Andersen Dante Guldbrandsen, Pedersen Andreas Bøtker, Jørgensen Martin Høgholm, Montasell Mireia Casanovas, Søgaard Ane Bretschneider, Chen Gal, Schroeder Avi, Andersen Gregers Rom, Zelikin Alexander N
iNano Interdisciplinary Nanoscience Center, Aarhus University, Aarhus, 8000, Denmark.
Department of Chemistry, Aarhus University, Aarhus, 8000, Denmark.
Adv Mater. 2024 Feb;36(6):e2309385. doi: 10.1002/adma.202309385. Epub 2023 Dec 6.
In this work, synthetic cells equipped with an artificial signaling pathway that connects an extracellular trigger event to the activation of intracellular transcription are engineered. Learning from nature, this is done via an engineering of responsive enzymes, such that activation of enzymatic activity can be triggered by an external biochemical stimulus. Reversibly deactivated creatine kinase to achieve triggered production of adenosine triphosphate, and a reversibly deactivated nucleic acid polymerase for on-demand synthesis of RNA are engineered. An extracellular, enzyme-activated production of a diffusible zymogen activator is also designed. The key achievement of this work is that the importance of cellularity is illustrated whereby the separation of biochemical partners is essential to resolve their incompatibility, to enable transcription within the confines of a synthetic cell. The herein designed biochemical pathway and the engineered synthetic cells are arguably primitive compared to their natural counterpart. Nevertheless, the results present a significant step toward the design of synthetic cells with responsive behavior, en route from abiotic to life-like cell mimics.
在这项工作中,设计了配备人工信号通路的合成细胞,该通路将细胞外触发事件与细胞内转录激活相连接。借鉴自然,这是通过对响应性酶进行工程改造来实现的,使得酶活性的激活可以由外部生化刺激触发。设计了可逆失活的肌酸激酶以实现三磷酸腺苷的触发产生,以及用于按需合成RNA的可逆失活的核酸聚合酶。还设计了一种细胞外酶激活的可扩散酶原激活剂的产生。这项工作的关键成果在于说明了细胞性的重要性,即生化伙伴的分离对于解决它们的不相容性、在合成细胞范围内实现转录至关重要。与天然细胞相比,本文设计的生化途径和工程化合成细胞可以说是原始的。然而,这些结果朝着设计具有响应行为的合成细胞迈出了重要一步,是从非生物到类生命细胞模拟物的过程中的一步。