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Artificial cell synthesis using biocatalytic polymerization-induced self-assembly

Andrea Belluati, Sètuhn Jimaja, Robert J. Chadwick, Christopher Glynn, Mohamed Chami, Dominic Happel, Chao Guo, Harald Kolmar, Nico Bruns*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Artificial cells are biomimetic microstructures that mimic functions of natural cells, can be applied as building blocks for molecular systems engineering, and host synthetic biology pathways. Here we report enzymatically synthesized polymer-based artificial cells with the ability to express proteins. Artificial cells were synthesized using biocatalytic atom transfer radical polymerization-induced self-assembly, in which myoglobin synthesizes amphiphilic block co-polymers that self-assemble into structures such as micelles, worm-like micelles, polymersomes and giant unilamellar vesicles (GUVs). The GUVs encapsulate cargo during the polymerization, including enzymes, nanoparticles, microparticles, plasmids and cell lysate. The resulting artificial cells act as microreactors for enzymatic reactions and for osteoblast-inspired biomineralization. Moreover, they can express proteins such as a fluorescent protein and actin when fed with amino acids. Actin polymerizes in the vesicles and alters the artificial cells’ internal structure by creating internal compartments. Thus, biocatalytic atom transfer radical polymerization-induced self-assembly-derived GUVs can mimic bacteria as they are composed of a microscopic reaction compartment that contains genetic information for protein expression upon induction.
Original languageEnglish
Pages (from-to)564-574
Number of pages11
JournalNature Chemistry
Volume16
Issue number4
Early online date4 Dec 2023
DOIs
Publication statusPublished - 1 Apr 2024

Funding

This research was supported by the Swiss National Science Foundation through the National Centre of Competence in Research (NCCR) Bio-Inspired Materials (grant no. 51NF40–182881, S.J., N.B.), and has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement no. 101032493 (A.B.). Furthermore, this work was supported by PhD fellowships of the University of Strathclyde to C.G. and R.J.C., as well as by the UK Engineering and Physical Sciences Research Council (grant numbers EP/V047035/1 and EP/V047035/2). The authors wish to thank A. M. Moreno-Echeverri and A. Petri-Fink (Adolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland) for providing the SiO NPs. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript 2

Keywords

  • molecular self-assembly
  • nanoscale materials
  • chemical origin of life
  • polymer synthesis
  • synthetic biology

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