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Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy

Analytical tools to study cell physiology are critical for optimizing drug-host interactions. Real time pulse chase NMR spectroscopy, RTPC-NMR, was introduced to monitor the kinetics of metabolite production in HEK 293T cells treated with COVID-19 vaccine-like lipid nanoparticles, LNPs, with and wit...

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Autores principales: Sciolino, Nicholas, Reverdatto, Sergey, Premo, Aaron, Breindel, Leonard, Yu, Jianchao, Theophall, Gregory, Burz, David S., Liu, Anna, Sulchek, Todd, Schmidt, Ann Marie, Ramasamy, Ravichandran, Shekhtman, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789524/
https://www.ncbi.nlm.nih.gov/pubmed/36566335
http://dx.doi.org/10.1038/s41598-022-26444-z
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author Sciolino, Nicholas
Reverdatto, Sergey
Premo, Aaron
Breindel, Leonard
Yu, Jianchao
Theophall, Gregory
Burz, David S.
Liu, Anna
Sulchek, Todd
Schmidt, Ann Marie
Ramasamy, Ravichandran
Shekhtman, Alexander
author_facet Sciolino, Nicholas
Reverdatto, Sergey
Premo, Aaron
Breindel, Leonard
Yu, Jianchao
Theophall, Gregory
Burz, David S.
Liu, Anna
Sulchek, Todd
Schmidt, Ann Marie
Ramasamy, Ravichandran
Shekhtman, Alexander
author_sort Sciolino, Nicholas
collection PubMed
description Analytical tools to study cell physiology are critical for optimizing drug-host interactions. Real time pulse chase NMR spectroscopy, RTPC-NMR, was introduced to monitor the kinetics of metabolite production in HEK 293T cells treated with COVID-19 vaccine-like lipid nanoparticles, LNPs, with and without mRNA. Kinetic flux parameters were resolved for the incorporation of isotopic label into metabolites and clearance of labeled metabolites from the cells. Changes in the characteristic times for alanine production implicated mitochondrial dysfunction as a consequence of treating the cells with lipid nanoparticles, LNPs. Mitochondrial dysfunction was largely abated by inclusion of mRNA in the LNPs, the presence of which increased the size and uniformity of the LNPs. The methodology is applicable to all cultured cells.
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spelling pubmed-97895242022-12-26 Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy Sciolino, Nicholas Reverdatto, Sergey Premo, Aaron Breindel, Leonard Yu, Jianchao Theophall, Gregory Burz, David S. Liu, Anna Sulchek, Todd Schmidt, Ann Marie Ramasamy, Ravichandran Shekhtman, Alexander Sci Rep Article Analytical tools to study cell physiology are critical for optimizing drug-host interactions. Real time pulse chase NMR spectroscopy, RTPC-NMR, was introduced to monitor the kinetics of metabolite production in HEK 293T cells treated with COVID-19 vaccine-like lipid nanoparticles, LNPs, with and without mRNA. Kinetic flux parameters were resolved for the incorporation of isotopic label into metabolites and clearance of labeled metabolites from the cells. Changes in the characteristic times for alanine production implicated mitochondrial dysfunction as a consequence of treating the cells with lipid nanoparticles, LNPs. Mitochondrial dysfunction was largely abated by inclusion of mRNA in the LNPs, the presence of which increased the size and uniformity of the LNPs. The methodology is applicable to all cultured cells. Nature Publishing Group UK 2022-12-24 /pmc/articles/PMC9789524/ /pubmed/36566335 http://dx.doi.org/10.1038/s41598-022-26444-z Text en © The Author(s) 2022 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's 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
Sciolino, Nicholas
Reverdatto, Sergey
Premo, Aaron
Breindel, Leonard
Yu, Jianchao
Theophall, Gregory
Burz, David S.
Liu, Anna
Sulchek, Todd
Schmidt, Ann Marie
Ramasamy, Ravichandran
Shekhtman, Alexander
Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy
title Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy
title_full Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy
title_fullStr Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy
title_full_unstemmed Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy
title_short Messenger RNA in lipid nanoparticles rescues HEK 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase NMR, RTPC-NMR, spectroscopy
title_sort messenger rna in lipid nanoparticles rescues hek 293 cells from lipid-induced mitochondrial dysfunction as studied by real time pulse chase nmr, rtpc-nmr, spectroscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789524/
https://www.ncbi.nlm.nih.gov/pubmed/36566335
http://dx.doi.org/10.1038/s41598-022-26444-z
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