Liu Wei, Deng Jie, Song Siyu, Sethi Soumya, Walther Andreas
Life-Like Materials and Systems, Department of Chemistry, University of Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Luoyu Road 1037, 430074, Wuhan, China.
Commun Chem. 2024 May 1;7(1):100. doi: 10.1038/s42004-024-01185-4.
Biomolecular coacervates are emerging models to understand biological systems and important building blocks for designer applications. DNA can be used to build up programmable coacervates, but often the processes and building blocks to make those are only available to specialists. Here, we report a simple approach for the formation of dynamic, multivalency-driven coacervates using long single-stranded DNA homopolymer in combination with a series of palindromic binders to serve as a synthetic coacervate droplet. We reveal details on how the length and sequence of the multivalent binders influence coacervate formation, how to introduce switching and autonomous behavior in reaction circuits, as well as how to engineer wetting, engulfment and fusion in multi-coacervate system. Our simple-to-use model DNA coacervates enhance the understanding of coacervate dynamics, fusion, phase transition mechanisms, and wetting behavior between coacervates, forming a solid foundation for the development of innovative synthetic and programmable coacervates for fundamental studies and applications.
生物分子凝聚体是理解生物系统的新兴模型,也是用于设计应用的重要构建模块。DNA可用于构建可编程凝聚体,但通常制备这些凝聚体的过程和构建模块只有专家才能掌握。在此,我们报告了一种简单的方法,使用长单链DNA同聚物与一系列回文结合剂相结合,形成动态的、多价驱动的凝聚体,作为合成凝聚体微滴。我们揭示了多价结合剂的长度和序列如何影响凝聚体形成、如何在反应回路中引入切换和自主行为,以及如何在多凝聚体系统中设计润湿性、吞噬和融合。我们这种易于使用的模型DNA凝聚体增进了对凝聚体动力学、融合、相变机制以及凝聚体之间润湿性的理解,为开发用于基础研究和应用的创新合成和可编程凝聚体奠定了坚实基础。