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Purification of DNA-origami nanostructures by rate-zonal centrifugation
Most previously reported methods for purifying DNA-origami nanostructures rely on agarose-gel electrophoresis (AGE) for separation. Although AGE is routinely used to yield 0.1–1 µg purified DNA nanostructures, obtaining >100 µg of purified DNA-origami structure through AGE is typically laborious...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553994/ https://www.ncbi.nlm.nih.gov/pubmed/23155067 http://dx.doi.org/10.1093/nar/gks1070 |
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author | Lin, Chenxiang Perrault, Steven D. Kwak, Minseok Graf, Franziska Shih, William M. |
author_facet | Lin, Chenxiang Perrault, Steven D. Kwak, Minseok Graf, Franziska Shih, William M. |
author_sort | Lin, Chenxiang |
collection | PubMed |
description | Most previously reported methods for purifying DNA-origami nanostructures rely on agarose-gel electrophoresis (AGE) for separation. Although AGE is routinely used to yield 0.1–1 µg purified DNA nanostructures, obtaining >100 µg of purified DNA-origami structure through AGE is typically laborious because of the post-electrophoresis extraction, desalting and concentration steps. Here, we present a readily scalable purification approach utilizing rate-zonal centrifugation, which provides comparable separation resolution as AGE. The DNA nanostructures remain in aqueous solution throughout the purification process. Therefore, the desired products are easily recovered with consistently high yield (40–80%) and without contaminants such as residual agarose gel or DNA intercalating dyes. Seven distinct three-dimensional DNA-origami constructs were purified at the scale of 0.1–100 µg (final yield) per centrifuge tube, showing the versatility of this method. Given the commercially available equipment for gradient mixing and fraction collection, this method should be amenable to automation and further scale up for preparation of larger amounts (e.g. milligram quantities) of DNA nanostructures. |
format | Online Article Text |
id | pubmed-3553994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35539942013-01-24 Purification of DNA-origami nanostructures by rate-zonal centrifugation Lin, Chenxiang Perrault, Steven D. Kwak, Minseok Graf, Franziska Shih, William M. Nucleic Acids Res Methods Online Most previously reported methods for purifying DNA-origami nanostructures rely on agarose-gel electrophoresis (AGE) for separation. Although AGE is routinely used to yield 0.1–1 µg purified DNA nanostructures, obtaining >100 µg of purified DNA-origami structure through AGE is typically laborious because of the post-electrophoresis extraction, desalting and concentration steps. Here, we present a readily scalable purification approach utilizing rate-zonal centrifugation, which provides comparable separation resolution as AGE. The DNA nanostructures remain in aqueous solution throughout the purification process. Therefore, the desired products are easily recovered with consistently high yield (40–80%) and without contaminants such as residual agarose gel or DNA intercalating dyes. Seven distinct three-dimensional DNA-origami constructs were purified at the scale of 0.1–100 µg (final yield) per centrifuge tube, showing the versatility of this method. Given the commercially available equipment for gradient mixing and fraction collection, this method should be amenable to automation and further scale up for preparation of larger amounts (e.g. milligram quantities) of DNA nanostructures. Oxford University Press 2013-01 2012-11-15 /pmc/articles/PMC3553994/ /pubmed/23155067 http://dx.doi.org/10.1093/nar/gks1070 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com. |
spellingShingle | Methods Online Lin, Chenxiang Perrault, Steven D. Kwak, Minseok Graf, Franziska Shih, William M. Purification of DNA-origami nanostructures by rate-zonal centrifugation |
title | Purification of DNA-origami nanostructures by rate-zonal centrifugation |
title_full | Purification of DNA-origami nanostructures by rate-zonal centrifugation |
title_fullStr | Purification of DNA-origami nanostructures by rate-zonal centrifugation |
title_full_unstemmed | Purification of DNA-origami nanostructures by rate-zonal centrifugation |
title_short | Purification of DNA-origami nanostructures by rate-zonal centrifugation |
title_sort | purification of dna-origami nanostructures by rate-zonal centrifugation |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553994/ https://www.ncbi.nlm.nih.gov/pubmed/23155067 http://dx.doi.org/10.1093/nar/gks1070 |
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