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Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages

Protein synthesis, or mRNA translation, is the biological process through which genetic information stored in messenger RNAs is encoded into proteins. Here, we present an optimized protocol for assessing the translation rate in mouse adult microglia and cultured bone-marrow-derived macrophages. We d...

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Detalles Bibliográficos
Autores principales: Antignano, Ignazio, Keane, Lily, Capasso, Melania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509706/
https://www.ncbi.nlm.nih.gov/pubmed/37713309
http://dx.doi.org/10.1016/j.xpro.2023.102559
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author Antignano, Ignazio
Keane, Lily
Capasso, Melania
author_facet Antignano, Ignazio
Keane, Lily
Capasso, Melania
author_sort Antignano, Ignazio
collection PubMed
description Protein synthesis, or mRNA translation, is the biological process through which genetic information stored in messenger RNAs is encoded into proteins. Here, we present an optimized protocol for assessing the translation rate in mouse adult microglia and cultured bone-marrow-derived macrophages. We describe steps for isolating cells, treating them with a puromycin-analog probe, and fluorescently labeling the puromycylated-polypeptide chains. We then detail their quantification by flow cytometry or with a fluorescent plate reader. For complete details on the use and execution of this protocol, please refer to Keane et al. (2021).(1)
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spelling pubmed-105097062023-09-21 Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages Antignano, Ignazio Keane, Lily Capasso, Melania STAR Protoc Protocol Protein synthesis, or mRNA translation, is the biological process through which genetic information stored in messenger RNAs is encoded into proteins. Here, we present an optimized protocol for assessing the translation rate in mouse adult microglia and cultured bone-marrow-derived macrophages. We describe steps for isolating cells, treating them with a puromycin-analog probe, and fluorescently labeling the puromycylated-polypeptide chains. We then detail their quantification by flow cytometry or with a fluorescent plate reader. For complete details on the use and execution of this protocol, please refer to Keane et al. (2021).(1) Elsevier 2023-09-14 /pmc/articles/PMC10509706/ /pubmed/37713309 http://dx.doi.org/10.1016/j.xpro.2023.102559 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Antignano, Ignazio
Keane, Lily
Capasso, Melania
Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages
title Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages
title_full Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages
title_fullStr Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages
title_full_unstemmed Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages
title_short Assessing mRNA translation in mouse adult microglia and bone-marrow-derived macrophages
title_sort assessing mrna translation in mouse adult microglia and bone-marrow-derived macrophages
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509706/
https://www.ncbi.nlm.nih.gov/pubmed/37713309
http://dx.doi.org/10.1016/j.xpro.2023.102559
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