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Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement

Co-immunoprecipitation or pull-down assays are frequently used to analyze protein–protein interactions. In these experiments, western blotting is commonly used to detect prey proteins. However, sensitivity and quantification problems remain in this detection system. Recently, the HiBiT-tag-dependent...

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Detalles Bibliográficos
Autores principales: Arakawa, Masashi, Morita, Eiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bio-Protocol 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031519/
https://www.ncbi.nlm.nih.gov/pubmed/36968438
http://dx.doi.org/10.21769/BioProtoc.4640
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author Arakawa, Masashi
Morita, Eiji
author_facet Arakawa, Masashi
Morita, Eiji
author_sort Arakawa, Masashi
collection PubMed
description Co-immunoprecipitation or pull-down assays are frequently used to analyze protein–protein interactions. In these experiments, western blotting is commonly used to detect prey proteins. However, sensitivity and quantification problems remain in this detection system. Recently, the HiBiT-tag-dependent NanoLuc luciferase system was developed as a highly sensitive detection system for small amounts of proteins. In this report, we introduce the method of using HiBiT technology for the detection of prey protein in a pull-down assay. Using this protocol, we demonstrate the formation of a ternary complex consisting of Japanese encephalitis virus NS4B and two host factors, namely valosin-containing protein, and nuclear protein localization protein 4, which is a critical biological event during flavivirus replication in cells.
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spelling pubmed-100315192023-03-23 Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement Arakawa, Masashi Morita, Eiji Bio Protoc Methods Article Co-immunoprecipitation or pull-down assays are frequently used to analyze protein–protein interactions. In these experiments, western blotting is commonly used to detect prey proteins. However, sensitivity and quantification problems remain in this detection system. Recently, the HiBiT-tag-dependent NanoLuc luciferase system was developed as a highly sensitive detection system for small amounts of proteins. In this report, we introduce the method of using HiBiT technology for the detection of prey protein in a pull-down assay. Using this protocol, we demonstrate the formation of a ternary complex consisting of Japanese encephalitis virus NS4B and two host factors, namely valosin-containing protein, and nuclear protein localization protein 4, which is a critical biological event during flavivirus replication in cells. Bio-Protocol 2023-03-20 /pmc/articles/PMC10031519/ /pubmed/36968438 http://dx.doi.org/10.21769/BioProtoc.4640 Text en Copyright © 2023 The Authors; exclusive licensee Bio-protocol LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Methods Article
Arakawa, Masashi
Morita, Eiji
Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement
title Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement
title_full Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement
title_fullStr Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement
title_full_unstemmed Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement
title_short Protein Pull-down Assay Using HiBiT-tag-dependent Luciferase Activity Measurement
title_sort protein pull-down assay using hibit-tag-dependent luciferase activity measurement
topic Methods Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031519/
https://www.ncbi.nlm.nih.gov/pubmed/36968438
http://dx.doi.org/10.21769/BioProtoc.4640
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