Tuning the Kinetic Trapping in Chemically Fueled Self-Assembly**

IF 3.1 Q2 CHEMISTRY, MULTIDISCIPLINARY ChemSystemsChem Pub Date : 2022-10-06 DOI:10.1002/syst.202200035
Brigitte A. K. Kriebisch, Christine M. E. Kriebisch, Alexander M. Bergmann, Dr. Caren Wanzke, Dr. Marta Tena-Solsona, Prof. Dr. Job Boekhoven
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引用次数: 3

Abstract

Nature uses dynamic, molecular self-assembly to create cellular architectures that adapt to their environment. For example, a guanosine triphosphate (GTP)-driven reaction cycle activates and deactivates tubulin for dynamic assembly into microtubules. Inspired by dynamic self-assembly in biology, recent studies have developed synthetic analogs of assemblies regulated by chemically fueled reaction cycles. A challenge in these studies is to control the interplay between rapid disassembly and kinetic trapping of building blocks known as dynamic instabilities. In this work, we show how molecular design can tune the tendency of molecules to remain trapped in their assembly. We show how that design can alter the dynamic of emerging assemblies. Our work should give design rules for approaching dynamic instabilities in chemically fueled assemblies to create new adaptive nanotechnologies.

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调整化学燃料自组装中的动力学捕获
大自然利用动态的分子自组装来创造适应环境的细胞结构。例如,三磷酸鸟苷(GTP)驱动的反应循环激活和灭活微管蛋白,以便动态组装成微管。受生物学中动态自组装的启发,最近的研究开发了由化学燃料反应周期调节的组装的合成类似物。这些研究中的一个挑战是如何控制快速拆卸和动态捕获之间的相互作用,即动态不稳定性。在这项工作中,我们展示了分子设计如何调整分子在其组装中保持被困的趋势。我们展示了这种设计如何改变新兴组件的动态。我们的工作应该为接近化学燃料组件的动态不稳定性提供设计规则,以创建新的自适应纳米技术。
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