Reversible pH-Responsive Coacervate Formation in Lipid Vesicles Activates Dormant Enzymatic Reactions

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Celina Love - , Clusters of Excellence PoL: Physics of Life, Chair of BioNano-Tools, Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Jan Steinkühler - , Max Planck Institute of Colloids and Interfaces (Author)
  • David T. Gonzales - , Clusters of Excellence PoL: Physics of Life, Chair of Applied Genomics, Max Planck Institute of Molecular Cell Biology and Genetics, Center for Systems Biology Dresden (CSBD) (Author)
  • Naresh Yandrapalli - , Max Planck Institute of Colloids and Interfaces (Author)
  • Tom Robinson - , Max Planck Institute of Colloids and Interfaces (Author)
  • Rumiana Dimova - , Max Planck Institute of Colloids and Interfaces (Author)
  • T. Y.Dora Tang - , Max Planck Institute of Molecular Cell Biology and Genetics, TUD Dresden University of Technology, Clusters of Excellence PoL: Physics of Life (Author)

Abstract

In situ, reversible coacervate formation within lipid vesicles represents a key step in the development of responsive synthetic cellular models. Herein, we exploit the pH responsiveness of a polycation above and below its pKa, to drive liquid–liquid phase separation, to form single coacervate droplets within lipid vesicles. The process is completely reversible as coacervate droplets can be disassembled by increasing the pH above the pKa. We further show that pH-triggered coacervation in the presence of low concentrations of enzymes activates dormant enzyme reactions by increasing the local concentration within the coacervate droplets and changing the local environment around the enzyme. In conclusion, this work establishes a tunable, pH responsive, enzymatically active multi-compartment synthetic cell. The system is readily transferred into microfluidics, making it a robust model for addressing general questions in biology, such as the role of phase separation and its effect on enzymatic reactions using a bottom-up synthetic biology approach.

Details

Original languageEnglish
Pages (from-to)5950-5957
Number of pages8
JournalAngewandte Chemie - International Edition
Volume59
Issue number15
Publication statusPublished - 6 Apr 2020
Peer-reviewedYes

External IDs

PubMed 31943629

Keywords

ASJC Scopus subject areas

Keywords

  • coacervates, liquid–liquid phase separation, microfluidics, pH responsive, protocells