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Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes

Selective identification of newly synthesized proteins is challenging because all proteins, both existing and nascent, have the same amino acid pool and are therefore chemically indistinguishable. L-homopropargylglycine is an amino acid analog of methionine containing an alkyne moiety that can under...

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Detalles Bibliográficos
Autores principales: Shen, Yuqian, Liu, Wenhua, Zuo, Jian, Han, Junhai, Zhang, Zi Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220402/
https://www.ncbi.nlm.nih.gov/pubmed/34189479
http://dx.doi.org/10.1016/j.xpro.2021.100616
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author Shen, Yuqian
Liu, Wenhua
Zuo, Jian
Han, Junhai
Zhang, Zi Chao
author_facet Shen, Yuqian
Liu, Wenhua
Zuo, Jian
Han, Junhai
Zhang, Zi Chao
author_sort Shen, Yuqian
collection PubMed
description Selective identification of newly synthesized proteins is challenging because all proteins, both existing and nascent, have the same amino acid pool and are therefore chemically indistinguishable. L-homopropargylglycine is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor. Here, we present an integrated tool based on immunofluorescence staining to accurately trace and localize the newly synthesized protein in isolated primary mouse hepatocytes. For complete details on the use and execution of this protocol, please refer to Shen et al. (2021).
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spelling pubmed-82204022021-06-28 Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes Shen, Yuqian Liu, Wenhua Zuo, Jian Han, Junhai Zhang, Zi Chao STAR Protoc Protocol Selective identification of newly synthesized proteins is challenging because all proteins, both existing and nascent, have the same amino acid pool and are therefore chemically indistinguishable. L-homopropargylglycine is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor. Here, we present an integrated tool based on immunofluorescence staining to accurately trace and localize the newly synthesized protein in isolated primary mouse hepatocytes. For complete details on the use and execution of this protocol, please refer to Shen et al. (2021). Elsevier 2021-06-17 /pmc/articles/PMC8220402/ /pubmed/34189479 http://dx.doi.org/10.1016/j.xpro.2021.100616 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Shen, Yuqian
Liu, Wenhua
Zuo, Jian
Han, Junhai
Zhang, Zi Chao
Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes
title Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes
title_full Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes
title_fullStr Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes
title_full_unstemmed Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes
title_short Protocol for visualizing newly synthesized proteins in primary mouse hepatocytes
title_sort protocol for visualizing newly synthesized proteins in primary mouse hepatocytes
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220402/
https://www.ncbi.nlm.nih.gov/pubmed/34189479
http://dx.doi.org/10.1016/j.xpro.2021.100616
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