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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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) |
format | Online Article Text |
id | pubmed-10509706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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