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Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes

Mammalian cyclic dinucleotide 2′3′-cGAMP functions as a second messenger in innate immune response. Here, we report a protocol to utilize 2′3′-cGAMP photoaffinity probes to capture 2′3′-cGAMP-binding or 2′3′-cGAMP-interacting proteins from HeLa cell lysate for in-gel visualization by fluorescent ima...

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Detalles Bibliográficos
Autores principales: Hou, Yingjie, Lu, Heng, Sun, Le, Zhang, Yaoyang, Jiang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752945/
https://www.ncbi.nlm.nih.gov/pubmed/35036957
http://dx.doi.org/10.1016/j.xpro.2021.101076
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author Hou, Yingjie
Lu, Heng
Sun, Le
Zhang, Yaoyang
Jiang, Hong
author_facet Hou, Yingjie
Lu, Heng
Sun, Le
Zhang, Yaoyang
Jiang, Hong
author_sort Hou, Yingjie
collection PubMed
description Mammalian cyclic dinucleotide 2′3′-cGAMP functions as a second messenger in innate immune response. Here, we report a protocol to utilize 2′3′-cGAMP photoaffinity probes to capture 2′3′-cGAMP-binding or 2′3′-cGAMP-interacting proteins from HeLa cell lysate for in-gel visualization by fluorescent imaging or identification by SILAC–based quantitative MS. Further validation is also executed using photoaffinity probes to demonstrate the direct interaction of 2′3′-cGAMP with purified target proteins in vitro or endogenous target proteins in 293T cells. For complete details on the use and execution of this profile, please refer to Hou et al. (2021).
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spelling pubmed-87529452022-01-14 Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes Hou, Yingjie Lu, Heng Sun, Le Zhang, Yaoyang Jiang, Hong STAR Protoc Protocol Mammalian cyclic dinucleotide 2′3′-cGAMP functions as a second messenger in innate immune response. Here, we report a protocol to utilize 2′3′-cGAMP photoaffinity probes to capture 2′3′-cGAMP-binding or 2′3′-cGAMP-interacting proteins from HeLa cell lysate for in-gel visualization by fluorescent imaging or identification by SILAC–based quantitative MS. Further validation is also executed using photoaffinity probes to demonstrate the direct interaction of 2′3′-cGAMP with purified target proteins in vitro or endogenous target proteins in 293T cells. For complete details on the use and execution of this profile, please refer to Hou et al. (2021). Elsevier 2022-01-10 /pmc/articles/PMC8752945/ /pubmed/35036957 http://dx.doi.org/10.1016/j.xpro.2021.101076 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
Hou, Yingjie
Lu, Heng
Sun, Le
Zhang, Yaoyang
Jiang, Hong
Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes
title Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes
title_full Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes
title_fullStr Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes
title_full_unstemmed Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes
title_short Protocol for identification and validation of 2′3′-cGAMP-binding proteins by photoaffinity probes
title_sort protocol for identification and validation of 2′3′-cgamp-binding proteins by photoaffinity probes
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752945/
https://www.ncbi.nlm.nih.gov/pubmed/35036957
http://dx.doi.org/10.1016/j.xpro.2021.101076
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