Chemical Zymogens and Transmembrane Activation of Transcription in Synthetic Cells

© 2023 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 6 vom: 15. Feb., Seite e2309385
1. Verfasser: Andersen, Dante Guldbrandsen (VerfasserIn)
Weitere Verfasser: Pedersen, Andreas Bøtker, Jørgensen, Martin Høgholm, Montasell, Mireia Casanovas, Søgaard, Ane Bretschneider, Chen, Gal, Schroeder, Avi, Andersen, Gregers Rom, Zelikin, Alexander N
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article chemical zymogen enzyme activation synthetic cells transcription Enzyme Precursors
Beschreibung
Zusammenfassung:© 2023 Wiley-VCH GmbH.
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
Beschreibung:Date Completed 14.02.2024
Date Revised 14.02.2024
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202309385