Chemically Programmable Liquid-to-Solid Transitions and Spatial Dynamics in Synthetic Coacervates
- 1 July 2026
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 148 (27) , 29220-29230
Abstract
Biomolecular condensates undergo dynamic maturation, transitioning from liquid-like droplets to gel-like or solid-like assemblies, exhibiting structural heterogeneity in response to biochemical cues. Synthetic coacervate droplets formed via liquid-liquid phase separation (LLPS) have emerged as simplified models of these condensates and of protocells. Yet, the understanding of complex phase behaviors of liquid-like droplets in both biological and chemical contexts remains less explored, limiting our understanding of biological function and the design of droplet-based soft materials and protocells. Here, we introduce a chemically programmable strategy to dynamically modulate droplet phase transitions through controlled polymer-network cross-linking. Reactive cross-linkers selectively engage polymers within liquid-like droplets, progressively increasing internal microviscosity and inducing a liquid-to-solid transition. Beyond uniform phase regulation, network cross-linking drives spatially heterogeneous phase separation via polymer demixing and Ostwald ripening, with reaction-diffusion dynamics critically shaping both thermodynamically stable and metastable droplets. Using orthogonal cleavable cross-linkers, we further demonstrate chemical control over droplet liquefaction and the generation of multiphasic structures with pathway-dependent configurations. Integration of photoresponsive cross-linkers with digital-micromirror device (DMD) technology enables precise spatial photopatterning of droplet networks. This work establishes a versatile framework for elucidating the structural principles of microphase separation within coacervates and provides a blueprint for designing dynamic soft materials and synthetic protocells.Keywords
Funding Information
- Beijing-Tianjin-Hebei Natural Science Foundation Cooperation Project (25JJJJC0025)
- Interdisciplinary Research Center of Beijing University of Chemical Technology (XK2025-05)
- National Natural Science Foundation of China (22572006)
- National Natural Science Foundation of China (52221006)
This publication has 64 references indexed in Scilit:
- Tailoring Multiphasic Protein Condensates via Liquid‐Liquid Phase SeparationAggregate, 2026
- Programmable Dimensional Lithography with Digital Micromirror Devices for Multifunctional MicroarchitecturesAdvanced Materials Technologies, 2025
- Light‐Responsive DNA Droplets for Controlling Enzyme Cascade Pathways by Dynamic Phase SeparationAngewandte Chemie International Edition, 2025
- Catalytically Active Coacervates Sustained Out‐of‐EquilibriumAngewandte Chemie International Edition, 2025
- Supramolecular Switching of Liquid‐Liquid Phase Separation for Orchestrating Enzyme KineticsAngewandte Chemie International Edition, 2025
- Photochemically Triggered and Autonomous Oscillatory pH‐Modulated Transient Assembly/Disassembly of DNA Microdroplet CoacervatesAngewandte Chemie International Edition, 2024
- Dynamical Behaviors of Oscillating Metallosurfactant Coacervate Microdroplets under Redox StressAdvanced Materials, 2023
- Bio‐inspired functional coacervatesAggregate, 2022
- Small‐Molecule‐based Supramolecular Plastics Mediated by Liquid‐Liquid Phase Separation**Angewandte Chemie International Edition, 2022
- Optothermally Programmable Liquids with Spatiotemporal Precision and Functional ComplexityAdvanced Materials, 2022