Maity Indrajit, Wagner Nathaniel, Dev Dharm, Ashkenasy Gonen
Department of Chemistry, Ben-Gurion University of the Negev, Be'er Sheva 84105, Israel.
Acc Chem Res. 2025 Feb 4;58(3):428-439. doi: 10.1021/acs.accounts.4c00703. Epub 2025 Jan 22.
A key challenge in modern chemistry research is to mimic life-like functions using simple molecular networks and the integration of such networks into the first functional artificial cell. Central to this endeavor is the development of signaling elements that can regulate the cell function in time and space by producing entities of code with specific information to induce downstream activity. Such artificial signaling motifs can emerge in nonequilibrium systems, exhibiting complex dynamic behavior like bistability, multistability, oscillations, and chaos. However, the , bottom-up design of such systems remains challenging, primarily because the kinetic characteristics and energy aspects yielding bifurcation have not yet been globally defined. We herein review our recent work that focuses on the design and functional analysis of peptide-based networks, propelled by replication reactions and exhibiting bistable behavior. Furthermore, we rationalize and discuss their exploitation and implementation as variable signaling motifs in homogeneous and heterogeneous environments.The bistable reactions constitute reversible second-order autocatalysis as positive feedback to generate two distinct product distributions at steady state (SS), the low-SS and high-SS. Quantitative analyses reveal that a phase transition from simple reversible equilibration dynamics into bistability takes place when the system is continuously fueled, using a reducing agent, to keep it far from equilibrium. In addition, an extensive set of experimental, theoretical, and simulation studies highlight a defined parameter space where bistability operates.Analogous to the arrangement of protein-based bistable motifs in intracellular signaling pathways, sequential concatenation of the synthetic bistable networks is used for signal processing in homogeneous media. The cascaded network output signals are switched and erased or transduced by manipulating the order of addition of the components, allowing it to reach "on demand" either the low-SS or high-SS. The pre-encoded bistable networks are also useful as a programming tool for the downstream regulation of nanoscale materials properties, bridging together the Systems Chemistry and Nanotechnology fields. In such heterogeneous cascade pathways, the outputs of the bistable network serve as input signals for consecutive nanoparticle formation reaction and growth processes, which-depending on the applied conditions-regulate various features of (Au) nanoparticle shape and assembly.Our work enables the design and production of various signaling apparatus that feature higher complexity than previously observed in chemical networks. Future studies, briefly discussed at the end of the Account, will be directed at the design and analysis of more elaborate functionality, such as bistability under flow conditions, multistability, and oscillations. We propose that a profound understanding of the design principles facilitating the replication-based bistability and related functions bear implications for exploring the origin of protein functionality prior to the highly evolved replication-translation-transcription machinery. The integration of our peptide-based signaling motifs within future synthetic cells seems to be a straightforward development of the two alternating states as memory and switch elements for controlling cell growth and division and even communication among different cells. We furthermore suggest that such systems can be introduced into living cells for various biotechnology applications, such as switches for cell temporal and spatial manipulations.
现代化学研究中的一个关键挑战是利用简单的分子网络模拟类似生命的功能,并将此类网络整合到首个功能性人工细胞中。这一努力的核心是开发信号元件,这些元件可以通过产生具有特定信息的编码实体来诱导下游活性,从而在时间和空间上调节细胞功能。这种人工信号基序可以在非平衡系统中出现,表现出诸如双稳性、多稳性、振荡和混沌等复杂的动态行为。然而,此类系统的自下而上设计仍然具有挑战性,主要是因为产生分岔的动力学特征和能量方面尚未得到全面定义。我们在此回顾我们最近的工作,该工作专注于基于肽的网络的设计和功能分析,这些网络由复制反应推动并表现出双稳行为。此外,我们对其作为均相和异相环境中可变信号基序的开发和实施进行了合理化分析和讨论。双稳反应构成可逆的二级自催化,作为正反馈以在稳态(SS)下产生两种不同的产物分布,即低稳态和高稳态。定量分析表明,当使用还原剂持续为系统提供能量以使其远离平衡时,系统会从简单的可逆平衡动力学发生相变进入双稳状态。此外,大量的实验、理论和模拟研究突出了双稳性起作用的特定参数空间。类似于细胞内信号通路中基于蛋白质的双稳基序的排列,合成双稳网络的顺序串联用于均相介质中的信号处理。通过操纵组分添加顺序,可以切换、擦除或转导级联网络输出信号,使其能够“按需”达到低稳态或高稳态。预编码的双稳网络还可用作纳米级材料特性下游调控的编程工具,将系统化学和纳米技术领域联系起来。在这种异相级联途径中,双稳网络的输出作为连续纳米颗粒形成反应和生长过程的输入信号,这取决于应用条件,调节(金)纳米颗粒形状和组装的各种特征。我们的工作能够设计和生产各种信号装置,其复杂性高于先前在化学网络中观察到的。在本综述结尾简要讨论的未来研究将针对更精细功能的设计和分析,如流动条件下的双稳性、多稳性和振荡。我们提出,深入理解促进基于复制的双稳性及相关功能的设计原则,对于在高度进化的复制 - 翻译 - 转录机制之前探索蛋白质功能的起源具有重要意义。将我们基于肽的信号基序整合到未来的合成细胞中,似乎是将这两种交替状态直接发展为用于控制细胞生长和分裂甚至不同细胞间通信的记忆和开关元件。我们还建议,可以将此类系统引入活细胞用于各种生物技术应用,如细胞时空操纵的开关。