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Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes
This protocol describes an affinity enrichment approach from mammalian cell extracts to identify protein binding partners of inositol hexakisphosphate (InsP(6)) and 5-diphosphoinositol pentakisphosphate (5PP-InsP(5)), two important eukaryotic metabolites. The interactomes are annotated using mass sp...
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/PMC7811051/ https://www.ncbi.nlm.nih.gov/pubmed/33490990 http://dx.doi.org/10.1016/j.xpro.2020.100277 |
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author | Furkert, David Nadler-Holly, Michal Fiedler, Dorothea |
author_facet | Furkert, David Nadler-Holly, Michal Fiedler, Dorothea |
author_sort | Furkert, David |
collection | PubMed |
description | This protocol describes an affinity enrichment approach from mammalian cell extracts to identify protein binding partners of inositol hexakisphosphate (InsP(6)) and 5-diphosphoinositol pentakisphosphate (5PP-InsP(5)), two important eukaryotic metabolites. The interactomes are annotated using mass spectrometry-based proteomics, and comparison against a control resin can uncover hundreds of protein targets. Quantitative analysis of InsP(6)- versus 5PP-InsP(5)-binding proteins highlights specific protein-ligand interactions. The approach is applicable to different cells and organisms and will contribute to a mechanistic understanding of inositol poly- and pyrophosphate signaling. For complete details on the use and execution of this protocol, please refer to Furkert et al. (2020). |
format | Online Article Text |
id | pubmed-7811051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78110512021-01-22 Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes Furkert, David Nadler-Holly, Michal Fiedler, Dorothea STAR Protoc Protocol This protocol describes an affinity enrichment approach from mammalian cell extracts to identify protein binding partners of inositol hexakisphosphate (InsP(6)) and 5-diphosphoinositol pentakisphosphate (5PP-InsP(5)), two important eukaryotic metabolites. The interactomes are annotated using mass spectrometry-based proteomics, and comparison against a control resin can uncover hundreds of protein targets. Quantitative analysis of InsP(6)- versus 5PP-InsP(5)-binding proteins highlights specific protein-ligand interactions. The approach is applicable to different cells and organisms and will contribute to a mechanistic understanding of inositol poly- and pyrophosphate signaling. For complete details on the use and execution of this protocol, please refer to Furkert et al. (2020). Elsevier 2021-01-14 /pmc/articles/PMC7811051/ /pubmed/33490990 http://dx.doi.org/10.1016/j.xpro.2020.100277 Text en © 2020 The Authors http://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 Furkert, David Nadler-Holly, Michal Fiedler, Dorothea Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes |
title | Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes |
title_full | Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes |
title_fullStr | Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes |
title_full_unstemmed | Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes |
title_short | Affinity enrichment and identification of inositol poly- and pyrophosphate interactomes |
title_sort | affinity enrichment and identification of inositol poly- and pyrophosphate interactomes |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811051/ https://www.ncbi.nlm.nih.gov/pubmed/33490990 http://dx.doi.org/10.1016/j.xpro.2020.100277 |
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