原细胞
凝聚
化学
分子
纳米技术
生物分子
生物发生
模块化设计
组合化学
小分子
分子识别
自然发生
生物物理学
相(物质)
分子间力
人工细胞
合成生物学
合成子
分子机器
生物结合
化学生物学
灵活性(工程)
固相合成
两亲分子
折叠(DSP实现)
联轴节(管道)
作者
Xiao-kun Zhang,Lingying Zhou,Lingyu Zhang,De‐Yi Wang,Xiaoyan Zheng,Ning Gao,Guangtao Li
标识
DOI:10.1002/ange.202519342
摘要
Abstract Although coacervates formed via liquid–liquid phase separation (LLPS) are widely considered plausible protocell models relevant to the origin of life, identifying minimalist, ultralow‐molecular‐weight molecules ( M w <300 Da) capable of undergoing LLPS remains a major challenge. Here we present a class of synthetic phase‐separating molecules with M w ranging from 211 to 215 Da–among the smallest known to drive coacervation. These molecules feature a modular design comprising a hydrophobic head and a hydrophilic tail, forming a minimalistic framework that significantly reduces molecular freedom and enables precise dissection of the fundamental interactions governing LLPS. Our findings reveal that LLPS is governed by a delicate balance between intermolecular non‐covalent interactions and molecular solvation. Furthermore, this molecular architecture serves as a versatile synthon for modularly constructing a range of task‐specific coacervates, including proton‐responsive, redox‐responsive, light‐responsive, and self‐fluorescent variants. These coacervates selectively accumulate diverse guest molecules and act as efficient bio‐crucibles that support key prebiotic processes, such as amino acid‐involved C─N coupling reactions, chiral catalysis, DNA hybridization, and energy transfer. These results provide both a molecular framework and chemical insights into the minimal requirements for LLPS, while advancing the coacervate toolkit for origins‐of‐life studies and synthetic cell engineering.
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