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A smart polymer for sequence-selective binding, pulldown, and release of DNA targets

Selective isolation of DNA is crucial for applications in biology, bionanotechnology, clinical diagnostics and forensics. We herein report a smart methanol-responsive polymer (MeRPy) that can be programmed to bind and separate single- as well as double-stranded DNA targets. Captured targets are quic...

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Autores principales: Krieg, Elisha, Gupta, Krishna, Dahl, Andreas, Lesche, Mathias, Boye, Susanne, Lederer, Albena, Shih, William M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351716/
https://www.ncbi.nlm.nih.gov/pubmed/32651444
http://dx.doi.org/10.1038/s42003-020-1082-2
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author Krieg, Elisha
Gupta, Krishna
Dahl, Andreas
Lesche, Mathias
Boye, Susanne
Lederer, Albena
Shih, William M.
author_facet Krieg, Elisha
Gupta, Krishna
Dahl, Andreas
Lesche, Mathias
Boye, Susanne
Lederer, Albena
Shih, William M.
author_sort Krieg, Elisha
collection PubMed
description Selective isolation of DNA is crucial for applications in biology, bionanotechnology, clinical diagnostics and forensics. We herein report a smart methanol-responsive polymer (MeRPy) that can be programmed to bind and separate single- as well as double-stranded DNA targets. Captured targets are quickly isolated and released back into solution by denaturation (sequence-agnostic) or toehold-mediated strand displacement (sequence-selective). The latter mode allows 99.8% efficient removal of unwanted sequences and 79% recovery of highly pure target sequences. We applied MeRPy for the depletion of insulin, glucagon, and transthyretin cDNA from clinical next-generation sequencing (NGS) libraries. This step improved the data quality for low-abundance transcripts in expression profiles of pancreatic tissues. Its low cost, scalability, high stability and ease of use make MeRPy suitable for diverse applications in research and clinical laboratories, including enhancement of NGS libraries, extraction of DNA from biological samples, preparative-scale DNA isolations, and sorting of DNA-labeled non-nucleic acid targets.
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spelling pubmed-73517162020-07-13 A smart polymer for sequence-selective binding, pulldown, and release of DNA targets Krieg, Elisha Gupta, Krishna Dahl, Andreas Lesche, Mathias Boye, Susanne Lederer, Albena Shih, William M. Commun Biol Article Selective isolation of DNA is crucial for applications in biology, bionanotechnology, clinical diagnostics and forensics. We herein report a smart methanol-responsive polymer (MeRPy) that can be programmed to bind and separate single- as well as double-stranded DNA targets. Captured targets are quickly isolated and released back into solution by denaturation (sequence-agnostic) or toehold-mediated strand displacement (sequence-selective). The latter mode allows 99.8% efficient removal of unwanted sequences and 79% recovery of highly pure target sequences. We applied MeRPy for the depletion of insulin, glucagon, and transthyretin cDNA from clinical next-generation sequencing (NGS) libraries. This step improved the data quality for low-abundance transcripts in expression profiles of pancreatic tissues. Its low cost, scalability, high stability and ease of use make MeRPy suitable for diverse applications in research and clinical laboratories, including enhancement of NGS libraries, extraction of DNA from biological samples, preparative-scale DNA isolations, and sorting of DNA-labeled non-nucleic acid targets. Nature Publishing Group UK 2020-07-10 /pmc/articles/PMC7351716/ /pubmed/32651444 http://dx.doi.org/10.1038/s42003-020-1082-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Krieg, Elisha
Gupta, Krishna
Dahl, Andreas
Lesche, Mathias
Boye, Susanne
Lederer, Albena
Shih, William M.
A smart polymer for sequence-selective binding, pulldown, and release of DNA targets
title A smart polymer for sequence-selective binding, pulldown, and release of DNA targets
title_full A smart polymer for sequence-selective binding, pulldown, and release of DNA targets
title_fullStr A smart polymer for sequence-selective binding, pulldown, and release of DNA targets
title_full_unstemmed A smart polymer for sequence-selective binding, pulldown, and release of DNA targets
title_short A smart polymer for sequence-selective binding, pulldown, and release of DNA targets
title_sort smart polymer for sequence-selective binding, pulldown, and release of dna targets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351716/
https://www.ncbi.nlm.nih.gov/pubmed/32651444
http://dx.doi.org/10.1038/s42003-020-1082-2
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