannot be labeled. Most techniques to study motion require potentially cytotoxic dyes or transfection, which can alter cellular behavior and are susceptible to photobleaching. Here we present a multimodal label-free imaging platform for measuring intracellular structure and macromolecular dynamics in living cells with a sensitivity to macromolecular structure as small as 20 nm and millisecond temporal resolution. We develop and validate a theory for temporal measurements of light interference. In vitro, we study how higher-order chromatin structure and dynamics change during cell differentiation and ultraviolet (UV) light irradiation. Finally, we discover cellular paroxysms, a near-instantaneous burst of macromolecular motion that occurs during UV induced cell death. With nanoscale sensitive, millisecond resolved capabilities, this platform could address critical questions about macromolecular behavior in live cells. Nature Publishing Group UK 2019-04-10 /pmc/articles/PMC6458150/ /pubmed/30971691 http://dx.doi.org/10.1038/s41467-019-09717-6 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gladstein, Scott
Almassalha, Luay M.
Cherkezyan, Lusik
Chandler, John E.
Eshein, Adam
Eid, Aya
Zhang, Di
Wu, Wenli
Bauer, Greta M.
Stephens, Andrew D.
Morochnik, Simona
Subramanian, Hariharan
Marko, John F.
Ameer, Guillermo A.
Szleifer, Igal
Backman, Vadim
Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm
title Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm
title_full Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm
title_fullStr Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm
title_full_unstemmed Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm
title_short Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm
title_sort multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers uv induced cellular paroxysm
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458150/
https://www.ncbi.nlm.nih.gov/pubmed/30971691
http://dx.doi.org/10.1038/s41467-019-09717-6
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