DNA
价
生物系统
溶解
膜
纳米技术
化学反应
DNA纳米技术
化学物理
计算机科学
生物物理学
化学
生物
生化工程
材料科学
哲学
生物化学
语言学
物理化学
工程类
作者
Siddharth Agarwal,Dino Osmanović,Mahdi Dizani,Melissa A. Klocke,Elisa Franco
标识
DOI:10.1038/s41467-024-46266-z
摘要
Artificial biomolecular condensates are emerging as a versatile approach to organize molecular targets and reactions without the need for lipid membranes. Here we ask whether the temporal response of artificial condensates can be controlled via designed chemical reactions. We address this general question by considering a model problem in which a phase separating component participates in reactions that dynamically activate or deactivate its ability to self-attract. Through a theoretical model we illustrate the transient and equilibrium effects of reactions, linking condensate response and reaction parameters. We experimentally realize our model problem using star-shaped DNA motifs known as nanostars to generate condensates, and we take advantage of strand invasion and displacement reactions to kinetically control the capacity of nanostars to interact. We demonstrate reversible dissolution and growth of DNA condensates in the presence of specific DNA inputs, and we characterize the role of toehold domains, nanostar size, and nanostar valency. Our results will support the development of artificial biomolecular condensates that can adapt to environmental changes with prescribed temporal dynamics.
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