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Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans

We present an optimized protocol for in vivo affinity purification proteomics and biochemistry using the model organism C. elegans. We describe steps for target tagging, large-scale culture, affinity purification using a cryomill, mass spectrometry and validation of candidate binding proteins. Our a...

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Detalles Bibliográficos
Autores principales: Desbois, Muriel, Pak, Joseph S., Opperman, Karla J., Giles, Andrew C., Grill, Brock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323129/
https://www.ncbi.nlm.nih.gov/pubmed/37294631
http://dx.doi.org/10.1016/j.xpro.2023.102262
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author Desbois, Muriel
Pak, Joseph S.
Opperman, Karla J.
Giles, Andrew C.
Grill, Brock
author_facet Desbois, Muriel
Pak, Joseph S.
Opperman, Karla J.
Giles, Andrew C.
Grill, Brock
author_sort Desbois, Muriel
collection PubMed
description We present an optimized protocol for in vivo affinity purification proteomics and biochemistry using the model organism C. elegans. We describe steps for target tagging, large-scale culture, affinity purification using a cryomill, mass spectrometry and validation of candidate binding proteins. Our approach has proven successful for identifying protein-protein interactions and signaling networks with verified functional relevance. Our protocol is also suitable for biochemical evaluation of protein-protein interactions in vivo. For complete details on the use and execution of this protocol, please refer to Crawley et al.,(1) Giles et al.,(2) and Desbois et al.(3)
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spelling pubmed-103231292023-07-07 Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans Desbois, Muriel Pak, Joseph S. Opperman, Karla J. Giles, Andrew C. Grill, Brock STAR Protoc Protocol We present an optimized protocol for in vivo affinity purification proteomics and biochemistry using the model organism C. elegans. We describe steps for target tagging, large-scale culture, affinity purification using a cryomill, mass spectrometry and validation of candidate binding proteins. Our approach has proven successful for identifying protein-protein interactions and signaling networks with verified functional relevance. Our protocol is also suitable for biochemical evaluation of protein-protein interactions in vivo. For complete details on the use and execution of this protocol, please refer to Crawley et al.,(1) Giles et al.,(2) and Desbois et al.(3) Elsevier 2023-06-08 /pmc/articles/PMC10323129/ /pubmed/37294631 http://dx.doi.org/10.1016/j.xpro.2023.102262 Text en © 2023 The Authors 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
Desbois, Muriel
Pak, Joseph S.
Opperman, Karla J.
Giles, Andrew C.
Grill, Brock
Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans
title Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans
title_full Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans
title_fullStr Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans
title_full_unstemmed Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans
title_short Optimized protocol for in vivo affinity purification proteomics and biochemistry using C. elegans
title_sort optimized protocol for in vivo affinity purification proteomics and biochemistry using c. elegans
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323129/
https://www.ncbi.nlm.nih.gov/pubmed/37294631
http://dx.doi.org/10.1016/j.xpro.2023.102262
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