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Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing

The development of novel affinity probes for cancer biomarkers may enable powerful improvements in analytical methods for detecting and treating cancer. In this report, we describe our use of capillary electrophoresis (CE) as the separation mechanism in the process of selecting DNA aptamers with aff...

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Autores principales: Eaton, Rachel M., Shallcross, Jamie A., Mael, Liora E., Mears, Kepler S., Minkoff, Lisa, Scoville, Delia J., Whelan, Rebecca J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551533/
https://www.ncbi.nlm.nih.gov/pubmed/25863801
http://dx.doi.org/10.1007/s00216-015-8665-7
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author Eaton, Rachel M.
Shallcross, Jamie A.
Mael, Liora E.
Mears, Kepler S.
Minkoff, Lisa
Scoville, Delia J.
Whelan, Rebecca J.
author_facet Eaton, Rachel M.
Shallcross, Jamie A.
Mael, Liora E.
Mears, Kepler S.
Minkoff, Lisa
Scoville, Delia J.
Whelan, Rebecca J.
author_sort Eaton, Rachel M.
collection PubMed
description The development of novel affinity probes for cancer biomarkers may enable powerful improvements in analytical methods for detecting and treating cancer. In this report, we describe our use of capillary electrophoresis (CE) as the separation mechanism in the process of selecting DNA aptamers with affinity for the ovarian cancer biomarker HE4. Rather than the conventional use of cloning and sequencing as the last step in the aptamer selection process, we used high-throughput sequencing on an Illumina platform. This data-rich approach, combined with a bioinformatics pipeline based on freely available computational tools, enabled the entirety of the selection process—and not only its endpoint—to be characterized. Affinity probe CE and fluorescence anisotropy assays demonstrate the binding affinity of a set of aptamer candidates identified through this bioinformatics approach. [Figure: see text]
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spelling pubmed-45515332015-09-01 Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing Eaton, Rachel M. Shallcross, Jamie A. Mael, Liora E. Mears, Kepler S. Minkoff, Lisa Scoville, Delia J. Whelan, Rebecca J. Anal Bioanal Chem Research Paper The development of novel affinity probes for cancer biomarkers may enable powerful improvements in analytical methods for detecting and treating cancer. In this report, we describe our use of capillary electrophoresis (CE) as the separation mechanism in the process of selecting DNA aptamers with affinity for the ovarian cancer biomarker HE4. Rather than the conventional use of cloning and sequencing as the last step in the aptamer selection process, we used high-throughput sequencing on an Illumina platform. This data-rich approach, combined with a bioinformatics pipeline based on freely available computational tools, enabled the entirety of the selection process—and not only its endpoint—to be characterized. Affinity probe CE and fluorescence anisotropy assays demonstrate the binding affinity of a set of aptamer candidates identified through this bioinformatics approach. [Figure: see text] Springer Berlin Heidelberg 2015-04-12 2015 /pmc/articles/PMC4551533/ /pubmed/25863801 http://dx.doi.org/10.1007/s00216-015-8665-7 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Paper
Eaton, Rachel M.
Shallcross, Jamie A.
Mael, Liora E.
Mears, Kepler S.
Minkoff, Lisa
Scoville, Delia J.
Whelan, Rebecca J.
Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing
title Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing
title_full Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing
title_fullStr Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing
title_full_unstemmed Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing
title_short Selection of DNA aptamers for ovarian cancer biomarker HE4 using CE-SELEX and high-throughput sequencing
title_sort selection of dna aptamers for ovarian cancer biomarker he4 using ce-selex and high-throughput sequencing
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551533/
https://www.ncbi.nlm.nih.gov/pubmed/25863801
http://dx.doi.org/10.1007/s00216-015-8665-7
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