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Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS

In contrast to sophisticated high-throughput sequencing tools for genomic DNA, analytical tools for comparing secondary structure features between multiple single-stranded DNA sequences are less developed. For single-stranded nucleic acid ligands called aptamers, secondary structure is widely though...

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Detalles Bibliográficos
Autores principales: Sullivan, Richard, Adams, Mary Catherine, Naik, Rajesh R., Milam, Valeria T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515186/
https://www.ncbi.nlm.nih.gov/pubmed/31010064
http://dx.doi.org/10.3390/molecules24081572
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author Sullivan, Richard
Adams, Mary Catherine
Naik, Rajesh R.
Milam, Valeria T.
author_facet Sullivan, Richard
Adams, Mary Catherine
Naik, Rajesh R.
Milam, Valeria T.
author_sort Sullivan, Richard
collection PubMed
description In contrast to sophisticated high-throughput sequencing tools for genomic DNA, analytical tools for comparing secondary structure features between multiple single-stranded DNA sequences are less developed. For single-stranded nucleic acid ligands called aptamers, secondary structure is widely thought to play a pivotal role in driving recognition-based binding activity between an aptamer sequence and its specific target. Here, we employ a competition-based aptamer screening platform called CompELS to identify DNA aptamers for a colloidal target. We then analyze predicted secondary structures of the aptamers and a large population of random sequences to identify sequence features and patterns. Our secondary structure analysis identifies patterns ranging from position-dependent score matrixes of individual structural elements to position-independent consensus domains resulting from global alignment.
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spelling pubmed-65151862019-05-30 Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS Sullivan, Richard Adams, Mary Catherine Naik, Rajesh R. Milam, Valeria T. Molecules Article In contrast to sophisticated high-throughput sequencing tools for genomic DNA, analytical tools for comparing secondary structure features between multiple single-stranded DNA sequences are less developed. For single-stranded nucleic acid ligands called aptamers, secondary structure is widely thought to play a pivotal role in driving recognition-based binding activity between an aptamer sequence and its specific target. Here, we employ a competition-based aptamer screening platform called CompELS to identify DNA aptamers for a colloidal target. We then analyze predicted secondary structures of the aptamers and a large population of random sequences to identify sequence features and patterns. Our secondary structure analysis identifies patterns ranging from position-dependent score matrixes of individual structural elements to position-independent consensus domains resulting from global alignment. MDPI 2019-04-21 /pmc/articles/PMC6515186/ /pubmed/31010064 http://dx.doi.org/10.3390/molecules24081572 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sullivan, Richard
Adams, Mary Catherine
Naik, Rajesh R.
Milam, Valeria T.
Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS
title Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS
title_full Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS
title_fullStr Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS
title_full_unstemmed Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS
title_short Analyzing Secondary Structure Patterns in DNA Aptamers Identified via CompELS
title_sort analyzing secondary structure patterns in dna aptamers identified via compels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515186/
https://www.ncbi.nlm.nih.gov/pubmed/31010064
http://dx.doi.org/10.3390/molecules24081572
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