Controlled deprotection and release of a small molecule from a compartmented synthetic tissue module

Synthetic tissues built from communicating aqueous droplets offer potential applications in biotechnology, however, controlled release of their contents has not been achieved. Here we construct two-droplet synthetic tissue modules that function in an aqueous environment. One droplet contains a cell-...

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Veröffentlicht in:Communications chemistry 2019-12, Vol.2 (1), Article 142
Hauptverfasser: Booth, Michael J., Cazimoglu, Idil, Bayley, Hagan
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Sprache:eng
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Zusammenfassung:Synthetic tissues built from communicating aqueous droplets offer potential applications in biotechnology, however, controlled release of their contents has not been achieved. Here we construct two-droplet synthetic tissue modules that function in an aqueous environment. One droplet contains a cell-free protein synthesis system and a prodrug-activating enzyme and the other a small-molecule prodrug analog. When a Zn 2+ -sensitive protein pore is made in the first droplet, it allows the prodrug to migrate from the second droplet and become activated by the enzyme. With Zn 2+ in the external medium, the activated molecule is retained in the module until it is released on-demand by a divalent cation chelator. The module is constructed in such a manner that one or more, potentially with different properties, might be incorporated into extended synthetic tissues, including patterned materials generated by 3D-printing. Such modules will thereby increase the sophistication of synthetic tissues for applications including controlled multidrug delivery. Droplet networks capable of transporting molecules between compartments can function as tissue-like materials. Here an encapsulated transcription/translation system generates a Zn-controlled membrane pore, which allows interdroplet transport, enzymatic deprotection and controlled release of a small molecule to the external environment.
ISSN:2399-3669
2399-3669
DOI:10.1038/s42004-019-0244-y