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Dynamic actuation of DNA-assembled plasmonic nanostructures in microfluidic cell-sized compartments

DOI:10.1021/acs.nanolett.9b04217 期刊:Nano Letters 出版年份:2020 更新时间:2025-09-23 15:19:57
摘要: Molecular motor proteins form the basis of cellular dynamics. Recently, notable efforts have led to the creation of their DNA-based mimics, which can carry out complex nanoscale motion. However, such functional analogues have not yet been integrated or operated inside synthetic cells towards the goal of realizing artificial biological systems entirely from the bottom-up. In this Letter, we encapsulate and actuate DNA-assembled dynamic nanostructures inside cell-sized microfluidic compartments. These encapsulated DNA nanostructures not only exhibit structural reconfigurability owing to their pH-sensitive molecular switches upon external stimuli, but also possess optical feedback enabled by the integrated plasmonic probes. In particular, we demonstrate the power of microfluidic compartmentalization for achieving on-chip plasmonic enantiomer separation and substrate filtration. Our work exemplifies that the two unique tools, droplet-based microfluidics and DNA technology, offering high precision on the microscale and nanoscale, respectively, can be brought together to greatly enrich the complexity and diversity of functional synthetic systems.
作者: Kerstin G?pfrich,Maximilian J. Urban,Christoph Frey,Ilia Platzman,Joachim P. Spatz,Na Liu
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The futuristic objective of synthetic biology is to build artificial systems such as synthetic cells, in which different functional entities can be designed and constructed entirely from the bottom-up. Progress towards this objective requires inspiring strategies to combine and arrange a multitude of functional building blocks in space and time.

The study demonstrates how the combination of precision technologies – DNA nanotechnology and droplet-based microfluidics – provides new possibilities to construct, operate and monitor artificial dynamic nanostructures inside synthetic cells. It proves their reversible pH-triggered reconfiguration by CD spectroscopy, TEM and confocal fluorescence imaging. The work opens up promising potential for future work featuring the realization of stimulus cascades, mimicking reaction pathways in living cells.

The technical and application constraints include the challenges in protein purification and the argument that a truly synthetic cell should contain solely man-made components. Potential areas for optimization include the integration of more complex functions and the improvement of the stability and efficiency of the DNA nanostructures.

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