On-chip conductometric detection of short DNA sequences via electro-hydrodynamic aggregation
Creators
Abstract
Fluorescence measurement is the main technology for post-amplification DNA detection in automated systems. Direct electrical reading of DNA concentration in solution could be an interesting alternative to go toward more miniaturized or less expensive devices, in particular in the pathogen detection field. Here we present the detection of short bacterial biomarkers with a direct impedancemetric measurement, within solutions of amplified and elongated DNA sequences in a microchannel. This technology relies on the electrohydrodynamic instability occurring in solutions of long charged macromolecules in a strong electric field. This instability specifically induces the aggregation of long DNAs and triggers conductivity variations that can be monitored by on-contact conductometry. An innovative isothermal amplification and elongation strategy was developed, combining SDA and HRCA reactions, in order to yield long DNAs suitable to be detected by the above principle, from a dilute initial DNA target. In contrast with previous label-free detection methods, this new strategy is very robust to matrix effects, thanks to the unique molecular weight dependence of the instability, coupled with this specific DNA amplification strategy. We demonstrate the detection of a 1 pM gene sequence specific to Staphylococcus aureus, in a portable system.
Additional Information
© 2018 The Royal Society of Chemistry. Submitted 13 May 2017; Accepted 02 Nov 2017; First published 24 Nov 2017. We thank Robert Breton for assistance in the electronic development, P. Silberzan and A. Buguin for access to the clean room of the Curie Institute and Jérôme Champ for biological support. Our gratitude also goes to Mats Nilsson (Science for Life Laboratory, Stockholm University) for fruitful discussion and help on the DNA amplification scheme. This work has received the support of Institut Pierre-Gilles de Gennes (équipement d'excellence, "Investissements d'avenir", program ANR-10-EQPX-34). This work was supported by a Direction Générale de l'Armement (DGA) PhD fellowship to BV and by the ERC Advanced Grant CellO (FP7-IDEAS-ERC-321107). Some authors are coinventors of patent WO2014006561 to CNRS and Institut Curie.Attached Files
Supplemental Material - c7an00798a1.pdf
Files
c7an00798a1.pdf
Additional details
Identifiers
- Eprint ID
- 107052
- DOI
- 10.1039/c7an00798a
- Resolver ID
- CaltechAUTHORS:20201214-072223959
Related works
- Describes
- 10.1039/c7an00798a (DOI)
Funding
- Institut Pierre-Gilles de Gennes
- Agence Nationale pour la Recherche (ANR)
- ANR-10-EQPX-34
- European Research Council (ERC)
- 321107
Dates
- Created
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2020-12-14Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field