2013 journal article

An autonomously self-assembling dendritic DNA nanostructure for target DNA detection

BIOTECHNOLOGY JOURNAL, 8(2), 221–227.

By: H. Chandran*, A. Rangnekar n, G. Shetty*, E. Schultes*, J. Reif* & T. LaBean n

co-author countries: Netherlands 🇳🇱 United States of America 🇺🇸
author keywords: DNA sequence detection; Hybridization cascade; Molecular self-assembly; Nanobiotechnology; Nucleic acids
MeSH headings : Biosensing Techniques / instrumentation; Biosensing Techniques / methods; Chlamydia / isolation & purification; DNA / chemistry; DNA / isolation & purification; Electrophoresis, Polyacrylamide Gel; Gold / chemistry; HIV / isolation & purification; Metal Nanoparticles / chemistry; Nucleic Acid Conformation; Nucleic Acid Hybridization; Sequence Analysis, DNA / methods
Source: Web Of Science
Added: August 6, 2018

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.