Many nanosensors require a target molecule to bind simultaneously to multiple receptors, limiting sensitivity and excluding small or single-epitope analytes. This technology uses a single binding event to mechanically restrict the movement of a nanoscale structure. The resulting change can be detected optically, by fluorescence, FRET or surface plasmon resonance.
Physical Sciences
Diagnostics
Reference
b82065
IP right year
2024
IP status
EP and US filed
Applicant
Technical University of Munich
Contact
Nicola Hoesch

Challenge and innovation

Conventional nanosensors often rely on dual-receptor or sandwich architectures. Detection therefore requires sufficiently large molecules with two suitable binding sites, such as two epitopes. Small molecules, nucleic acids or single-epitope targets may not generate a sufficient signal. In addition, many existing sensors measure intensity changes rather than directly resolving the molecular motion underlying the detection event.

The technology introduces a mechanically responsive nanosensor in which one binding structure per joint is sufficient to generate a detectable signal. Target binding changes or limits the destruction-free mobility between two nanostructures, for example by blocking a hinge or reducing a defined rotation angle. DNA origami can be used to precisely position the structures, hinges, receptors and optical labels. Detection is possible through single-molecule fluorescence tracking, FRET or surface plasmon resonance, enabling flexible sensor formats for different analytes and readout platforms.

Talk to an expert

Interested in learning more about this technology offer, exploring potential applications or discussing a possible collaboration? Get in touch to learn more.

Nicola Hoesch