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碳二亚胺引发的催化反应循环调控超分子过程。

Carbodiimide-fueled catalytic reaction cycles to regulate supramolecular processes.

机构信息

Department of Chemistry, Technical University of Munich, Lichtenbergstraße 4, 85748 Garching, Germany.

Institute for Advanced Study, Technical University of Munich, Lichtenbergstraße 2a, 85748, Garching, Germany.

出版信息

Chem Commun (Camb). 2022 Jan 27;58(9):1284-1297. doi: 10.1039/d1cc06428b.

Abstract

Using molecular self-assembly, supramolecular chemists can create Gigadalton-structures with angstrom precision held together by non-covalent interactions. However, despite relying on the same molecular toolbox for self-assembly, these synthetic structures lack the complexity and sophistication of biological assemblies. Those assemblies are non-equilibrium structures that rely on the constant consumption of energy transduced from the hydrolysis of chemical fuels like ATP and GTP, which endows them with dynamic properties, , temporal and spatial control and self-healing ability. Thus, to synthesize life-like materials, we have to find a reaction cycle that converts chemical energy to regulate self-assembly. We and others recently found that this can be done by a reaction cycle that hydrates carbodiimides. This feature article aims to provide an overview of how the energy transduced from carbodiimide hydration can alter the function of molecules and regulate molecular assemblies. The goal is to offer the reader design considerations for carbodiimide-driven reaction cycles to create a desired morphology or function of the assembly and ultimately to push chemically fueled self-assembly further towards the bottom-up synthesis of life.

摘要

利用分子自组装,超分子化学家可以创造出具有埃精度的吉加达尔顿结构,这些结构由非共价相互作用连接在一起。然而,尽管这些合成结构依赖于相同的分子工具箱进行自组装,但它们缺乏生物组装的复杂性和复杂性。这些组装是依赖于从 ATP 和 GTP 等化学燃料水解中转化而来的能量不断消耗的非平衡结构,这赋予了它们动态特性、时空控制和自我修复能力。因此,要合成类生命材料,我们必须找到一个将化学能转化为自我组装的反应循环。我们和其他人最近发现,这可以通过一个水合碳二亚胺的反应循环来实现。本文的目的是概述从碳二亚胺水合作用中传递的能量如何改变分子的功能并调节分子组装。目标是为读者提供关于碳二亚胺驱动的反应循环的设计考虑因素,以创建所需的组装形貌或功能,并最终将化学燃料驱动的自组装进一步推向生命的自下而上合成。

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