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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...

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Detalles Bibliográficos
Autores principales: Furkert, David, Nadler-Holly, Michal, Fiedler, Dorothea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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).
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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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