High-Throughput Synthesis and Screening of Functional Coacervates Using Microfluidics

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Thomas Beneyton - , Université de Bordeaux (Autor:in)
  • Celina Love - , Exzellenzcluster PoL: Physik des Lebens, Professur für BioNano-Werkzeuge, Max Planck Institute of Molecular Cell Biology and Genetics, Technische Universität Dresden (Autor:in)
  • Mathias Girault - , Université de Bordeaux (Autor:in)
  • T. Y.Dora Tang - , Max Planck Institute of Molecular Cell Biology and Genetics, Technische Universität Dresden, Exzellenzcluster PoL: Physik des Lebens (Autor:in)
  • Jean Christophe Baret - , Université de Bordeaux, Institut universitaire de France (Autor:in)

Abstract

To understand how membrane-free subcompartmentalization can modulate biochemical reactions by coupled spatial enzyme localization with substrate and product partitioning, we use microfluidic strategies to synthesize, stabilize and characterize micron-sized functional coacervates in water−oil emulsions. Our methodologies have allowed for the first time to quantitatively characterize partition coefficients of a broad range of different molecules with different coacervate chemistries and to measure reaction rates of individual subcompartments and their surrounding aqueous environment at the single coacervate level. Our results show that sub-compartmentalisation increases the overall rates of reactions. This bottom-up synthetic strategy for the production of synthetic organelles offers a physical model for membrane-free compartmentalization in biology and provides insights into the role of sub-compartmentalisation in regulating out-of-equilibrium behaviours in biological systems.

Details

OriginalspracheEnglisch
Aufsatznummere2000022
FachzeitschriftChemSystemsChem
Jahrgang2
Ausgabenummer6
PublikationsstatusVeröffentlicht - Nov. 2020
Peer-Review-StatusJa

Schlagworte

Schlagwörter

  • coacervates, microfluidics, out-of-equilibrium, soft matter, synthetic chemistry