Characterization and optimization of vesicle properties in bioPISA: from size distribution to post-assembly loading

Andrea Belluati*, Adrian Bloch, Kaloian Koynov, Mariana Müller Nieva, Mohadeseh Bagherabadi, Annette Andrieu-Brunsen, Harald Kolmar, Nico Bruns*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

This study investigates the formation and properties of vesicles produced via biocatalytic Polymerization-Induced Self-Assembly (bioPISA) as artificial cells. Methods for achieving size uniformity, including gentle centrifugation and sucrose gradient centrifugation, are explored, and the effects of stirring speed on vesicle morphology is investigated. The internal structure of the vesicles, characterized by a polymer-rich matrix, is analyzed using fluorescence correlation spectroscopy (FCS). Additionally, the feasibility of loading macromolecules into pre-formed vesicles is demonstrated using electroporation, and a fluorescent protein as well as enzymes for a cascade reaction were sucesfully incorporated into the fully assembled polymersomes. These findings provide a foundation for developing enzyme-synthesized polymeric vesicles with controlled morphologies for various applications, e.g., in synthetic biology.
Original languageEnglish
Article number2400483
Number of pages9
JournalAdvanced Biology
Early online date18 Dec 2024
DOIs
Publication statusE-pub ahead of print - 18 Dec 2024

Funding

This research was supported by the European Union's Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement no. 101032493, the TU Darmstadt Athene Young Investigator Program, and the CoM42Life Pathfinder funding.

Keywords

  • enzymatic polymerization
  • PISA
  • polymersomes
  • artificial cells

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