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Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay

Transcription factors (TFs) play a pivotal role in gene expression, and their DNA binding is the prerequisite to instigating gene transcription. Here, we present a protocol that exploits the proximity ligation assay technique to measure the DNA-binding activities of TFs in situ at the single-cell re...

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Autores principales: Ram, Babul Moni, Dai, Chengkai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651771/
https://www.ncbi.nlm.nih.gov/pubmed/37917578
http://dx.doi.org/10.1016/j.xpro.2023.102692
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author Ram, Babul Moni
Dai, Chengkai
author_facet Ram, Babul Moni
Dai, Chengkai
author_sort Ram, Babul Moni
collection PubMed
description Transcription factors (TFs) play a pivotal role in gene expression, and their DNA binding is the prerequisite to instigating gene transcription. Here, we present a protocol that exploits the proximity ligation assay technique to measure the DNA-binding activities of TFs in situ at the single-cell resolution. We describe steps for immunostaining with specific antibodies against double-stranded DNA and the TFs of interest, probe incubation, proximity ligation, and signal amplification. We then detail procedures for imaging and image analysis. For complete details on the use and execution of this protocol, please refer to Dai et al. (2015)(1) and Xu et al. (2023).(2)
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spelling pubmed-106517712023-11-02 Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay Ram, Babul Moni Dai, Chengkai STAR Protoc Protocol Transcription factors (TFs) play a pivotal role in gene expression, and their DNA binding is the prerequisite to instigating gene transcription. Here, we present a protocol that exploits the proximity ligation assay technique to measure the DNA-binding activities of TFs in situ at the single-cell resolution. We describe steps for immunostaining with specific antibodies against double-stranded DNA and the TFs of interest, probe incubation, proximity ligation, and signal amplification. We then detail procedures for imaging and image analysis. For complete details on the use and execution of this protocol, please refer to Dai et al. (2015)(1) and Xu et al. (2023).(2) Elsevier 2023-11-02 /pmc/articles/PMC10651771/ /pubmed/37917578 http://dx.doi.org/10.1016/j.xpro.2023.102692 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Ram, Babul Moni
Dai, Chengkai
Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay
title Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay
title_full Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay
title_fullStr Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay
title_full_unstemmed Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay
title_short Detection of the DNA binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay
title_sort detection of the dna binding of transcription factors in situ at the single-cell resolution in cultured cells by proximity ligation assay
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651771/
https://www.ncbi.nlm.nih.gov/pubmed/37917578
http://dx.doi.org/10.1016/j.xpro.2023.102692
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AT daichengkai detectionofthednabindingoftranscriptionfactorsinsituatthesinglecellresolutioninculturedcellsbyproximityligationassay