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Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing

The identification of nucleic acid aptamers would be advanced if they could be obtained after fewer rounds of selection and amplification. In this paper the identification of bivalent aptamers for thrombin by SELEX and single-step selection are compared using next generation sequencing and motif fin...

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Detalles Bibliográficos
Autores principales: Wilson, Robert, Bourne, Christian, Chaudhuri, Roy R., Gregory, Richard, Kenny, John, Cossins, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070925/
https://www.ncbi.nlm.nih.gov/pubmed/24963654
http://dx.doi.org/10.1371/journal.pone.0100572
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author Wilson, Robert
Bourne, Christian
Chaudhuri, Roy R.
Gregory, Richard
Kenny, John
Cossins, Andrew
author_facet Wilson, Robert
Bourne, Christian
Chaudhuri, Roy R.
Gregory, Richard
Kenny, John
Cossins, Andrew
author_sort Wilson, Robert
collection PubMed
description The identification of nucleic acid aptamers would be advanced if they could be obtained after fewer rounds of selection and amplification. In this paper the identification of bivalent aptamers for thrombin by SELEX and single-step selection are compared using next generation sequencing and motif finding informatics. Results show that similar aptamers are identified by both methods. This is significant because it shows that next generation sequencing and motif finding informatics have the potential to simplify the selection of aptamers by avoiding multiple rounds of enzymatic transcription and amplification.
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spelling pubmed-40709252014-06-27 Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing Wilson, Robert Bourne, Christian Chaudhuri, Roy R. Gregory, Richard Kenny, John Cossins, Andrew PLoS One Research Article The identification of nucleic acid aptamers would be advanced if they could be obtained after fewer rounds of selection and amplification. In this paper the identification of bivalent aptamers for thrombin by SELEX and single-step selection are compared using next generation sequencing and motif finding informatics. Results show that similar aptamers are identified by both methods. This is significant because it shows that next generation sequencing and motif finding informatics have the potential to simplify the selection of aptamers by avoiding multiple rounds of enzymatic transcription and amplification. Public Library of Science 2014-06-25 /pmc/articles/PMC4070925/ /pubmed/24963654 http://dx.doi.org/10.1371/journal.pone.0100572 Text en © 2014 Wilson et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wilson, Robert
Bourne, Christian
Chaudhuri, Roy R.
Gregory, Richard
Kenny, John
Cossins, Andrew
Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing
title Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing
title_full Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing
title_fullStr Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing
title_full_unstemmed Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing
title_short Single-Step Selection of Bivalent Aptamers Validated by Comparison with SELEX Using High-Throughput Sequencing
title_sort single-step selection of bivalent aptamers validated by comparison with selex using high-throughput sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070925/
https://www.ncbi.nlm.nih.gov/pubmed/24963654
http://dx.doi.org/10.1371/journal.pone.0100572
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