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Chromatin-Bound Proteome Profiling by Genome Capture

De novo identification of chromatin interactors can reveal unexpected pathways relevant to physiology and human disease. Inspired by the DNA mediated chromatin pull-down (Dm-ChP) technology (also known as iPOND [isolation of proteins on nascent DNA]) for the proteomic characterization of nascent DNA...

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Detalles Bibliográficos
Autores principales: Aranda, Sergi, Borràs, Eva, Sabidó, Eduard, Di Croce, Luciano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580076/
https://www.ncbi.nlm.nih.gov/pubmed/33111072
http://dx.doi.org/10.1016/j.xpro.2020.100014
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author Aranda, Sergi
Borràs, Eva
Sabidó, Eduard
Di Croce, Luciano
author_facet Aranda, Sergi
Borràs, Eva
Sabidó, Eduard
Di Croce, Luciano
author_sort Aranda, Sergi
collection PubMed
description De novo identification of chromatin interactors can reveal unexpected pathways relevant to physiology and human disease. Inspired by the DNA mediated chromatin pull-down (Dm-ChP) technology (also known as iPOND [isolation of proteins on nascent DNA]) for the proteomic characterization of nascent DNA, we have recently reported a new experimental protocol that allows for the identification of proteins on total DNA (iPOTD) for bulk chromatome profiling and de novo identification of chromatin-bound proteins. Here, we detail a step-by-step protocol to survey the cellular chromatin-bound proteome in a simple, robust, and unbiased manner. For complete details on the use and execution of this protocol, please refer to Aranda et al. (2019).
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spelling pubmed-75800762020-10-26 Chromatin-Bound Proteome Profiling by Genome Capture Aranda, Sergi Borràs, Eva Sabidó, Eduard Di Croce, Luciano STAR Protoc Protocol De novo identification of chromatin interactors can reveal unexpected pathways relevant to physiology and human disease. Inspired by the DNA mediated chromatin pull-down (Dm-ChP) technology (also known as iPOND [isolation of proteins on nascent DNA]) for the proteomic characterization of nascent DNA, we have recently reported a new experimental protocol that allows for the identification of proteins on total DNA (iPOTD) for bulk chromatome profiling and de novo identification of chromatin-bound proteins. Here, we detail a step-by-step protocol to survey the cellular chromatin-bound proteome in a simple, robust, and unbiased manner. For complete details on the use and execution of this protocol, please refer to Aranda et al. (2019). Elsevier 2020-06-03 /pmc/articles/PMC7580076/ /pubmed/33111072 http://dx.doi.org/10.1016/j.xpro.2020.100014 Text en © 2020. 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
Aranda, Sergi
Borràs, Eva
Sabidó, Eduard
Di Croce, Luciano
Chromatin-Bound Proteome Profiling by Genome Capture
title Chromatin-Bound Proteome Profiling by Genome Capture
title_full Chromatin-Bound Proteome Profiling by Genome Capture
title_fullStr Chromatin-Bound Proteome Profiling by Genome Capture
title_full_unstemmed Chromatin-Bound Proteome Profiling by Genome Capture
title_short Chromatin-Bound Proteome Profiling by Genome Capture
title_sort chromatin-bound proteome profiling by genome capture
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580076/
https://www.ncbi.nlm.nih.gov/pubmed/33111072
http://dx.doi.org/10.1016/j.xpro.2020.100014
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