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TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells

TOP1 CAD-seq enables mapping of TOP1 sites of covalent engagement with DNA. The procedure depends upon enrichment of DNA-covalent adducts using chaotropic salts and immunoprecipitation with an antibody specific for TOP1. Here, we describe a step-by-step protocol compatible with Illumina sequencing a...

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Autores principales: Kuzin, Vladislav, Wiegard, Anika, Cameron, Donald P., Baranello, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356208/
https://www.ncbi.nlm.nih.gov/pubmed/35942340
http://dx.doi.org/10.1016/j.xpro.2022.101581
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author Kuzin, Vladislav
Wiegard, Anika
Cameron, Donald P.
Baranello, Laura
author_facet Kuzin, Vladislav
Wiegard, Anika
Cameron, Donald P.
Baranello, Laura
author_sort Kuzin, Vladislav
collection PubMed
description TOP1 CAD-seq enables mapping of TOP1 sites of covalent engagement with DNA. The procedure depends upon enrichment of DNA-covalent adducts using chaotropic salts and immunoprecipitation with an antibody specific for TOP1. Here, we describe a step-by-step protocol compatible with Illumina sequencing and bioinformatic pipeline for preliminary data analysis. Compared to other approaches for the genomic study of topoisomerases, TOP1 CAD-seq provides information about active TOP1 engaged on the DNA, taking advantage of low background due to absence of crosslinking. For complete details on the use and execution of this protocol, please refer to Das et al. (2022).
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spelling pubmed-93562082022-08-07 TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells Kuzin, Vladislav Wiegard, Anika Cameron, Donald P. Baranello, Laura STAR Protoc Protocol TOP1 CAD-seq enables mapping of TOP1 sites of covalent engagement with DNA. The procedure depends upon enrichment of DNA-covalent adducts using chaotropic salts and immunoprecipitation with an antibody specific for TOP1. Here, we describe a step-by-step protocol compatible with Illumina sequencing and bioinformatic pipeline for preliminary data analysis. Compared to other approaches for the genomic study of topoisomerases, TOP1 CAD-seq provides information about active TOP1 engaged on the DNA, taking advantage of low background due to absence of crosslinking. For complete details on the use and execution of this protocol, please refer to Das et al. (2022). Elsevier 2022-08-01 /pmc/articles/PMC9356208/ /pubmed/35942340 http://dx.doi.org/10.1016/j.xpro.2022.101581 Text en © 2022 The Author(s) 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
Kuzin, Vladislav
Wiegard, Anika
Cameron, Donald P.
Baranello, Laura
TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells
title TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells
title_full TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells
title_fullStr TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells
title_full_unstemmed TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells
title_short TOP1 CAD-seq: A protocol to map catalytically engaged topoisomerase 1 in human cells
title_sort top1 cad-seq: a protocol to map catalytically engaged topoisomerase 1 in human cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356208/
https://www.ncbi.nlm.nih.gov/pubmed/35942340
http://dx.doi.org/10.1016/j.xpro.2022.101581
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