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Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice
Secreted polypeptides represent a fundamental axis of intercellular communication. Here, we present a protocol for the cell type-specific biotinylation, enrichment, and proteomic profiling of secreted plasma proteins directly in mice. This protocol uses conditional “turn-on” adeno-associated viruses...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672099/ https://www.ncbi.nlm.nih.gov/pubmed/34950890 http://dx.doi.org/10.1016/j.xpro.2021.101014 |
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author | Wei, Wei Riley, Nicholas M. Lyu, Xuchao Bertozzi, Carolyn R. Long, Jonathan Z. |
author_facet | Wei, Wei Riley, Nicholas M. Lyu, Xuchao Bertozzi, Carolyn R. Long, Jonathan Z. |
author_sort | Wei, Wei |
collection | PubMed |
description | Secreted polypeptides represent a fundamental axis of intercellular communication. Here, we present a protocol for the cell type-specific biotinylation, enrichment, and proteomic profiling of secreted plasma proteins directly in mice. This protocol uses conditional “turn-on” adeno-associated viruses expressing an endoplasmic reticulum-targeted biotin ligase to globally biotinylate proteins of the secretory pathway in a cell type-specific manner. Biotinylated secreted proteins can be directly purified from blood plasma and analyzed by SDS-PAGE gel or shotgun proteomics. For complete information on the generation and use of this protocol, please refer to Wei et al. (2021). |
format | Online Article Text |
id | pubmed-8672099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86720992021-12-22 Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice Wei, Wei Riley, Nicholas M. Lyu, Xuchao Bertozzi, Carolyn R. Long, Jonathan Z. STAR Protoc Protocol Secreted polypeptides represent a fundamental axis of intercellular communication. Here, we present a protocol for the cell type-specific biotinylation, enrichment, and proteomic profiling of secreted plasma proteins directly in mice. This protocol uses conditional “turn-on” adeno-associated viruses expressing an endoplasmic reticulum-targeted biotin ligase to globally biotinylate proteins of the secretory pathway in a cell type-specific manner. Biotinylated secreted proteins can be directly purified from blood plasma and analyzed by SDS-PAGE gel or shotgun proteomics. For complete information on the generation and use of this protocol, please refer to Wei et al. (2021). Elsevier 2021-12-11 /pmc/articles/PMC8672099/ /pubmed/34950890 http://dx.doi.org/10.1016/j.xpro.2021.101014 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 Wei, Wei Riley, Nicholas M. Lyu, Xuchao Bertozzi, Carolyn R. Long, Jonathan Z. Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice |
title | Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice |
title_full | Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice |
title_fullStr | Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice |
title_full_unstemmed | Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice |
title_short | Protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice |
title_sort | protocol for cell type-specific labeling, enrichment, and proteomic profiling of plasma proteins in mice |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672099/ https://www.ncbi.nlm.nih.gov/pubmed/34950890 http://dx.doi.org/10.1016/j.xpro.2021.101014 |
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