Cargando…
Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells
The ascorbate peroxidase APEX2 is commonly used to study the neighborhood of a protein of interest by proximity-dependent biotinylation. Here, we describe a protocol for sample processing compatible with immunoblotting and mass spectrometry, suitable to specifically map the content of autophagosomes...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102175/ https://www.ncbi.nlm.nih.gov/pubmed/33997820 http://dx.doi.org/10.1016/j.xpro.2021.100506 |
_version_ | 1783689078639689728 |
---|---|
author | Zellner, Susanne Nalbach, Karsten Behrends, Christian |
author_facet | Zellner, Susanne Nalbach, Karsten Behrends, Christian |
author_sort | Zellner, Susanne |
collection | PubMed |
description | The ascorbate peroxidase APEX2 is commonly used to study the neighborhood of a protein of interest by proximity-dependent biotinylation. Here, we describe a protocol for sample processing compatible with immunoblotting and mass spectrometry, suitable to specifically map the content of autophagosomes and potentially other short-lived endomembrane transport vesicles without the need of subcellular fractionation. By combining live-cell biotinylation with proteinase K digestion of cell homogenates, proteins enriched in membrane-protected compartments can be readily enriched and identified. For complete details on the use and execution of this protocol, please refer to Zellner et al. (2021). |
format | Online Article Text |
id | pubmed-8102175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81021752021-05-14 Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells Zellner, Susanne Nalbach, Karsten Behrends, Christian STAR Protoc Protocol The ascorbate peroxidase APEX2 is commonly used to study the neighborhood of a protein of interest by proximity-dependent biotinylation. Here, we describe a protocol for sample processing compatible with immunoblotting and mass spectrometry, suitable to specifically map the content of autophagosomes and potentially other short-lived endomembrane transport vesicles without the need of subcellular fractionation. By combining live-cell biotinylation with proteinase K digestion of cell homogenates, proteins enriched in membrane-protected compartments can be readily enriched and identified. For complete details on the use and execution of this protocol, please refer to Zellner et al. (2021). Elsevier 2021-04-27 /pmc/articles/PMC8102175/ /pubmed/33997820 http://dx.doi.org/10.1016/j.xpro.2021.100506 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 Zellner, Susanne Nalbach, Karsten Behrends, Christian Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells |
title | Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells |
title_full | Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells |
title_fullStr | Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells |
title_full_unstemmed | Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells |
title_short | Autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells |
title_sort | autophagosome content profiling using proximity biotinylation proteomics coupled to protease digestion in mammalian cells |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102175/ https://www.ncbi.nlm.nih.gov/pubmed/33997820 http://dx.doi.org/10.1016/j.xpro.2021.100506 |
work_keys_str_mv | AT zellnersusanne autophagosomecontentprofilingusingproximitybiotinylationproteomicscoupledtoproteasedigestioninmammaliancells AT nalbachkarsten autophagosomecontentprofilingusingproximitybiotinylationproteomicscoupledtoproteasedigestioninmammaliancells AT behrendschristian autophagosomecontentprofilingusingproximitybiotinylationproteomicscoupledtoproteasedigestioninmammaliancells |