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High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro

High-throughput sequencing SELEX (HT-SELEX) is a powerful technique for unbiased determination of preferred target motifs of DNA-binding proteins in vitro. The procedure depends upon selection of DNA binding sites from a random library of oligonucleotides by purifying protein-DNA complexes and ampli...

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Detalles Bibliográficos
Autores principales: Pantier, Raphaël, Chhatbar, Kashyap, Alston, Grace, Lee, Heng Yang, Bird, Adrian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243297/
https://www.ncbi.nlm.nih.gov/pubmed/35776646
http://dx.doi.org/10.1016/j.xpro.2022.101490
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author Pantier, Raphaël
Chhatbar, Kashyap
Alston, Grace
Lee, Heng Yang
Bird, Adrian
author_facet Pantier, Raphaël
Chhatbar, Kashyap
Alston, Grace
Lee, Heng Yang
Bird, Adrian
author_sort Pantier, Raphaël
collection PubMed
description High-throughput sequencing SELEX (HT-SELEX) is a powerful technique for unbiased determination of preferred target motifs of DNA-binding proteins in vitro. The procedure depends upon selection of DNA binding sites from a random library of oligonucleotides by purifying protein-DNA complexes and amplifying bound DNA using the polymerase chain reaction. Here, we describe an optimized step-by-step protocol for HT-SELEX compatible with Illumina sequencing. We also introduce a bioinformatic pipeline (eme_selex) facilitating the detection of promiscuous DNA binding by analyzing the enrichment of all possible k-mers. For complete details on the use and execution of this protocol, please refer to Pantier et al. (2021).
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spelling pubmed-92432972022-07-01 High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro Pantier, Raphaël Chhatbar, Kashyap Alston, Grace Lee, Heng Yang Bird, Adrian STAR Protoc Protocol High-throughput sequencing SELEX (HT-SELEX) is a powerful technique for unbiased determination of preferred target motifs of DNA-binding proteins in vitro. The procedure depends upon selection of DNA binding sites from a random library of oligonucleotides by purifying protein-DNA complexes and amplifying bound DNA using the polymerase chain reaction. Here, we describe an optimized step-by-step protocol for HT-SELEX compatible with Illumina sequencing. We also introduce a bioinformatic pipeline (eme_selex) facilitating the detection of promiscuous DNA binding by analyzing the enrichment of all possible k-mers. For complete details on the use and execution of this protocol, please refer to Pantier et al. (2021). Elsevier 2022-06-23 /pmc/articles/PMC9243297/ /pubmed/35776646 http://dx.doi.org/10.1016/j.xpro.2022.101490 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
Pantier, Raphaël
Chhatbar, Kashyap
Alston, Grace
Lee, Heng Yang
Bird, Adrian
High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro
title High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro
title_full High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro
title_fullStr High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro
title_full_unstemmed High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro
title_short High-throughput sequencing SELEX for the determination of DNA-binding protein specificities in vitro
title_sort high-throughput sequencing selex for the determination of dna-binding protein specificities in vitro
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9243297/
https://www.ncbi.nlm.nih.gov/pubmed/35776646
http://dx.doi.org/10.1016/j.xpro.2022.101490
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