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DNA Origami Seesaws as Comparative Binding Assay

The application of commonly used force spectroscopy in biological systems is often limited by the need for an invasive tether connecting the molecules of interest to a bead or cantilever tip. Here we present a DNA origami‐based prototype in a comparative binding assay. It has the advantage of in sit...

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Autores principales: Nickels, Philipp C., Høiberg, Hans C., Simmel, Stephanie S., Holzmeister, Phil, Tinnefeld, Philip, Liedl, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084756/
https://www.ncbi.nlm.nih.gov/pubmed/27038073
http://dx.doi.org/10.1002/cbic.201600059
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author Nickels, Philipp C.
Høiberg, Hans C.
Simmel, Stephanie S.
Holzmeister, Phil
Tinnefeld, Philip
Liedl, Tim
author_facet Nickels, Philipp C.
Høiberg, Hans C.
Simmel, Stephanie S.
Holzmeister, Phil
Tinnefeld, Philip
Liedl, Tim
author_sort Nickels, Philipp C.
collection PubMed
description The application of commonly used force spectroscopy in biological systems is often limited by the need for an invasive tether connecting the molecules of interest to a bead or cantilever tip. Here we present a DNA origami‐based prototype in a comparative binding assay. It has the advantage of in situ readout without any physical connection to the macroscopic world. The seesaw‐like structure has a lever that is able to move freely relative to its base. Binding partners on each side force the structure into discrete and distinguishable conformations. Model experiments with competing DNA hybridisation reactions yielded a drastic shift towards the conformation with the stronger binding interaction. With reference DNA duplexes of tuneable length on one side, this device can be used to measure ligand interactions in comparative assays.
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spelling pubmed-50847562016-11-09 DNA Origami Seesaws as Comparative Binding Assay Nickels, Philipp C. Høiberg, Hans C. Simmel, Stephanie S. Holzmeister, Phil Tinnefeld, Philip Liedl, Tim Chembiochem Communications The application of commonly used force spectroscopy in biological systems is often limited by the need for an invasive tether connecting the molecules of interest to a bead or cantilever tip. Here we present a DNA origami‐based prototype in a comparative binding assay. It has the advantage of in situ readout without any physical connection to the macroscopic world. The seesaw‐like structure has a lever that is able to move freely relative to its base. Binding partners on each side force the structure into discrete and distinguishable conformations. Model experiments with competing DNA hybridisation reactions yielded a drastic shift towards the conformation with the stronger binding interaction. With reference DNA duplexes of tuneable length on one side, this device can be used to measure ligand interactions in comparative assays. John Wiley and Sons Inc. 2016-05-06 2016-06-16 /pmc/articles/PMC5084756/ /pubmed/27038073 http://dx.doi.org/10.1002/cbic.201600059 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Nickels, Philipp C.
Høiberg, Hans C.
Simmel, Stephanie S.
Holzmeister, Phil
Tinnefeld, Philip
Liedl, Tim
DNA Origami Seesaws as Comparative Binding Assay
title DNA Origami Seesaws as Comparative Binding Assay
title_full DNA Origami Seesaws as Comparative Binding Assay
title_fullStr DNA Origami Seesaws as Comparative Binding Assay
title_full_unstemmed DNA Origami Seesaws as Comparative Binding Assay
title_short DNA Origami Seesaws as Comparative Binding Assay
title_sort dna origami seesaws as comparative binding assay
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084756/
https://www.ncbi.nlm.nih.gov/pubmed/27038073
http://dx.doi.org/10.1002/cbic.201600059
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