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Synthetic Condensates and Cell-Like Architectures from Amphiphilic DNA Nanostructures.
Malouf, Layla; Tanase, Diana A; Di Michele, Lorenzo.
Affiliation
  • Malouf L; Department of Chemical Engineering and Biotechnology, University of Cambridge; Department of Chemistry, Imperial College London.
  • Tanase DA; Department of Chemical Engineering and Biotechnology, University of Cambridge; Department of Chemistry, Imperial College London.
  • Di Michele L; Department of Chemical Engineering and Biotechnology, University of Cambridge; Department of Chemistry, Imperial College London; fabriCELL, Imperial College London; ld389@cam.c.uk.
J Vis Exp ; (207)2024 May 31.
Article in En | MEDLINE | ID: mdl-38884477
ABSTRACT
Synthetic droplets and condensates are becoming increasingly common constituents of advanced biomimetic systems and synthetic cells, where they can be used to establish compartmentalization and sustain life-like responses. Synthetic DNA nanostructures have demonstrated significant potential as condensate-forming building blocks owing to their programmable shape, chemical functionalization, and self-assembly behavior. We have recently demonstrated that amphiphilic DNA "nanostars", obtained by labeling DNA junctions with hydrophobic moieties, constitute a particularly robust and versatile solution. The resulting amphiphilic DNA condensates can be programmed to display complex, multi-compartment internal architectures, structurally respond to various external stimuli, synthesize macromolecules, capture and release payloads, undergo morphological transformations, and interact with live cells. Here, we demonstrate protocols for preparing amphiphilic DNA condensates starting from constituent DNA oligonucleotides. We will address (i) single-component systems forming uniform condensates, (ii) two-component systems forming core-shell condensates, and (iii) systems in which the condensates are modified to support in vitro transcription of RNA nanostructures.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Nanostructures Language: En Journal: J Vis Exp Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Nanostructures Language: En Journal: J Vis Exp Year: 2024 Document type: Article Country of publication: United States