| Literature DB >> 28892230 |
Dávid Komáromy1, Meniz Tezcan1, Gaël Schaeffer1, Ivana Marić1, Sijbren Otto1.
Abstract
In living systems processes like genome duplication and cell division are carefully synchronized through subsystem coupling. If we are to create life de novo, similar control over essential processes such as self-replication need to be developed. Here we report that coupling two dynamic combinatorial subsystems, featuring two separate building blocks, enables effector-mediated control over self-replication. The subsystem based on the first building block shows only self-replication, whereas that based on the second one is solely responsive toward a specific external effector molecule. Mixing the subsystems arrests replication until the effector molecule is added, resulting in the formation of a host-effector complex and the liberation of the building block that subsequently engages in self-replication. The onset, rate and extent of self-replication is controlled by the amount of effector present.Keywords: dynamic combinatorial chemistry; host-guest chemistry; molecular networks; self-replication; systems chemistry
Year: 2017 PMID: 28892230 DOI: 10.1002/anie.201707191
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336