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A proximity labeling protocol to probe proximity interactions in C. elegans

Enzyme-catalyzed proximity labeling (PL) has emerged as a critical approach for identifying protein-protein proximity interactions in cells; however, PL techniques were not historically practical in living multicellular organisms due to technical limitations. Here, we present a protocol for applying...

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Detalles Bibliográficos
Autores principales: Sanchez, Ariana D., Feldman, Jessica L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649953/
https://www.ncbi.nlm.nih.gov/pubmed/34927095
http://dx.doi.org/10.1016/j.xpro.2021.100986
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author Sanchez, Ariana D.
Feldman, Jessica L.
author_facet Sanchez, Ariana D.
Feldman, Jessica L.
author_sort Sanchez, Ariana D.
collection PubMed
description Enzyme-catalyzed proximity labeling (PL) has emerged as a critical approach for identifying protein-protein proximity interactions in cells; however, PL techniques were not historically practical in living multicellular organisms due to technical limitations. Here, we present a protocol for applying PL to living C. elegans using the biotin ligase mutant enzyme TurboID. We demonstrated PL in a tissue-specific and region-specific manner by focusing on non-centrosomal MTOCs (ncMTOCs) of intestinal cells. This protocol is useful for targeted in vivo protein network profiling. For complete details on the use and execution of this protocol, please refer to Sanchez et al. (2021).
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spelling pubmed-86499532021-12-17 A proximity labeling protocol to probe proximity interactions in C. elegans Sanchez, Ariana D. Feldman, Jessica L. STAR Protoc Protocol Enzyme-catalyzed proximity labeling (PL) has emerged as a critical approach for identifying protein-protein proximity interactions in cells; however, PL techniques were not historically practical in living multicellular organisms due to technical limitations. Here, we present a protocol for applying PL to living C. elegans using the biotin ligase mutant enzyme TurboID. We demonstrated PL in a tissue-specific and region-specific manner by focusing on non-centrosomal MTOCs (ncMTOCs) of intestinal cells. This protocol is useful for targeted in vivo protein network profiling. For complete details on the use and execution of this protocol, please refer to Sanchez et al. (2021). Elsevier 2021-12-02 /pmc/articles/PMC8649953/ /pubmed/34927095 http://dx.doi.org/10.1016/j.xpro.2021.100986 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
Sanchez, Ariana D.
Feldman, Jessica L.
A proximity labeling protocol to probe proximity interactions in C. elegans
title A proximity labeling protocol to probe proximity interactions in C. elegans
title_full A proximity labeling protocol to probe proximity interactions in C. elegans
title_fullStr A proximity labeling protocol to probe proximity interactions in C. elegans
title_full_unstemmed A proximity labeling protocol to probe proximity interactions in C. elegans
title_short A proximity labeling protocol to probe proximity interactions in C. elegans
title_sort proximity labeling protocol to probe proximity interactions in c. elegans
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649953/
https://www.ncbi.nlm.nih.gov/pubmed/34927095
http://dx.doi.org/10.1016/j.xpro.2021.100986
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