TY - JOUR
T1 - Protein coacervation-driven active forces power protocell dynamics
AU - Jia, Haiyang
AU - Sun, Huan
AU - Zhang, Weijie
AU - Ning, Xiao
AU - Mann, Stephen
N1 - Publisher Copyright:
© The Author(s) 2026.
PY - 2026/12
Y1 - 2026/12
N2 - Protein coacervates formed by liquid-liquid phase separation are emerging as active force generators, independent of ATP-driven motors. Nevertheless, the coordination and force scaling of protein coacervates remain largely unexplored. Here, we engineer a temperature-responsive elastin-based protocell model displaying temperature-modulated contractility and attendant force harnessing. By leveraging the phase separation properties, we modulate the protocell dynamics associated with volume contraction and membrane budding. Crosslinking of the elastin-based membrane influences the contraction dynamics such that the accumulation of mechanical forces in the protocells results in the spontaneous expulsion of internally trapped protein liquid-liquid phase separation (LLPS) complexes. We use a simple mathematically model to show how protein coacervation can amplify small piconewton-scale forces to perform large-scale mechanical work, highlighting the mechanical potential of protein coacervation dynamics. Taken together, our results provide a model framework for harnessing protein coacervates-driven forces and offer a step to future applications in synthetic biology, biomaterials and next-generation soft robotics.
AB - Protein coacervates formed by liquid-liquid phase separation are emerging as active force generators, independent of ATP-driven motors. Nevertheless, the coordination and force scaling of protein coacervates remain largely unexplored. Here, we engineer a temperature-responsive elastin-based protocell model displaying temperature-modulated contractility and attendant force harnessing. By leveraging the phase separation properties, we modulate the protocell dynamics associated with volume contraction and membrane budding. Crosslinking of the elastin-based membrane influences the contraction dynamics such that the accumulation of mechanical forces in the protocells results in the spontaneous expulsion of internally trapped protein liquid-liquid phase separation (LLPS) complexes. We use a simple mathematically model to show how protein coacervation can amplify small piconewton-scale forces to perform large-scale mechanical work, highlighting the mechanical potential of protein coacervation dynamics. Taken together, our results provide a model framework for harnessing protein coacervates-driven forces and offer a step to future applications in synthetic biology, biomaterials and next-generation soft robotics.
UR - https://www.scopus.com/pages/publications/105041077057
U2 - 10.1038/s41467-026-71593-8
DO - 10.1038/s41467-026-71593-8
M3 - Article
C2 - 41946707
AN - SCOPUS:105041077057
SN - 2041-1723
VL - 17
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 4935
ER -