Peters Elita, Tanase Diana A, Di Michele Lorenzo, Rubio-Sánchez Roger
Department of Chemical Engineering and Biotechnology, University of Cambridge, Philippa Fawcett Drive, Cambridge CB3 0AS, U.K.
Department of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.
J Am Chem Soc. 2025 Sep 17;147(37):33780-33789. doi: 10.1021/jacs.5c09928. Epub 2025 Sep 6.
Biological cells use cations as signaling messengers to regulate a variety of responses. Linking cations to the functionality of synthetic membranes is thus crucial to engineering advanced biomimetic agents such as synthetic cells. Here, we introduce bioinspired DNA-based receptors that exploit noncanonical G-quadruplexes for cation-actuated structural and functional responses in synthetic lipid membranes. Membrane confinement grants cation-dependent control over receptor assembly and, when supplemented with hemin cofactors, their peroxidase DNAzyme activity. Cation-mediated control extends to receptor lateral distribution to localize DNA-based catalysis within phase-separated membrane domains of model synthetic cells, imitating the localization of multimeric membrane complexes to signaling hubs in living cells. Our modular strategy paves the way for engineering from the bottom-up cation-responsive pathways for sensing, signaling, and communication in synthetic cellular systems.
生物细胞利用阳离子作为信号信使来调节各种反应。因此,将阳离子与合成膜的功能联系起来对于构建先进的仿生剂(如合成细胞)至关重要。在这里,我们引入了受生物启发的基于DNA的受体,该受体利用非经典G-四链体在合成脂质膜中实现阳离子驱动的结构和功能反应。膜限制赋予了对受体组装的阳离子依赖性控制,并且当补充血红素辅因子时,还赋予了它们的过氧化物酶DNAzyme活性。阳离子介导的控制扩展到受体的横向分布,以将基于DNA的催化定位在模型合成细胞的相分离膜域内,模仿多聚体膜复合物在活细胞中信号枢纽的定位。我们的模块化策略为在合成细胞系统中自下而上设计用于传感、信号传导和通信的阳离子响应途径铺平了道路。