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Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides
Systematic evolution of ligands by exponential enrichment (SELEX) encompasses a wide variety of high-throughput screening techniques for producing nucleic acid binders to molecular targets through directed evolution. We describe here the design and selection steps for discovery of DNA aptamers with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557731/ https://www.ncbi.nlm.nih.gov/pubmed/36208449 http://dx.doi.org/10.1016/j.xpro.2022.101724 |
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author | Cutts, Zachary William Hong, Jessica M. Shao, Shirley Tran, Alexander Dimon, Michelle Berndl, Marc Wu, Diana Pawlosky, Annalisa |
author_facet | Cutts, Zachary William Hong, Jessica M. Shao, Shirley Tran, Alexander Dimon, Michelle Berndl, Marc Wu, Diana Pawlosky, Annalisa |
author_sort | Cutts, Zachary William |
collection | PubMed |
description | Systematic evolution of ligands by exponential enrichment (SELEX) encompasses a wide variety of high-throughput screening techniques for producing nucleic acid binders to molecular targets through directed evolution. We describe here the design and selection steps for discovery of DNA aptamers with specificity for the two consecutive N-terminal amino acids (AAs) of a small peptide (8–10 amino acids). This bead-based method may be adapted for applications requiring binders which recognize a specific portion of the desired target. For complete details on the use and execution of this protocol, please refer to Hong et al. (2022). |
format | Online Article Text |
id | pubmed-9557731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95577312022-10-14 Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides Cutts, Zachary William Hong, Jessica M. Shao, Shirley Tran, Alexander Dimon, Michelle Berndl, Marc Wu, Diana Pawlosky, Annalisa STAR Protoc Protocol Systematic evolution of ligands by exponential enrichment (SELEX) encompasses a wide variety of high-throughput screening techniques for producing nucleic acid binders to molecular targets through directed evolution. We describe here the design and selection steps for discovery of DNA aptamers with specificity for the two consecutive N-terminal amino acids (AAs) of a small peptide (8–10 amino acids). This bead-based method may be adapted for applications requiring binders which recognize a specific portion of the desired target. For complete details on the use and execution of this protocol, please refer to Hong et al. (2022). Elsevier 2022-10-07 /pmc/articles/PMC9557731/ /pubmed/36208449 http://dx.doi.org/10.1016/j.xpro.2022.101724 Text en © 2022 The Authors 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 Cutts, Zachary William Hong, Jessica M. Shao, Shirley Tran, Alexander Dimon, Michelle Berndl, Marc Wu, Diana Pawlosky, Annalisa Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides |
title | Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides |
title_full | Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides |
title_fullStr | Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides |
title_full_unstemmed | Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides |
title_short | Target-switch SELEX: Screening with alternating targets to generate aptamers to conserved terminal dipeptides |
title_sort | target-switch selex: screening with alternating targets to generate aptamers to conserved terminal dipeptides |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557731/ https://www.ncbi.nlm.nih.gov/pubmed/36208449 http://dx.doi.org/10.1016/j.xpro.2022.101724 |
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