A Pseudo-catalytic Network Motif for Thiol-based Chemical Reaction Networks

IF 3.1 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ekaterina A. Zhigileva, Ilia A. Puchkin, Sergey N. Semenov
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Abstract

The construction of chemical reaction networks (CRNs) is a formidable challenge because of their holistic and nonlinear nature. One approach to constructing CRNs involves combining fragments with distinctive properties, known as network motifs. Thiol chemistry is widely used in the construction of CRNs, with motifs available for positive and negative feedback loops. However, a simple catalytic motif has been lacking. Here, we developed a pseudo-catalytic motif using the reaction between cystamine and organic thiocyanates, which operates through a nucleophilic chain mechanism. Although similar to thiol autocatalytic systems, this reaction does not involve a doubling of the number of thiol species at any stage. The reaction is high-yielding and produces 2-amino-2-thiazoline. Its pseudo-catalytic nature manifests itself in the nearly linear relationship between the reaction rate and the amount of free thiols added at the beginning of the reaction. We demonstrated that this reaction can be regulated by external, time-dependent thiol signals and integrated into larger CRNs. We believe that this system will be a valuable addition to thiol chemistry, enabling the construction of CRNs with interesting functionalities.

Abstract Image

巯基化学反应网络的伪催化网络基序
化学反应网络具有整体性和非线性的特点,对化学反应网络的构建提出了严峻的挑战。构建crn的一种方法是将具有独特特性的片段(称为网络基序)组合在一起。巯基化学广泛应用于crn的构建,其基序可用于正反馈和负反馈回路。然而,一个简单的催化基序一直缺乏。在这里,我们开发了一个伪催化基序,利用半胺和有机硫氰酸酯之间的反应,通过亲核链机制运作。虽然与硫醇自催化系统相似,但该反应在任何阶段都不涉及硫醇种类数量的加倍。该反应产率高,可生产2-氨基-2-噻唑啉。它的准催化性质表现在反应速率与反应开始时加入的游离硫醇的量呈近似线性关系。我们证明了这种反应可以通过外部的、时变的硫醇信号来调节,并整合到更大的crn中。我们相信,该系统将成为硫醇化学的一个有价值的补充,使构建具有有趣功能的crn成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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