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DNA Origami Vesicle Sensors with Triggered Cargo Transfer

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ABSTRACTInteracting 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. Leveraging the programmable nature of DNA origami, we engineered a biosensor harnessing single-molecule Fluorescence Resonance Energy Transfer (smFRET) as transduction mechanism for precise lipid vesicle detection. The system hinges on a hydrophobic ATTO647N modified single-stranded DNA (ssDNA) leash, protruding from a rectangular DNA origami. In a vesicle-free environment, the ssDNA adopts a coiled stance, ensuring high FRET efficiency. However, upon lipid vesicle binding to cholesterol anchors on the DNA origami, the hydrophobic ATTO647N induces the ssDNA to stretch towards the lipid bilayer, leading to reduced FRET efficiency. The strategic placement of cholesterol anchors further modulates this interaction, affecting the observed FRET populations. Beyond its role as a vesicle sensor, we show targeted cargo transport of the acceptor dye unit to the vesicle. The cargo transport is initiated by vesicle bound DNA and a strand displacement reaction. Our interaction platform opens pathways for innovative interaction such as biosensing and molecular transport with complex biosystems.
Title: DNA Origami Vesicle Sensors with Triggered Cargo Transfer
Description:
ABSTRACTInteracting 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.
Leveraging the programmable nature of DNA origami, we engineered a biosensor harnessing single-molecule Fluorescence Resonance Energy Transfer (smFRET) as transduction mechanism for precise lipid vesicle detection.
The system hinges on a hydrophobic ATTO647N modified single-stranded DNA (ssDNA) leash, protruding from a rectangular DNA origami.
In a vesicle-free environment, the ssDNA adopts a coiled stance, ensuring high FRET efficiency.
However, upon lipid vesicle binding to cholesterol anchors on the DNA origami, the hydrophobic ATTO647N induces the ssDNA to stretch towards the lipid bilayer, leading to reduced FRET efficiency.
The strategic placement of cholesterol anchors further modulates this interaction, affecting the observed FRET populations.
Beyond its role as a vesicle sensor, we show targeted cargo transport of the acceptor dye unit to the vesicle.
The cargo transport is initiated by vesicle bound DNA and a strand displacement reaction.
Our interaction platform opens pathways for innovative interaction such as biosensing and molecular transport with complex biosystems.

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