PDOC - Retour Postdoctorants 2013

Digital DNA nano arrays – DigiNANO

DigiNano

Digital DNA nanoarrays

Challenge: placing DNA nanostructures with nanometer precision over large surfaces

This project aims at combining DNA nanotechnology and top-down nanofabrication to pattern DNA nanostructures over large areas with nanometer precision. It is expected that these structures will allow the detection of biological DNA and RNA with single-molecule precision and high-throughput.

This project combines e-beam lithography and DNA nanotechnology.

The electron beam lithography is used to define zones of about 100 nm, which will then be functionalized to graft DNA nanostructures such as DNA origamis. These nanostructures bear DNA strands that are programmed to capture DNA targets and amplify the corresponding signal to be read by a fluorescence microscope .

Due to the transfer of the principal investigator to LIMMS, and in the absence of the concomitant transfer of this grant to LIMMS, no significant results can be reported.

It is difficult to provide a perspective due to the effective stopping of the project after 8 months.

High-resolution mapping of bifurcations in nonlinear biochemical circuits, A. J. Genot, A. Baccouche, R. Sieskind, N. Aubert-Kato, N. Bredeche, J. F. Bartolo, V. Taly, T. Fujii & Y. Rondelez, Nature Chemistry (2016)

Controlling the placement of molecules on large surfaces with nanometer precision is a common goal of photonic, electronic and biosensing. Top-down fabrication (through lithography, deposition and etching) has been a very successful technology to shape matter from the centimeter down to the 100-nm range. Yet, as the technology is pushed further down, it becomes prohibitively expensive to overcome the limitation of diffraction and reach for the 1-100 nm range. Bottom-up assembly is a perfect technology to bridge this gap. Inspired by the robustness and precision of self-assembled biological structures, bottom-up assembly relies on the programmed self-assembly of atoms and molecules to build large complexes (10-100nm) from simple bricks (0.1-1nm). Top-down and bottom-up assembly hold together the potential to tailor the properties of materials down to the atomic scales, thus enabling tremendous new applications.

I propose to combine bottom-up and top-down assembly, coupled to single-molecule microscopy and microfluidics, in order to address technological locks in the quantification of biomolecules. By arranging biomolecules with nanometer precision on square millimeter surfaces, we aim to build digital arrays that count digitally many distinct targets, with high sensitivity, high specificity, minimal operations and high reliability. Because the array will be developed with potential applications in mind, a particular emphasis will be placed on robustness, reproducibility and integration.

Project coordination

Anthony GENOT (Laboratoire d'Analyse et d'Architecture des Systèmes)

The author of this summary is the project coordinator, who is responsible for the content of this summary. The ANR declines any responsibility as for its contents.

Partnership

LAAS Laboratoire d'Analyse et d'Architecture des Systèmes

Help of the ANR 420,000 euros
Beginning and duration of the scientific project: February 2014 - 42 Months

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