Research Article
An autonomously self-assembling dendritic DNA nanostructure for target DNA detection
Article first published online: 10 OCT 2012
DOI: 10.1002/biot.201100499
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Biotechnology Journal
Special Issue: Nanobio vs. Bionano
Volume 8, Issue 2, pages 221–227, February 2013
Additional Information
How to Cite
Chandran, H., Rangnekar, A., Shetty, G., Schultes, E. A., Reif, J. H. and LaBean, T. H. (2013), An autonomously self-assembling dendritic DNA nanostructure for target DNA detection. Biotechnology Journal, 8: 221–227. doi: 10.1002/biot.201100499
Publication History
- Issue published online: 5 FEB 2013
- Article first published online: 10 OCT 2012
- Accepted manuscript online: 11 SEP 2012 01:40AM EST
- Manuscript Accepted: 6 SEP 2012
- Manuscript Revised: 9 AUG 2012
- Manuscript Received: 25 APR 2012
Funded by
- NSF. Grant Number: CCF-1141847, CCF 0829749
- NSF EMT. Grant Number: CCF-0829797, CCF-0829798
- AFSOR Contract. Grant Number: FA9550-08-1-0188
Keywords:
- DNA sequence detection;
- Hybridization cascade;
- Molecular self-assembly;
- Nanobiotechnology;
- Nucleic acids
Abstract
There is a growing need for sensitive and reliable nucleic acid detection methods that are convenient and inexpensive. Responsive and programmable DNA nanostructures have shown great promise as chemical detection systems. Here, we describe a DNA detection system employing the triggered self-assembly of a novel DNA dendritic nanostructure. The detection protocol is executed autonomously without external intervention. Detection begins when a specific, single-stranded target DNA strand (T) triggers a hybridization chain reaction (HCR) between two, distinct DNA hairpins (α and β). Each hairpin opens and hybridizes up to two copies of the other. In the absence of T, α and β are stable and remain in their poised, closed-hairpin form. In the presence of T, α hairpins are opened by toe-hold mediated strand-displacement, each of which then opens and hybridizes two β hairpins. Likewise, each opened β hairpin can open and hybridize two α hairpins. Hence, each layer of the growing dendritic nanostructure can in principle accommodate an exponentially increasing number of cognate molecules, generating a high molecular weight nanostructure. This HCR system has minimal sequence constraints, allowing reconfiguration for the detection of arbitrary target sequences. Here, we demonstrate detection of unique sequence identifiers of HIV and Chlamydia pathogens.

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