DNA Origami Vesicle Sensors with Triggered Single‐Molecule Cargo Transfer

Abstract Interacting with living systems typically involves the ability to address lipid membranes of cellular systems. The first step of interaction of a nanorobot with a cell will thus be the detection of binding to a lipid membrane. Utilizing DNA origami, we engineered a biosensor with single‐molecule Fluorescence Resonance Energy Transfer (smFRET) as transduction mechanism for precise lipid vesicle detection and cargo delivery. The system hinges on a hydrophobic ATTO647N modified single‐stranded DNA (ssDNA) leash, protruding from a DNA origami nanostructure. In a vesicle‐free environment, the ssDNA coils, ensuring high FRET efficiency. Upon vesicle binding to cholesterol anchors on the DNA origami, hydrophobic ATTO647N induces the ssDNA to stretch towards the lipid bilayer, reducing FRET efficiency. As the next step, the sensing strand serves as molecular cargo that can be transferred to the vesicle through a triggered strand displacement reaction. Depending on the number of cholesterols on the displacer strands, we either induce a diffusive release of the fluorescent load towards neighboring vesicles or a stoichiometric release of a single cargo‐unit to the vesicle on the nanosensor. Ultimately, our multi‐functional liposome interaction and detection platform opens up pathways for innovative biosensing applications and stoichiometric loading of vesicles with single‐molecule control.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2024-09-09
DOI
https://doi.org/10.1002/anie.202408295
Citations
6
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
1.40

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article

DNA Origami Vesicle Sensors with Triggered Single‐Molecule Cargo Transfer

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6 citations
Angewandte Chemie International Edition
Advanced biosensing and bioanalysis techniques
1.40
article

DNA Origami Vesicle Sensors with Triggered Single‐Molecule Cargo Transfer

Renukka Yaadav, Tim Schröder, Henri G. Franquelim, Philip Tinnefeld, Ece Büber
article en
6 citations

Abstract

Abstract Interacting with living systems typically involves the ability to address lipid membranes of cellular systems. The first step of interaction of a nanorobot with a cell will thus be the detection of binding to a lipid membrane. Utilizing DNA origami, we engineered a biosensor with single‐molecule Fluorescence Resonance Energy Transfer (smFRET) as transduction mechanism for precise lipid vesicle detection and cargo delivery. The system hinges on a hydrophobic ATTO647N modified single‐stranded DNA (ssDNA) leash, protruding from a DNA origami nanostructure. In a vesicle‐free environment, the ssDNA coils, ensuring high FRET efficiency. Upon vesicle binding to cholesterol anchors on the DNA origami, hydrophobic ATTO647N induces the ssDNA to stretch towards the lipid bilayer, reducing FRET efficiency. As the next step, the sensing strand serves as molecular cargo that can be transferred to the vesicle through a triggered strand displacement reaction. Depending on the number of cholesterols on the displacer strands, we either induce a diffusive release of the fluorescent load towards neighboring vesicles or a stoichiometric release of a single cargo‐unit to the vesicle on the nanosensor. Ultimately, our multi‐functional liposome interaction and detection platform opens up pathways for innovative biosensing applications and stoichiometric loading of vesicles with single‐molecule control.

Angewandte Chemie International EditionVol. 63(49)
Center for NanoScience (DE), Ludwig-Maximilians-Universität München (DE), Leipzig University (DE)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Sächsisches Staatsministerium für Wissenschaft und Kunst, Bundesministerium für Wirtschaft und Energie
Affordable and clean energy
Openalex Percentile: Top 19%
Advanced biosensing and bioanalysis techniques
1.40
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