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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...

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Detalles Bibliográficos
Autores principales: Cutts, Zachary William, Hong, Jessica M., Shao, Shirley, Tran, Alexander, Dimon, Michelle, Berndl, Marc, Wu, Diana, Pawlosky, Annalisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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).
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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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