We report on the formation of coacervate droplets from poly(diallyldimethylammonium chloride) with either adenosine triphosphate or carboxymethyl-dextran using a microfluidic flow-focusing system. The formed droplets exhibit improved stability and narrower size distributions for both coacervate compositions when compared to the conventional vortex dispersion techniques. We also demonstrate the use of two parallel flow-focusing channels for the simultaneous formation and co-location of two distinct populations of coacervate droplets containing different DNA oligonucleotides, and that the populations can coexist in close proximity up to 48 h without detectable exchange of genetic information. Our results show that the observed improvements in droplet stability and size distribution may be scaled with ease. In addition, the ability to encapsulate different materials into coacervate droplets using a microfluidic channel structure allows for their use as cell-mimicking compartments.
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http://dx.doi.org/10.1002/anie.201502886 | DOI Listing |
ACS Nano
December 2024
Department of Biomedical Engineering, City University of Hong Kong, Y6700, 6/F, Yellow Zone, Yeung Kin Man Academic Building, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China.
The development of membrane-bound protocells, which process cascade biochemical reactions in distinct microcompartments, marks a significant advancement in soft systems. However, many synthesized protocells with cell membrane-like structures are prone to rupturing in biological environments and are challenging to functionalize, limiting their biomedical applications. In this study, we explore the liquid-liquid phase separation of tannic acid (TA) and polyethylene glycol (PEG) to form coacervate droplets.
View Article and Find Full Text PDFMacromol Rapid Commun
December 2024
Department of Physical Chemistry of Polymers, Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
J Mater Chem B
November 2024
New Chemistry Unit and School of Advanced Materials (SAMat), Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Bangalore 560064, India.
Phase separation and phase transitions pervade the biological domain, where proteins and RNA engage in liquid-liquid phase separation (LLPS), forming liquid-like membraneless organelles. The misregulation or dysfunction of these proteins culminates in the formation of solid aggregates a liquid-to-solid transition, leading to pathogenic conditions. To decipher the underlying mechanisms, synthetic LLPS has been examined through complex coacervate formation from charged polymers.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
MPIP: Max-Planck-Institut fur Polymerforschung, Department of physical chemistry, GERMANY.
Liquid-liquid phase separation towards the formation of synthetic coacervate droplets represents a rapidly advancing frontier in the fields of synthetic biology, material science, and biomedicine. These artificial constructures mimic the biophysical principles and dynamic features of natural biomolecular condensates that are pivotal for cellular regulation and organization. Via adapting biological concepts, synthetic condensates with dynamic phase-separation control provide crucial insights into the fundamental cell processes and regulation of complex biological pathways.
View Article and Find Full Text PDFSoft Matter
December 2024
Institute for Molecules and Materials, Radboud University, Heyendaalseweg 135, 6523 AJ Nijmegen, The Netherlands.
Biomolecular condensates formed by liquid-liquid phase separation (LLPS) are important organizers of biochemistry in living cells. Condensate formation can be dynamically regulated, for example, by protein binding or enzymatic processes. However, how enzymatic reactions can influence condensate shape and control shape transformations is less well understood.
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